clinical research courses in bangalore

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• Certification in Clinical Research
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Accreditations.

Accredited by the International Accreditation Organization (IAO), the Life Science Sector Skills Development Council (LSSSDC), and the National Skill Development Council (NSDC).

Job Oriented Programs

Get comprehensive job-oriented programs to empower you with the skills and knowledge you need to succeed in the dynamic and competitive healthcare sector.

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Equip yourself with skills and knowledge under the mentorship of experienced faculties with over 17 years of experience in the field of healthcare research and training.

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CliniLaunch offers 0% interest for education loans to significantly reduce the financial burden and let you focus on your studies rather than thinking about debt accumulation.

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Strong network of recruiters from the healthcare, pharmaceutical, and biotechnology industries and offer placement assistance to students.

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Hear From Our Students

SUBIYA got placed in INFORMATION TECHNOLOGY AND SERVICES after completing her Clinical Research course from CLRI- Clinilaunch Research Institute.

PRATHAMESH got placed in INFORMATION TECHNOLOGY AND SERVICES. after completing her Medical Coding course from CLRI- Clinilaunch Research Institute.

SAMRUDDHI got placed in I,SHNOVA after completing her Clinical Research course from CLRI- Clinilaunch Research Institute.

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I really enjoyed learning at Clinilaunch. The teachers are amazing and very supportive. Everyone helped me a lot from the start until I got a great job. A big thank you to the teachers, the team behind the scenes, the HR folks, and the leaders for making my learning journey smooth and rewarding.

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Bangalore head office

46/4, Hosur Rd, Kudlu Gate, Krishna Reddy Industrial Area, H.S, R Extension, Bengaluru, Karnataka 560068

Bangalore branch

B, 90, 1st C Main Rd, Jakkasandra, 1st Block Koramangala, Koramangala, Bengaluru, Karnataka 560034

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• New PGDCR Online/offline Batch Announcement-3rd Sept 2024 Hurry up and few seats left Weekdays classes 1 hour per day Interested candidates can enroll...
• New offline/Online batches for CDM/PV and SAS from 3rd September 2024 Starting from 3rd September 2024 . Limited Seats, Hurry Up!!!...

KCRI established in year 2008 under the guidance of Leaders and iexperts in the field of Clinical Research.The company itself dreamed to educate the Life science graduate the core of Clinical Research .

• We work as the bridge between Education life and Corporate or professional life of any candidate.
• Here in KCRI we make sure that the candidate is getting right education as per his/her academics.
• Since 2008 we have taught more than 10000 candidates and we have the record of best placements in the industry till now.
• We believe that along with the academics a candidate should be job ready also, So to fulfil this requirement we groom the candidate 360 degree.
• We assess, analyse and then suggest the training to the candidate.
• KCRI has been teaching the different courses under Clinical Research.

• PGDCR is the course which I took, I learnt during training and also during internship.Training, hands on practical, mock test, preparation for interview and trainer’s support. KCRI given me 3… Rajath
• I come from BDS background and was worried about job after the training, The medical writing suggestion given by the management of KCRI worked for me, Now I am working… Kavya
• I was searching a good institute to learn Clinical Research, I found few names. In those few were offering  PG Diploma for very high fee, it was not affordable to… Ratna

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PG Diploma in Clinical Research

• PG Diploma in CDM
• Adv. PG Diploma in Clinical Research
• Certification in Clinical Research
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Welcome to Avigna Clinical Research Institute – ACRI

Join the 100% recession proof industry, classroom training.

Enhance your skills from the comfort of your home

VIRTUAL LEARNING

Certification in Clinical Research is awarded

ONLINE TRAINING

1200+ ACRI Trained Professionals

Real Time Experience in PV Software

Mock Interview Training

50+ Placement Partners

100% Placement & Internship Assistance Guaranteed

*Conditions Apply

About Avigna Clinical Research Institute

Avigna Clinical Research Institute (ACRI) is one of the most premier Clinical Research institutes of India, dedicated to providing excellent Clinical Research Professionals to its field. Numerous students and professionals from Allied Health Science/Life Science streams have benefited from our robust curriculum, coupled with training in soft skills and internships in leading Clinical Research Organizations.

ELIGIBILITY FOR COURSE: B.Sc/M.Sc ( Botany, Zoology, Chemistry, Biochemistry, Biotechnology, Microbiology, Genetics, Nursing), B.Tech (Biotechnology), M.B.B.S / B.D.S / B.A.M.S / B.H.M.S / B.V.Sc. / B.S.M.S, B.Pharm / M.Pharm. This course is best suited for Freshers/Mid-term career change/Better career growth.

COURSE OUTCOMES: PG Diploma Clinical Research in Bangalore is awarded to candidates who take up Classroom or Virtual Training. Certification in Clinical Research is awarded to candidates who take up our online clinical research courses in Bangalore .

PLACEMENT & INTERNSHIP ASSISTANCE GUARANTEED 100% Placement & Internship Assistance Guaranteed. *Conditions Apply After the training, we arrange interviews with the employers. We provide interview support to the student till the time they are placed. Internships are provided to the fresh graduates after completion of the 3 months class room program.

MARKET LEADERS IN INNOVATION

We are clearly the market leaders in terms of our self-designed, up-to-date industry-integrated curriculum, as well as the technical and soft skills we impart our students, while making them adept at the use of modern technology.

BEST PLACEMENT RECORD IN THE INDUSTRY

Our commitment to our students does not just end with providing them the best skills and training possible, but also to helping them start their career with the best names in the industry. No wonder, we have the best placement record for Clinical Research professionals and our previous batch students are placed with top CROs, Pharmaceuticals and Bio-tech companies.

THE ACRI CULTURE OF GROWTH

At ACRI, one of the top clinical research institutes in Bangalore , we have established a culture of constant growth, innovation and enterprise in a professional environment aided with state-of-the-art facilities, led by our supportive staff who teach professionally every aspect of online clinical research courses in Bangalore .

Join our 1200+ ACRIDIANS working in the CLINICAL RESEARCH space since 2010!

• Read Full Review...

Review & Placements

Student’s reviews, dr. shruthi b r.

After learning about the scope of clinical research, I wanted to pursue a course in the same. The next very big question was pursue from where? And I landed here at ACRI. IT is indeed the best institute. The faculties here are excellent and always approachable, so are the supporting staff. A dedicated team for assisting in placements. Through ACRI I got opportunity to interview with leading companies and am placed in a leading pharmaceutical company as a Drug safety Associate. All credits to the entire team of ACRI. Kudos!

PURNIMA H.D

ACRI is the best institute where i got a thorough knowledge about clinical research. I joined ACRI in July 2018. I had a great experience where i gained a depth knowledge about clinical research and developed my skills. The technical sessions and the PD sessions were excellent and very much helpful. The faculties are really best and supportive. The placement assistance is very good. I have got placed in IQVIA. My sincere thanks to all the faculties of ACRI for being so supportive and guiding me to develop my career in clinical research. I am very much thankful to be a part of ACRI. Whoever wants to develop a career in Clinical Research, ACRI is the best place to learn and develop your skills. It was really worth choosing this institute to start my career in clinical research.

