Exclusive at BCRI ✦ Hands-On Clinical Data Management & Pharmacovigilance Training with Database Access ✦ Unavailable Elsewhere!

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PG Diploma in Clinical Research with CRA/CRC

Get job-ready with BCRI’s 5.5-month live online training in Clinical Research, CDM, Pharmacovigilance, and CRA/CRC roles.

Fees: ₹57,000 | Optional Internship: SMOs & Hospitals in Bangalore

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Committed To Clinical Research Training Excellence

We prepare students for real-world roles in global clinical research by delivering up-to-date PGDCR and CRA/CRC-focused training, live mentoring, and hands-on exposure through SMO and hospital-based internships.

Take the next step in your clinical research career with BCRI’s 5.5-month online PG Diploma in Clinical Research with CRA/CRC. This program covers Clinical Research, Clinical Data Management, Pharmacovigilance, and CRA/CRC Modules — preparing you for critical on-site roles such as CRCs or entry-level CRAs at SMOs, hospitals, CROs, and pharma companies.

PG Diploma in Clinical Research with CRA/CRC

A 5.5-month live online training program covering Clinical Research, Data Management, Pharmacovigilance, and practical CRA/CRC operations — designed for non-programmers seeking real clinical site roles. Optional internships included.

The PG Diploma in Clinical Research with CRA/CRC by BCRI is a career-focused training program crafted for graduates in Life Sciences, Pharmacy, Medicine, Nursing, and related fields. If you’re aiming to build a strong career in clinical research — but prefer patient-facing or documentation-based roles instead of programming, this course is the perfect fit.

You’ll gain real-world knowledge of clinical trial processes, site management, source documentation, protocol compliance, subject handling, and trial monitoring — all aligned with global standards like ICH-GCP, Schedule Y, FDA, EMA and Indian regulations.

This hands-on course goes beyond theory with live instructor-led sessions, practical assignments, role-play exercises, regulatory form filling, and mock interviews — helping you confidently apply for entry-level roles such as Clinical Research Coordinator (CRC), Clinical Research Associate (CRA), or Site Monitor.

Students also have access to optional internship opportunities at SMOs and hospitals in Bangalore, enhancing job readiness through real trial exposure. After completing this course, you’ll be equipped to start a rewarding career in Clinical Operations, Data Management, Pharmacovigilance, and site-based roles — in India and internationally.

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Join a job-orientated PG Diploma in Clinical Research with CRA/CRC training at BCRI, with an excellent placement track record.

📘 What You Will Learn in BCRI’s PG Diploma in Clinical Research with CRA/CRC

This 5.5-month job-oriented training equips students across four core domains—Clinical Research, Clinical Data Management, Pharmacovigilance, and CRA/CRC operations—making them eligible for diverse site-based and clinical operations roles.

🧪
Clinical Research (CR)
Explore clinical trial phases, drug development lifecycle, ethical guidelines, and trial monitoring processes aligned with ICH-GCP, FDA & Schedule Y standards.
📊
Clinical Data Management (CDM)
Gain practical training in CRF design, discrepancy management, query handling, EDC tools (Clinevo), medical coding, SAE reconciliation, and CDM workflow.
🩺
Pharmacovigilance (PV)
Understand AE/SAE reporting, MedDRA coding, signal detection, case narrative writing, and aggregate safety reporting (PSUR, DSUR, PBRER) using Clinevo database.
👩‍⚕️
CRA/CRC Operations
Learn site coordination, informed consent process, source documentation, recruitment strategies, trial monitoring, and regulatory submissions at the site level.
🎯
Internship & Placement Support
Optional internship opportunities at SMOs and hospitals in Bangalore. Resume building, interview prep, and guidance from industry mentors.
🚀
Launch Your Clinical Research Career
Ready to become a CRC or CRA? Enroll now in BCRI’s PG Diploma with CRA/CRC Program and step confidently into a career in global clinical research.