Best institute to enhance your knowledge in Clinical Research. The three months course at ACRI has been a great experience. The four modules taken up was wonderfully taught by the Mentors and all the Mentors are friendly and really supportive. The personality development sessions were conducted wherein we had group discussions, pick and speak, role plays, essay writing which helped us gain confidence and build up soft skills. The aptitude tests, gave an idea so as how to solve tricky maths and comprehensive passages which has helped me clear the aptitude test in the Interviews. Good placement assistance was provided by the Institute. I’ve been recently placed in one of the leading CRO’s, Parexel as an Associate Clinical Data Analyst. ACRI has given me the best learning experience and I would suggest all the aspirants looking for career in Clinical Research to take up the course here.

Dr. ANUPAMA HOSMATH

One of the best institute in Bangalore for Clinical Research training. The course at ACRI is comprehensive and affordable. ACRI has a dedicated staff for training. The study material and conduct of classes is very regular and prompt. Strict assessment after every module has helped me a lot to gain my confidence in attending interview. ACRI has the best placement assistance, gives opportunity to attend interviews in best of the companies. I recently got placed with good package and ACRI has been a great support in this regard. Before joining ACRI, I visited couple of clinical research institutes wherein I could hardly see any infrastructure or training staff present at the time of my visit. I highly recommend ACRI for candidates who aspire to pursue their career in clinical research

SREELAKSHMI SATHYAKUMAR

I joined Avigna Clinical Research Institute after I completed my Graduation in B.E Biotechnology. I felt the immense need of having technical knowledge prior to joining an industry. Hence i Joined the PG Diploma course in Clinical research. The classes were very interesting and informative. All the trainers helped me gain extra knowledge and with the placement support I am successfully placed in ACCENTURE.

I thank everyone in the institution for helping me pursue my goals.

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Frequently Asked Questions

Who are the key employers.

We are actively networked with over 100 employers both Indian and multi-national companies.

Are there any overseas job opportunities?

Yes, once you acquire experience in India, you could explore international opportunities. You must ensure that you qualify the immigration criteria...

Can final year students apply for this course?

Yes, final year students can apply and join the program. However, you need to produce your result/degree/course completion certificate...

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Cliniminds -, (19+ years now), contact : +91-9902261347, lsssdc live elearning pg diploma, fulltime - 4 months live elearning, weekend - 6 months live elearning, 9500+ cliniminds alumni, eligibility - b.pharmacy, m.pharmacy, doctor of pharmacy, bsc, msc, bds, bhms, bams, b.tech / m.tech biotech, biomedical, life sciences., recent placements, program inclusions.

• Live Interactive eLearning Sessions
• Hands on Software Training - Pharmacovigilance Safety Database, Clinical Data Management, eCTD Software.
• Arranging Job Interviews - Campus Placements.
• Dedicated Placement Cell - 360° Placement Support.
• Pre Placement Training - CV Writing, Mock Interviews, English Communication, Aptitude Test Training
• Access to LMS – 24x7 - Recordings, PPT, Notes, eBooks.

Certifications

• 1 Life Sciences Sector Skill Development Council, NCVET.
• 2 Advanced PG Diploma – Cliniminds - Program Accredited by Accreditation Council for Clinical Research Education, United States of America.
• 3 Internship Certification – www.thinki.in
• 4 ICH GCP Certificate – Cliniminds

Clinical Research Modules

• Drug Discovery
• Overview of Clinical Research
• Regulations & Guidelines in Clinical Research
• Roles & Responsibilities of Key Stakeholders
• Preparation & Planning of Clinical Trials
• Essential Documentation in Clinical Research & Regulatory Submission
• Study Start Up Process
• Clinical Monitoring Essentials
• Compliance, Auditing & Quality Control in Clinical Research

Pharmacovigilance Modules

• Pharmacology – General Principles
• Introduction to Pharmacovigilance
• Pharmacovigilance Regulations
• Hands on Training on Case Processing and Report Generation
• Safety Reporting and Processing ICSR
• Aggregate Reports, Signal Detection & Risk Management
• Documents in Pharmacovigilance
• Audits & Inspections
• Advanced Pharmacovigilance & Analytics

Clinical Data Management Modules

• Overview of Clinical Data Management
• Clinical Data Integrity
• Data Management Plan
• Design of Case Report Form
• CRF Tracking
• Electronic Data Capture
• Data Entry Guidelines
• Edit Check Creation, Validation, Programming
• Discrepancy Management
• Data Transfer in Clinical Data Management
• Medical Coding Dictionaries
• Laboratory Test in Clinical Trials
• Creating Reports
• Adverse Event Reporting & Reconciliation
• Audit Trail
• Database Lock
• Quality Assurance in Clinical Data Management
• QMS, Audit & Inspection, SOP Compliance
• Hands on Software Training

Drug Regulatory Affairs, IPR/ Patents

• Drug Development Process & Introduction to Clinical Research
• Introduction to Regulatory Affairs, Terms & Terminologies & Abbreviations
• Chemistry, Manufacturing & Controls (CMC)
• Drug Master File
• Regulatory, Filing System for DMF in Different Countries
• ICH – Introduction, Objectives & Guidelines
• CTD Introduction - Module 1 to 5
• Regulatory Filing Systems in Europe
• Regulatory Filing Systems in US
• Registration Procedures in Rest of the World
• Validations
• Audits & Compliances
• Regulatory Operations
• Pre Publishing
• Final Submission via Gateways
• Practical Approach towards Overall Dossier Preparation & Submission
• Indian Pharmaceutical Regulations
• Introduction to Patent Regime
• Introduction to Patents
• Industrial designs
• Trade Secrets
• Geographical indications
• Types of Patent
• Patentability criteria
• Patentable subject matter/Non Patentable subject matter
• Anatomy of Patent
• Term of a Patent Expiry calculation of patents.
• Inventor ship
• Duty of Disclosure
• Types of Searches
• Various Search Engines
• Performing a Search (Dummy Strategy) & Advantages of patent search
• International Patent classification Patent
• Introduction to patent drafting
• Specification and Description
• Written description, Enablement and Best mode requirement

Clinical SAS Modules

• SAS Introduction
• Infile option
• Methods to read data
• Import Export of data
• Set and where statements
• If then Else statement
• If then and Loop
• Addition of data
• Merging of data
• Functions in SAS
• Procedures in SAS
• SQL Overview
• Macro Overview
• ODS(Output Delivery System)

ADVANCED (CDISC) SAS

• Introduction to CDISC
• Overview of CT Protocol, SAP, CRF, TFL shell
• Sample CRF Annotation activity
• Overview of SDTM Implementation guide
• Overview of ADaM Implementation guide
• Preparation of Dataset specification (SDTM + ADaM)
• Sample SDTM creation
• Sample ADaM creation
• Creation of .XPT files for Regulatory submission
• Sample TFLs creation
• Overview of P21 tool for validation of data
• Overview of University free SAS version usage to perform above
• activities on dummy project
• Overview of define.xml and final regulatory submission package

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For more information, please contact: Cliniminds Bengaluru +91-9902261347   , +91-9560102589 , +91-9810068241   C/O BHIVE Workspace Platinum Indiranagar, 271, 6th Main Rd, HAL 2nd Stage, Motappapalya, Indiranagar, Bengaluru, Karnataka 560038 Email us your queries : [email protected]

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Online Clinical Research Course Training

Live lectures, lms access and placement support, quick query, our students, our pride.

Advance Program in Clinical Research & Management (APCRM)

• B.Pharm/ M.Pharm/Pharm.D
• B.Sc/ M.Sc/ PhD Life Sciences/ Chemistry
• MBBS/BDS/BAMS/BHMS etc.
• BPT/MPT etc
• Clinical Operations
• Clinical Data Management
• Pharmacovigilance
• Medical Writing
• Soft Skills/ Communication Skills Classes

Clinical Research Course from India's Leading Training Institute

Learn Clinical Research Course Online with Regular (Weekdays) and Part-time(Weekend) Career-oriented clinical research training with Live Lectures and LMS Access. Learn Clinical Research, Clinical Data Management (CDM), Pharmacovigilance (PV), and Medical Writing.

We offer different types of Courses in Clinical Research, Courses after M.Sc. And courses after B Pharma, M Pharma, D Pharma - Online Clinical Research Courses, Pharmacy Course, part-time and, full-time courses in clinical research. Clini India is one of the top Clinical Research Training Institutes in Hyderabad, Bangalore, Pune, and Mumbai offer online clinical research courses in Clinical Data Management, Medical Writing, and Pharmacovigilance Courses Online.

Certification in Pharmacovigilance, Medical writing, Clinical data Management & clinical research. Learn From online or offline, Flexible Classes, training with placement assistance

Why Choose Clini India

• India’s Most Trusted Clinical Research Training Institute

Best Placements

Iso 9001:2015 certified, lms access with video & clinical research industry interview preparations., assignments with case study based learning.

Pre-Recruitment Trainings

Mock interview & mock exams exam.cliniindia.com, award winning institute (education excellence award) for best clinical research institute, exclusive career support and guidance cell.

Our Program Features

• ISO 9001:2015 Clinical Research Training Institute
• Gain Industry endorsed Clinical Research Certification.
• Industry Mentors from leading CRO and Pharma Companies
• Best Clinical Research Institute in India with Soft skills Training and Placement Assistance
• Hands on Training on Clinical Data Management and Pharmacovigilance Tools

Join Online Clinical Research Course

Join Award Winning Clinical Research Training Course, learn about Pharmacovigilance Course, Medical Writing Course, Clinical Research Course, GCP Course online & Clinical Data Management Course for Life Science Pharmacy Students, with LIVE Online Classes and LMS Access. Thousands of Students have been successfully placed in leading CRO’s, pharma, and IT companies. Best Institute for Clinical Research Curses with 100% Placement.LMS Access to Live Classes.

Grab an opportunity to grab 100% Placement support. Learn from Leading Industry Experts from Contract Research Organizations, Pharmacovigilance, Information Technology Organizations etc. Pharma and Life Science (Biotech, Microbiology, Biochemistry) students who studied from Clini India are working with Leading Clinical Research Organizations, Pharma and IT Companies.

APCRM Covers- Clinical Research, Pharmacovigilance, Clinical Data Management, Drug Safety and Medical Writing.

Want to know more about Clini India

What our students say

My experience with cliniindia has been amazing. I would like to extend my gratitude to my coordinator kranti maam who has always extended a helping hand . Today I am placed in GSK and that too within 2 months of joining the course , and that would not have been possible without kranti maam's help and support. Cliniindia has truly given a new start to my career

Clini India One of the Best Institute in India. After completing my Master's I had joined this institute and this helped me to get placed. Best faculties are there who had clear all my doubts and helped me to get more knowledge about CDM and clinical research and clinical trials and Medical writing. Really I would suggest everyone to join this institute

It is a good place to join for those looking for a bright career in clinical research and Pharmacovigilance. All the staffs are helpful especially Mr.Lokesh. All the classes are very detailed and informative with detailed PowerPoint presentation. Classes by Paramita Saha Maam is very crisp and detailed. This institution provides placement even during lockdown

I joined Clini India in between my job. I wanted to start a career in clinical research, so I inquired about few institutes, I came to know about Clini through one of my friends. Furthermore, I joined the weekend batch and the classes were conducted every Sunday. The trainers are supportive and helpful. I got placed in one of the upcoming CRO immediately after completion of my course. It was a great experience overall

I had joined the August 2020 online batch, so far all the explanations' about various topics from the expertise is thoroughly cleared. I would definitely recommend Clini India for the aspirants who want to make a great career in clinical research

Potential Employers for your Career

--> SAS Accredited Institute

• Latest and Updated Study Content from SAS, as required by employers
• Earn genuine DIGITAL Badges
• SAS Certification attempt Included in the course
• Learn from SAS authorized Trainers
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• Listing on an exclusive career portal to direct connect with SAS Employers
• Resume writing tips to help you get hired and much more.

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Select Qualification B.Pharm M.Pharm Pharm.D M.Sc B.Sc BDS MBBS BHMS BAMS BE B.Tech Others

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Advanced Program in Clinical Research and Management (APCRM)

Need help? Contact our support team Tell us about your query…

Join our community of learners and elevate your career in clinical research.

Year of Completion Prior to 2020 2021 2022 2023 2024

Preferred e-Campus Bangalore Pune Hyderabad Mumbai Delhi/Noida

Latest Updates

Admissions Open for APCRM Programs..

CLINI INDIA provides hands on Training Program on Pharmacovigilance Software tool

CLINI INDIA join hands with CREDSURE to provide secure certification for all its Programs

CLINI INDIA Celebrating International Clinical Trials Day on 20th May 2024.

In This Section

Description, program highlights, eligibility, course syllabus, key features, learning management system (lms), admission process.

• Trainer Profile
• Certification
• Placement Process

Our Placements

• Career Opportunities / Job Profiles

Salary and Career Growth

Program outcomes, cr industry.

• Student Reviews
• Hands-On Training

Welcome to the future of healthcare innovation with our Advance Program in Clinical research and management (APCRM).

Clinical Trial operations

Dive into the intricate world of clinical trials, gaining insights into protocol design, site management, and regulatory compliance. Learn to navigate the complex landscape of bringing new treatments from conception to market.

Clinical Data Management

Master the art of handling clinical data with precision and efficiency. Explore the principles of data collection, processing, and analysis, ensuring the integrity and accuracy of crucial information throughout the research process.

Pharmacovigilance

Delve into the critical domain of pharmacovigilance, where safety takes center stage. Understand the methods and systems in place for monitoring and assessing adverse drug reactions, contributing to the overall well-being of patients.

Medical Writing

Hone your communication skills to effectively convey scientific information. Learn the art of crafting clear, concise, and compliant documents essential for regulatory submissions and scientific publications.

• B.Pharm, M.Pharm and Pharm.D
• B.Sc. M.Sc and Ph.D (Biotechnology, Microbiology, Biochemistry and Nursing etc)
• B.E., B.Tech. M.Tech (Biotech/ Biomedical Engineering)
• BPT, MPT, BDS, BAMS, BHMS and MBBS etc

Clinical Trial Management

Clinical Research is the backbone of medical advancements. In the APCRM course, you’ll learn the fundamentals of clinical trials, regulations, and ethical considerations. Our curriculum includes:

Introduction to Clinical Research

Study Design and Protocol Development

Informed Consent Process

Investigator Responsibilities and Site Management

Clinical Trial Monitoring and Auditing

Data Collection, Analysis, and Reporting

Clinical Trial Safety and Risk Management

Regulatory Affairs and Compliance

Clinical Research Ethics

Adverse Drug Reaction (ADR) Reporting and Case Processing

Signal Detection and Management

Risk Assessment and Benefit-Risk Evaluation

Pharmacovigilance Database Management

Pharmacovigilance in Clinical Trials

Safety Data Exchange Agreements (SDEAs)

Pharmacovigilance Audits and Inspections

Emerging Trends in Pharmacovigilance

Introduction to Medical Writing

Regulatory Medical Writing (e.g., Clinical Study Reports)

Scientific and Research Article Writing

Investigator Brochures and Protocols

Patient Information Leaflets

Manuscript Preparation and Publication Ethics

Medical Writing for Regulatory Submissions

Medical Writing in Pharmacovigilance

Abstracts and Poster Presentations

Review and Editing Techniques

Call & Enroll over the phone with one of our representatives Ring at : +91 888.690.4030

7500+ students have upgrade their profile…

Learn From Corporate Experts / Faculty

Case Study Based Learning

Life Time Learning Management System Access

Detailed Curriculum

Mock Interviews

Flexible Batch Timings

Work on Assignments & Case Studies

Through our robust Learning Management System, students gain 24/7 access to a treasure trove of resources, including pre recorded video lecture materials, quizzes, and collaborative forums. This virtual platform facilitates seamless communication with instructors, fostering a dynamic exchange of ideas. The LMS also supports online exams via https://cliniindia.com/exam/ensuring personalized learning journeys. With user-friendly interfaces and multimedia integration, our LMS transforms education into an engaging and accessible adventure, providing the tools necessary for students to thrive in the ever-evolving landscape of clinical research and management.

Our APCRM Course Fees

Recognizing the financial challenges that may impede access to professional courses, CLINI INDIA is committed to breaking down barriers. Our APCRM course fee is thoughtfully priced at an affordable range of just 22,000/- INR only (All Inclusive). In our dedication to ensuring accessibility, we provide flexibility in payment options. Now, you have the convenience of paying for the course in two easy installments, empowering you to pursue your educational aspirations without undue financial strain. At CLINI INDIA, we believe that quality education should be within reach for everyone, and our pricing and payment structures reflect that commitment.

Candidate can easily apply through our official website. Our admission officers will review your application and contact you for further process.

Raise an enquiry via website

You will be connected to our program advisor

Select a Program and submit application form and pay registration fee

Application review and acknowledgement

Enrolment and Confirmation

Trainer Profile – Interactive Learning Environments Fees

APCRM Invites Industry faculties separate for each module. The uniqueness of our Clinical Research Course lies in its commitment to providing practical learning experiences under the guidance of domain experts. Regular workshops, case studies, and simulations orchestrated by these Full time and Visiting faculties create interactive learning environments, allowing students to bridge the gap between theory and application.

As APCRM students progress through each module, they benefit from the wealth of knowledge and practical insights offered by these dedicated faculties. The program’s success in producing industry-ready professionals is a testament to the passion and expertise that each faculty member brings to the table. With this exceptional team leading the way, APCRM continues to shape the future leaders of clinical research and management.

Certification – Clinical Research Certification

Career Triumphs: APCRM Graduates Shine Bright in Corporate Placements

Career Opportunities

Clinical Trial Management offers a diverse array of career opportunities with key roles crucial to the successful execution of clinical trials.

Clinical Research Coordinator (CRC) or Study Coordinator:

Coordinates site activities, patient recruitment, and manages trial logistics.

Clinical Research Associate (CRA):

Monitors trial sites, ensures compliance, and manages data integrity.

Clinical Trial Manager:

Oversees the entire trial process, ensuring timelines, budgets, and regulatorycompliance are met.

Clinical Project Manager:

Manages multiple trials, coordinates teams, and ensures successful project delivery.

Clinical Operations Manager:

Optimizes operational aspects, collaborating with cross-functional teams.

Clinical Quality Assurance Manager:

Ensures trials adhere to quality standards and regulatory requirements.

Clinical Trial Auditor:

Conducts audits to ensure compliance with regulations and protocols.

Clinical Trainer:

Develops and delivers training programs for clinical trial personnel.

Remote Clinical Monitoring Manager:

Manages a team of remote site monitors, ensuring effective remote monitoring strategies.

Remote Site Monitor:

Monitors patient data, documentation, and trial site activities from a remote location, optimizing trial efficiency.

These roles span pharmaceutical companies, Contract Research Organizations (CROs), academic institutions, and regulatory bodies. A career in Clinical Trial Management combines scientific rigor with project management, offering a rewarding path for professionals in the field of clinical research.

Clinical Data Coordinator:

Clinical data analyst:.

Analyzes and interprets clinical trial data, identifying trends, patterns, and potential issues.

Data Entry Operator:

Responsible for accurately entering and verifying clinical trial data into databases.

Clinical Data Manager (CDM):

Oversees the end-to-end data management process, ensuring data accuracy, completeness, and adherence to regulatory standards.

Database Programmer:

Designs and develops databases for clinical trials, ensuring efficient data storage and retrieval.

Clinical Data Quality Manager:

Ensures the quality and consistency of clinical trial data through the development and implementation of data quality plans.

Clinical Database Administrator:

Manages and maintains clinical trial databases, ensuring data security and integrity.

Clinical Data Validator:

Conducts quality checks on clinical trial data to identify and rectify discrepancies or errors.

Clinical Data Auditor:

Performs audits to ensure compliance with data management processes, protocols, and regulatory standards.

Clinical Data Scientist:

Applies advanced analytics and data science techniques to extract meaningful insights from clinical trial data.

Data Standards Manager:

Ensures adherence to data standards and establishes standard operating procedures for data management.

Clinical Coding Specialist:

Assigns standardized codes to medical terms, ensuring consistency in data representation.

Clinical Metadata Manager:

Manages metadata for clinical trial databases, ensuring accurate and standardized data definitions.

eClinical Systems Manager:

Oversees the implementation and maintenance of electronic data capture (EDC) systems for clinical trials.

Clinical Project Manager (Data Management):

Manages the data management aspects of clinical trials, coordinating with cross-functional teams.

These roles are essential for maintaining data accuracy, consistency, and compliance throughout the clinical trial lifecycle. Career paths in Clinical Data Management offer opportunities for both entry-level and experienced professionals, contributing to the overall success of clinical research studies.

Drug Safety Associate/ Case Processing Expert:

Pharmacovigilance specialist:.

Monitors and assesses adverse drug reactions (ADRs) and safety data, ensuring compliance with regulatory requirements.

Pharmacovigilance Officer:

Manages the end-to-end pharmacovigilance process, from data collection to regulatory reporting.

Clinical Safety Scientist:

Analyzes safety data, identifies trends, and contributes to risk management strategies.

Signal Detection Scientist:

Utilizes data analysis to identify potential safety signals and assess their significance.

Clinical Safety Manager:

Oversees safety aspects of clinical trials, ensuring compliance with safety reporting requirements.

Medical Reviewer:

Reviews and evaluates safety data, collaborating with healthcare professionals to ensure accurate safety assessments.

Risk Management Specialist:

Develops and implements risk management plans to minimize the potential risks associated with pharmaceutical products.

Quality Assurance Manager (Pharmacovigilance):

Ensures compliance with quality standards and regulatory requirements in pharmacovigilance activities.

Pharmacovigilance Auditor:

Conducts audits to assess compliance with pharmacovigilance processes and regulations.

Pharmacovigilance Project Manager:

Manages pharmacovigilance projects, coordinating activities and ensuring timelines are met.

Safety Database Manager:

Manages and maintains pharmacovigilance databases, ensuring accurate and timely data entry.

Medical Information Specialist:

Provides accurate and timely information on product safety to healthcare professionals and the public.

Compliance Manager (Pharmacovigilance):

Ensures adherence to regulatory requirements and internal policies in pharmacovigilance practices.

Pharmacovigilance Scientist:

Medical Writer:

Regulatory writer:, clinical research medical writer:.

Develops protocols, Informed Consent Forms (ICFs), and other clinical trial documents, facilitating the conduct of research studies.

Publication Writer:

Prepares manuscripts for publication in scientific journals, collaborating with authors to convey research findings effectively.

Scientific Writer:

Communicates complex scientific concepts to diverse audiences, creating content for educational materials, presentations, and marketing materials.

Medical Communications Specialist:

Develops materials for healthcare professionals and patients, including slide decks, training materials, and patient education materials.

CME (Continuing Medical Education) Writer:

Creates educational content for healthcare professionals to fulfill their ongoing learning requirements.

Clinical Regulatory Writer:

Prepares documents for regulatory agencies, ensuring alignment with regulatory requirements and guidelines.

Health Economics and Outcomes Research (HEOR) Writer:

Creates documents related to health economic analyses and outcomes research, contributing to market access strategies.

Medical Editor:

Reviews and edits medical documents for clarity, consistency, and adherence to style guidelines.

Pharmacovigilance Writer:

Prepares safety narratives, periodic safety reports, and other documents related to drug safety and pharmacovigilance.

Grant Writer:

Prepares applications for research funding, ensuring proposals align with funding agency requirements.

Medical Science Liaison (MSL) Writer:

Supports MSLs by creating scientific content for interactions with healthcare professionals.

Regulatory Affairs Writer:

: Prepares documents for regulatory submissions, ensuring compliance with regulatory requirements.

Freelance Medical Writer:

Works independently or on a contract basis, providing writing services to pharmaceutical companies, research institutions, and other clients.

These roles cater to individuals with strong scientific backgrounds, excellent writing skills, and a keen attention to detail. Medical writers contribute significantly to advancing scientific knowledge, regulatory compliance, and effective communication within the healthcare and pharmaceutical sectors.

The clinical research industry offers a promising career path with ample opportunities for growth, especially as professionals gain experience and expertise in specialized areas. Continuous professional development and staying abreast of industry trends can significantly enhance career prospects in this dynamic field.

The program outcomes of the Advance Program in Clinical Research and Manage’ment (APCRM) are designed to equip participants with comprehensive knowledge and practical skills in various aspects of clinical research. While specific outcomes may vary depending on the curriculum of the program, here are common program outcomes you might expect:

Understanding of Clinical Trial Operations

Ability to comprehend and apply principles related to protocol design, site management, and regulatory compliance in clinical trials.

Proficiency in Clinical Data Management

Skills in data collection, processing, and analysis, ensuring the accuracy and integrity of clinical trial data.

Expertise in Pharmacovigilance

Knowledge of pharmacovigilance principles, including adverse event monitoring, reporting, and safety assessments.

Competence in Medical Writing

Capability to prepare clear, concise, and compliant documents essential for regulatory submissions and scientific publications.

Hands-On Experience in Pharmacovigilance Database

Practical training in working with pharmacovigilance databases, providing real-world experience in the tools and technologies used in the industry.

Critical Thinking and Problem-Solving Skills

Development of analytical skills to assess and address challenges encountered in clinical research settings.

Effective Communication

Enhanced communication skills for conveying scientific information to diverse audiences, including healthcare professionals and regulatory bodies.

Adherence to Ethical Standards

Emphasis on ethical considerations in clinical research, including participant rights, confidentiality, and regulatory compliance.

Project Management Skills

Understanding the principles of project management to effectively plan, execute, and monitor clinical research projects.

The Top Sectors within the Clinical Research Industry

Pharmaceutical Companies

Conduct clinical trials to test the safety and efficacy of new drugs and bring them to market.

Contract Research Organizations (CROs)

Provide outsourced services to pharmaceutical companies, managing various aspects of clinical trials, including site selection, data management, and monitoring.

Biotech Companies

Engage in research and development of biopharmaceutical products, conducting clinical trials to assess their safety and effectiveness.

Academic and Research Institutions:

Conduct clinical research to advance scientific knowledge, often collaborating with pharmaceutical companies and other organizations.

Government Health Agencies

Oversee and fund clinical trials to assess the safety and efficacy of new treatments or interventions.

Medical Device Companies

Conduct clinical trials to evaluate the safety and performance of medical devices before regulatory approval.

Clinical Research Sites and Hospitals

Serve as locations where clinical trials are conducted, providing patient care and data collection.

Regulatory Affairs Agencies

Assist in navigating regulatory requirements, ensuring compliance with laws and regulations.

Data Management and Statistical Analysis Firms

Provide services related to data management, statistical analysis, and interpretation of clinical trial data.

Pharmacovigilance and Drug Safety

Monitor and assess the safety of drugs post-approval, managing adverse event reporting and ensuring compliance with safety regulations.

Site Management Organizations (SMOs)

Specialize in the management of clinical trial sites, ensuring efficient conduct and compliance.

Clinical Trial Supply and Logistics:

Manage the logistics of clinical trial supplies, ensuring proper distribution and storage of investigational products.

Medical Writing and Communication

Prepare regulatory documents, clinical study reports, and other written materials essential for communication within the industry and with regulatory agencies.

Quality Assurance and Compliance

Ensure adherence to quality standards, regulatory requirements, and ethical guidelines in clinical research activities.

Health Economics and Outcomes Research (HEOR)

Assess the economic impact and outcomes of healthcare interventions, providing data to inform healthcare decision-making.

These sectors collectively contribute to the advancement of medical knowledge, the development of new therapies, and the improvement of patient care. Professionals in the Clinical Research Industry may find opportunities in one or more of these sectors based on their skills, interests, and career goals.

Testimonials

What our students have to say.

Listen to the stories of our students, as they articulate the profound influence of our educational environment. Their testimonials encapsulate the enriching experiences and valuable insights gained throughout their educational endeavors.

Doing the CR program from CLINI INDIA was a life-changing experience for me. The practical skills backed by academic knowledge have given me the confidence to pursue a career in any domain in the Clinical Research Industry.

The quality of lecturers surpassed my expectations, and they represented a great blend of all modules in Clinical Research. I found the program is a milestone in my professional career.

My Training at CLINI INDIA was full of learning with the utmost knowledge. It made many positive frameworks in my attitude, Technical skills, work style, personality and behavior to shape best out of this Competitive world or Clinical Research. Thanks to Team CLINI INDIA for career support.

Anurag Shukla

Enrolling in CLINI INDIA was a valuable investment for me. In addition to broadening my perspective in the Clinical Research field, it has helped me to grow both professionally and personally. Thanks to CLINI INDIA, I am working with World’s Leading CRO in Bangalore

Prasanta Kumar Gouda

CLINI INDIA is a great institution. The staff and instructors are always helpful and are looking out for you. I have got placement before my course Completed. The atmosphere is great. I have made friends that I will have forever.

Golak Bihari Praharaj

Hands-on training in pharmacovigilance database.

Our program goes beyond theory by providing practical, real-world experience. You’ll have the opportunity to engage with pharmacovigilance databases, gaining hands-on proficiency in the tools and technologies used in the industry. This immersive experience will enhance your confidence and readiness to tackle challenges in the field.

Why Choose APCRM?

Comprehensive Curriculum

Covering key aspects of clinical research, our program ensures you are well-versed in every facet, setting you on a path for success. Read Full

Industry-Driven

Flexible Online Learning

Embark on a transformative journey with APCRM, where we nurture the next generation of clinical research leaders.Join us in shaping the future of healthcare through excellence in research and management.

Here Is The Most Frequently Asked Questions

What is clinical research, and why is it important for healthcare, how can i start a career in clinical research as a fresh graduate, what skills are essential for a career in clinical research, are there specific educational requirements for entering the field of clinical research, what types of job roles are available in clinical research for entry-level professionals, how important is networking in building a career in clinical research, what are the key challenges faced by professionals in clinical research, can i get 100% placement guarantee after completion of the program, what role does ethical considerations play in clinical research, and how are they addressed, what are the potential career advancement opportunities in clinical research.

DISCLAIMER: Placement Services

CLINI INDIA would like to bring to the attention of its students and stakeholders that our institute does not provide any placement services or guarantee job placements in any form. While we strive to offer quality education and skill development, securing employment remains the responsibility of the individual student.

We encourage our students to actively participate in career development activities, utilize the resources provided by the institute, and take advantage of networking opportunities to enhance their employability. [Institute Name] may facilitate career-related workshops, seminars, or connect students with industry professionals, but this is solely for educational and informational purposes.

It is essential for students to exercise due diligence, proactively seek employment opportunities, and engage with potential employers independently. Any claims or representations suggesting guaranteed placements by external entities or individuals on behalf of CLINI INDIA are not endorsed by the institute.

This disclaimer serves as a notice to all students, alumni, and stakeholders regarding our institute’s policy on placements. For any clarification or inquiries, please contact the institute’s administration.

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Bangalore ICRI

ICRI, Bangalore

ICRI, Bangalore , established in 2004 is one of the 9 campuses of ICRI India. With world-class infrastructure and a team of highly experienced faculty. Since its establishment, ICRI has constantly been growing with the aim of achieving the best-in-class education system for students in specialized areas. ICRI Bangalore Campus offers a wide range of courses in Clinical Research, Aviation, Logistics & Supply Chain Management. The institute offers B.Sc., M.Sc., Diploma and PG Diploma at the UG and PG level. Admission to the courses offered will be done based on the candidate’s performance in entrance examination. ICRI aims at providing a 100% placement assistance to its students.

Table of Content

ICRI Bangalore Key Facts

Icri bangalore awards, icri bangalore courses.

• ICRI Bangalore Admission
• ICRI Bangalore Placement

ICRI Bangalore FAQs

• Opportunity to study in a real-time hospital environment
• Successful candidates can get an internship with our Hospital Network which may lead to further job opportunities.
• first-hand experience of working and observing how clinical trials are conducted.
• Prominent clinical trial investigators offer training to help you succeed in your research.
• Some of the top recruiters of ICRI India, are Fortis, Excel life Sciences, PACRA, Max Neeman International, BioXcel, and Wipro.
• The institute has a well-equipped library with a wide range of books and journals on Clinical Research.
• Best Institution in New Age Careers - Prestigious Brand in Education Economic Times- 2021
• Best Institution in Aviation & Logistics Saksham Education Award- 2020
• Best Institution in Clinical Research & Healthcare Indian Eduaction Award by Economic Times- 2019
• Best Institution in Clinical Research & Healthcare Indian Eduaction Award by Economic Times 2018
• Best Institution in Clinical Research & Healthcare Management- Careers of Tomorrow Economic Times - Making of Developed India - Excellence in Healthcare- 2018

ICRI offers B.Sc, M.Sc, Diploma and PG Diploma courses at the UG and PG level. The details of the courses offered are given below: 

Check: ICRI Bangalore Courses & Fees

ICRI Bangalore Admission 

The mode of application at ICRI Bangalore is online. The steps involved in the admission process is given below: To apply for admission, the candidates must follow the given steps-

• Visit the official website of the institute.
• Click on “Apply Now”
• Fill in the mandatory details to successfully register.
• Login using the credentials.
• Fill in the application form- Personal details, Academic qualifications
• Upload the necessary documents
• Pay the requisite fee of INR. 1300/-
• Submit the form
• The application fee can be paid online via debit/credit card or offline via demand draft in favor of ICRI Bengaluru.
• The candidates must take a print out of the completed application form for future reference.

Check: ICRI Bangalore Admission

ICRI Bangalore Placement 

ICRI ensures 100% full placements as it has tie-ups with around 500 companies. In addition to this, there are also ICRI Internship programmes offered to students.

Top recruiting companies include:

Wipro, TCS, Accenture, Ranbaxy, HCL and many more.

Ques. Why should I choose ICRI?

Ans. One should opt for ICRI because of the following reasons:

• ICRI has more than 2000+ industry partners.
• 12000+ Alumni Network Globally.
• ICRI has taken initiative partnering for various training and research programs with organizations like AHA, DIA, UKIERI.
• The university was the first which launched the first book on Clinical Research and Pharmacovigilance.
• 90% of ICRI Trainees get absorbed by companies for permanent positions

Ques. How much is the total fees of M.Sc in ICRI?

Ans. The total fees is of INR 2.50 Lacs for pursuing M.Sc from ICRI Bangalore

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There are many areas of research to choose from. After which the student has to develop a synopsis and a thesis to work on for three years. The thesis requires dedication by the student in developing and presenting it to the committee for approval.

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Shifali Vohra's Review On ICRI, Bangalore

The three year course is divided into six semesters. It involves the fundamentals of Clinical Research and Pharmacology. It also teaches healthcare management and quality assessment along with fieldwork and practical experience.

Nice college offering good variety of courses

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If one has given any national or state level entrance examination for admission to the BBA program then it is not required to give the entrance exam conducted by the college.

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Advanced Diploma in Clinical Research- ADCR

ONLINE | CLASSROOM | CAMPUS TRAINING | FREE WEBINARS

Our training centre offers an affordable Diploma program in Clinical Research, equipping students with the latest knowledge and effective teaching methods to prepare them for successful careers. Join us today to reach your fullest potential.

BCRI provides you an innovative learning approach which allows you as a student to apply the theoretical knowledge and skills gained during the taught Clinical Research Courses in an effective manner in the clinical research industry.

Kick start your career in a CRO

Advance your career with BCRI’s job-oriented Clinical Research Course. Get personalized guidance and hands-on experience from industry experts to succeed in the exciting field of clinical research. Enroll now to unlock your potential!

Our Advanced Diploma in Clinical Research Course helps healthcare professionals achieve their full potential in just four months. You’ll learn about important topics like Clinical Research, Clinical Data Management , Pharmacovigilance and intermediate regulatory affairs to help you succeed in your career advancement.

Our tutors are experienced professionals and will give you practical knowledge that you can use to make a difference in your career. You’ll earn an Advanced Diploma in Clinical Course and gain important tools for professional growth.

Why Advanced Diploma in Clinical Research Course ?

The Advanced Diploma in Clinical Research is a program designed in such a way by the Bangalore Clinical Research Institute (BCRI) that it helps aspiring candidates learn about all important aspects of clinical research. The Advanced Diploma in Clinical Research course curriculum equips candidates with the right skills required to pursue careers in the clinical world.

This programme is built to produce high-quality clinical research professionals with the correct skill set needed to work in CROs. The Advanced Diploma in Clinical Research course opens a wide array of career options for candidates.

Skills you gain with (ADCR) - Clinical Research Diploma

• Phases of clinical trials
• Conduction of Clinical Studies
• Trial design
• Active control studies
• Clinical Data Management
• Data management plan
• Regulatory Affairs
• FDA Good Clinical Practice (GCP)
• ICH Good Clinical Practice (ICH-GCP) guidelines clinical trials
• GMP and other good practices

CDM systems

Study Set-up

Creating standards

Clinical Trial Management

Study Conduct

• Pharamacovigilance
• Safety signals
• Quality System In PV

PV Database Index

• Causality assessment
• Narrative Writing

Who can Join ADCR?

The Advanced Diploma in Clinical Research is a four-month course. Anyone with a minimum 55% score in graduation in any of the life sciences or medical sciences can join this course, like MBBS, BDS, etc.) or a degree in science, pharmacology, pharmacy, life sciences, biotechnology, biochemistry, etc., pursued from a recognised university.

Admission to the Advanced Diploma in Clinical Research course depends on a candidate’s overall merit or performance in the relevant entrance examination conducted by the Bangalore Clinical Research Institute (BCRI).

• How many phases of clinical studies are there
• A phase 0 study and Phase 5 clinical trial
• Difference between clinical trial and clinical research
• Clinical Research vs. Medical Care
• What Is a Clinical Study?
• Clinical Trials
• Observational Studies
• Site for Clinical Studies and duration and Reasons for Conducting Clinical Studies
• Participating in Clinical Studies and Who Can Participate in a Clinical Study?
• Participants Protection and Considerations for Participation
• Relationship to Usual Health Care
• Phases of FDA approval
• Percentage of drugs fail clinical trials
• Microdosing
• Dose Ranging
• Single ascending dose (Phase Ia)
• Multiple ascending dose (Phase Ib)
• Efficacy vs Effectiveness
• Investigational new drug and New drug application

Process flow

• Study set up
• Tracking CRF Data
• Entering data
• Managing lab data
• Identifying and Managing discrepancies
• Collecting adverse Event Data
• Where systems come from?
• Choosing vendor products
• Implementing New Systems
• System Validation
• Migrating legacy Data
• Change control
• Approved Protocol
• Project Plan
• eCRF Specification
• Visit Form Matrix
• IxRS Integration
• Final Sign off – Go Live
• Creating hierarchies
• Sops and guidelines
• Working with CROS
• CRF Design Consideration
• Remote Data Entry
• Data entry in RDC and Discrepancy Management in RDC
• Auto coder Algorithms
• Fundamentals of clinical trials
• Basic statistics for clinical trials
• Clinical trials in practice
• Reporting and reviewing clinical trials
• Protocol development
• Trial designs
• Project management and research co-ordination
• Regulatory affairs, good clinical practice and ethics
• Data management
• Data monitoring and interim analyses
• Data reconciliation
• DCMs and DCIs
• Tracking CRF
• Data Creating, Data Collection Modules and layouts
• corresponding to CRFs to allow for data entry
• Entering data, Generating and Testing data entry screens and validate the range,
• format, date, missing fields
• Data validation
• User acceptance testing (UAT)
• Collecting AE Data
• SAE Reconciliation
• Reviewing clinical data as per SOP, protocol, and study specific guidelines
• Medical Coding
• IxRS Reconciliation
• Listing Reviews, consistency checks
• Status Reports
• All Subjects completed final visits/f-up visits
• Medical Coding data review completed and issues resolved
• Final SAE reconciliation
• All queries resolved and DB updated
• Final review completed
• All expected forms and visits are locked/frozen
• QC steps conducted and QC plan and report documented
• QA issues addressed if any
• All documentation completed as per DMP and stored according to SOP
• Data is archived/submitted

Introduction of Drug Discovery and Development

• Discovery and Development
• Preclinical Research
• Clinical Research
• Drug Review
• Post Market Drug Safety Monitoring

Introduction to Pharmacovigilance

• Pharmacovigilance (WHO Definition)
• History of Pharmacovigilance
• Scope and purposes of Pharmacovigilance
• Basic Concepts: Terms and definitions
• General idea of PV and types of AE reporting
• Types and sources of data
• The process of Pharmacovigilance- Signal Detection and Drug recall
• What are safety signals?

  Pharmacovigilance Reporting Database

•   Risk Assessments & Evaluation
• Reporting Criteria to Health authorities and timelines
• Expedited Reporting Criteria
• PSUR & PBRER
• Different reporting formats used in PV
• PSUR and DSUR overview
• PV Database and Signal Detection
• Safety ignals
• Signal Management
• Risk Assessments & Managements
• Case receipt
• Data verification and validity check
• Duplicate search
• Book in and registration
• Coding of AE and Drugs

  Causality assessment

• Expectedness assessment
• Why causality assessment
• WHO –UMC causality assessment system
• Case Narrative
• Quality check
• Reporting or Submission
• Deletion and nullification
• Initial Receipt date and Day 0 Importance
• Case linking, Mother and Baby cases
• Special Case Scenarios: LOE, Off-Label use, Misuse, Overdose, Pregnancy &
• Medication Error
• Practicing Real Time cases scenarios

Drug Dictionaries, ADR dictionaries and Coding of the events

• WHO drug dictionary
• ADR classification
• SAE and Seriousness criteria

  Narrative Writing

•   Overview and Characteristics Case Narrative
• Sections of Case Narrative
• Steps and Construction of a narrative
• Introduction to Global Regulatory Authorities for pharma and healthcare industries
• Regulatory affairs in clinical research
• WHO –UMC (Uppsala Monitoring Committee), CIOMS
• Drug Development Process, Clinical Trials and related norms and regulations
• European Pharmacovigilance System
• International Council for Harmonisation
• GCP in pharma, Main GCP principles, GCP compliance
• GMP and other good practices.
• Institutional review board (IRB) / independent ethics committee (IEC)
• Quality Assurance and Drug Regulations, ICH and WHO guidelines
• Technical Requirements for Pharmaceuticals for Human Use
• Data monitoring committees
• European Forum for Good Clinical Practice (EFGCP), European Medicines Agency  (EMEA)
• Dossier preparation in CTD format, eCTD submissions
• Healthcare Industry IPR, Patents, copyrights and Trademarks
• Pharma and Healthcare products- Marketing, Import and Export regulations
• Compliance guidelines, Govt. Audits (FDA, MHRA, PMDA, TGA, DCG, etc) and Breach reports
• Indian GMP Regulations

The Advanced Diploma in Clinical Research (ADCR) program equips students with a diverse set of skills essential for a successful career in the clinical research field. You’ll develop a solid understanding of the principles, regulations, and processes involved in clinical research. This includes practical knowledge, EDC software, Case processing, Narrative writing, etc..

The coverage of pharmacovigilance and drug safety monitoring in an Advanced Diploma program typically involves a comprehensive exploration of the intricacies of monitoring and ensuring the safety of pharmaceutical products throughout their lifecycle. The Advanced Diploma program covers Pharmacovigilance Overview, Drug Safety Monitoring, Regulatory Aspects, Expedited and Periodic Safety Reporting, and Hands-On Experience.

The role of practical training or internship in an Advanced Diploma in Clinical Research is crucial for several reasons, and it significantly enhances the overall learning experience of participants. Practical training and internships are integral components of the Advanced Diploma in Clinical Research. Practical training allows participants to apply theoretical knowledge in real-world scenarios. It bridges the gap between classroom learning and the actual practices within the clinical research industry. Participants have the opportunity to develop and hone practical skills essential for roles in clinical research, such as data collection, monitoring, regulatory compliance, and project management with EDC software like Clinevo .

BCRI’s Advanced Diploma program prepares students for roles in clinical research by providing specialized coursework and practical training, emphasizing in-depth knowledge of trial design, data management, and regulatory affairs. The program aims to equip students with a comprehensive skill set for leadership positions in the industry.

The Advanced Diploma in Clinical Research program covers essential topics to equip healthcare professionals for successful careers in the clinical research field. The key modules you’ll explore during this course are Clinical Research, Clinical Data Management, Pharmacovigilance, Regulatory Affairs, and developing skills in writing clinical trial protocols, reports, and other scientific documents. This comprehensive program aims to prepare you for a rewarding career in the clinical research industry. If you have a background in life sciences or medical sciences, you’re eligible to join this four-month course and unlock your potential!

The ADCR course duration is four months. The course is conducted live instructor mode. Everyday sessions would be for 1 to 1.5-hour, followed by hands-on assignments and class recordings.

Anyone who is Life science, Pharmacy, Medical Graduates & Post Graduates (including BDS, BAMS, BHMS, BPT) are eligible for Advanced Diploma in Clinical Research Course.

Absolutely! Our training materials and courses are designed for easy access, our courses are structured into independent modules like a) Pharmacovigilance b)Regulatory affairs c)Clinical Research d)Clinical Data Management with distinct learning procedures and practical applications on real-time scenarios.

The Trainers at BCRI India are well organized and experienced in their fields like clinical Trial Management, Clinical Data Management, or Regulatory Affairs. The trainers will take responsibility for evaluating the needs and current practices and creating a development plan with materials and learning resources.

Our Trainers are confident public speaker and subject Matter specialist to educate. Our Trainers are up-to-date on the latest tools and Industry resources needed to improve employee training and performance.

The BCRI Clinical Research trainer will also be responsible for researching and selecting the best platform to deliver and utilize training materials. Bangalore Clinical Research trainers can design and implement various learning and developmental programs for clinical research for comfortable working in the industry with groups of all sizes. Our trainers are experienced, dynamic, well versed in strong clinical industry knowledge with excellent communication, management, and developmental skills.

BCRI trainers have not only the ability to convey information concisely and accurately but also the ability to make the students highly potential and competitive by providing real-time exercises.

Yes, We do have 100% placement Support on the successful completion of the course. Each student is entitled to placement assistance. Our placement officer is dedicated to finding a suitable opportunity for each student.

We are proud to state within a short duration, we have been successful in placing our students in the field of clinical operations as CRCs and process coordinators, as drug safety associates in Pharmacovigilance departments, QA personnel in medical writing departments, and as Jr. SAS programmers.

Students who have completed a course in clinical research from any other organization may approach us for internship assistance. We cannot guarantee that a company will hire you, as it is based on your performance during an interview. However, we do provide 100% placement assistance. To date, we have a 100% Placement record.

Online Advanced Diploma in Clinical research course is conducted using an online training platform like Zoom.us, goto training, google meet, etc. Online clinical research is a good way of learning from any part of the world.

As compared to conventional classes opting for online ADCR classes are a better choice to learn clinical Research, Clinical Data Management, Pharmacovigilance, and Regulatory Affairs. During online classes, you get everyday class recordings for lifetime access along with e-notes and assignments.

BCRI distinguishes itself in clinical research training through a comprehensive curriculum, hands-on projects, and potential industry collaborations, fostering advanced skills for successful careers. For specific details, consult BCRI’s promotional materials or contact the institution directly.

To enroll in our Advanced Diploma in Clinical Research (ADCR) program, please visit our official BCRI website, where you’ll find the admissions section. Follow the provided application process and submit the necessary documents. If you have any questions or need guidance, feel free to contact our admissions department. We look forward to welcoming you to BCRI.

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Bangalore Clinical Research Institute

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Best Clinical Research Training Courses in Bangalore as on Aug 30, 2024

Clinilaunch research institute llp.

Clinilaunch Research Institute LLP, situated in Bangalore's Koramangala, is a renowned institution specializing in clinical research education and training. With a focus on industry-relevant curriculum and practical skill development, Clinilaunch prepares students for rewarding careers in the fast-growing field of clinical research. The institute offers comprehensive courses covering various aspects of clinical trials, regulatory affairs, and data management, equipping students with the knowledge and expertise needed to excel in diverse roles within the pharmaceutical and healthcare sectors. Through hands-on training, industry interactions, and internship opportunities, Clinilaunch ensures that students gain real-world experience and insights into the complexities of clinical research. With a track record of academic excellence and industry placements, Clinilaunch Research Institute LLP is a preferred destination for aspiring clinical research professionals.

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" Communication 5/5 responsiveness 5/5 good price 5/5 ontime services 5/5 Service Quality 5/5"

Sprychampion Institute

"i am so grateful for trainers who radiates positivity and values personal intuition. teaching is very smooth. her class helped me alot of to ramp up with java/selenium skills. and in finally i got placed in a good company through this institute."

"I completed the software testing in this center.very satisified about the course.this is the good center to learn clearly with quality.staffs are also very kind and teaching very good.I preferred this center for good learning..."

Hemant Sound Studio

"Best place to find out dream job here"

HR Courses in Bangalore

International centre for culinary arts dubai .

"When I visited the icca institute it had been great! I ought to meet a number of my professors that I might have and met with tons of the admissions office. Everyone was friendly and helpful and took the time to answer questions. The institute ambience is extremely good. The best college for learning Cooking. One can go into the hotel field and may achieve their dreams to become an excellent chef. the school has good records of placement. it's been an honest experience thus far. the school are very experienced from the industry and teaching. there's an honest industry exposure and therefore the placements also are good."

"I enrolled in the culinary courses here and I loved it! The teachers are very professional and I learnt a lot from them and it is very useful for me. Explained everything well, answered our questions and helped our technique while we cooked course. If you're looking to get a career change and be fully equipped with the right tools and right contacts. In Icca Dubai gave me wings to explore the world of food. it was a wonderful experience doing professional chef course here. "

Mozavi Technologies Pvt. Ltd.

Indian healthcare bpo, apex medcom.

"My friend Enrolled in this Apex Medcom Domlur, Bangalore. In this institute, he has joined for Medical Billing. The way of response to their explanations of the course was very nice he paid Rs 19,000 including Exam fees and Book materials. The course duration was 3 months weekly 4 classes Monday to Thursday hour they taking 3 to 4 hrs The institute atmosphere and coaching was good"

"Happy to share my experience with this institute, Health & wellness training (Medical Billing) purpose I have joined this institute, they gave the best response. they charged me 15000 for the course fees, the course duration was 2 months its daily classes Monday to Thursday. The experienced faculty is training us. giving me good knowledge about the course. this institute has a good learning environment. I'm glad to join in this institute."

Leads Clinical Research Pvt. Ltd.

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