🎯 Learning Objectives of PG Diploma in Clinical Research with CRA/CRC

  • Understand the entire Clinical Research lifecycle and regulatory framework (ICH-GCP, Schedule Y, FDA/EMA).
  • Gain exposure to Clinical Data Management activities including CRF design, data cleaning & coding using Clinevo database.
  • Learn Pharmacovigilance processes such as AE/SAE reporting, MedDRA coding, and case processing using Clinevo Safety DB.
  • Master CRA/CRC responsibilities including site monitoring, source documentation, informed consent, and visit coordination.
  • Prepare for real-world roles through practical assignments, mock interviews, resume guidance, and optional internships.

📘 Course Modules – PG Diploma in Clinical Research with CRA/CRC

The program includes in-depth modules across Clinical Research, CDM, PV, Regulatory Affairs, CRA/CRC Operations, and hands-on tools like Clinevo EDC.

📌 Clinical Research
  • Overview of Clinical Research & Trial Phases
  • Phase 0 to Phase 5 Studies
  • Trial Designs: Efficacy vs. Effectiveness
  • IND, NDA, SOPs, and Working with CROs
  • Participants, Ethics, and Regulations
📌 Clinical Data Management
  • Data Management Plan (DMP)
  • Study Setup, CRF Design, DB Development
  • eCRF, DVS, UAT, IxRS, and Go-Live Activities
  • EDC Tool: Clinevo Hands-on
  • Discrepancy Management, Validation & QC
📌 Pharmacovigilance
  • Introduction to PV, AE/SAE Classification
  • Case Processing: Receipt to Submission
  • MedDRA Coding, WHO-DD, Causality & Expectedness
  • Aggregate Reports: PSUR, DSUR, PBRER, PADERS
  • PV Tool: Clinevo Safety Database Hands-on
📌 Regulatory Affairs
  • Global Regulatory Authorities: FDA, EMA, DCGI, WHO
  • CTAs, Schedule Y, ICH-GCP, Ethics Committees
  • Protocol Design, Investigator Brochure, IC
  • Indian GMP, GLP, QA, IRB/IEC
📌 CRA / CRC Operations
  • Roles & Responsibilities of CRC & CRA
  • Site Initiation, Monitoring & Close-out Visits
  • IRB/IEC Coordination & Essential Documents
  • Source Documents, Patient Recruitment
  • Clinical Trial Process in India
📌 Optional Internship (Bangalore)
  • On-site Internship at SMOs/Hospitals
  • Real-time Trial Documentation (CRF, ISF, TMF)
  • Clinical Trial Monitoring Practice
  • Mock Interviews & Resume Building
  • Mentorship from Senior CRCs/CRAs

✅ Key Highlights of the PG Diploma in Clinical Research with CRA/CRC

🎓 Comprehensive 5.5-Month Online Program

Includes Clinical Research, CDM, Pharmacovigilance, Regulatory Affairs & CRA/CRC modules in a career-aligned format.

👨‍🏫 Live Classes by Industry Experts

Learn directly from senior professionals with 10–15+ years of experience in clinical operations and site coordination.

🏥 Optional Internship in Bangalore

Gain real-world exposure through internships at SMOs and hospitals, with trial document handling and CRC practice.

🗂️ Job-Oriented CRA/CRC Training

Practical focus on site-based operations, ICH-GCP, ethics submissions, source documentation, and subject management.

📚 LMS Access + 4-Month Session Recordings

Access recorded classes and training materials anytime via BCRI’s Android, iOS & Windows learning apps.

💼 100% Placement Support

Interview training, resume building, mock interviews, and placement assistance with CROs, hospitals & pharma firms.

🌐 Global Regulatory Readiness

Curriculum aligned with FDA, EMA, ICH-GCP & Schedule Y guidelines — relevant to clinical job markets worldwide.

🚀 Career Flexibility in Clinical Domain

Become eligible for roles in CRA/CRC, Trial Documentation, PV, CDM & Clinical Operations in India & abroad.

PG Diploma in Clinical Research - Course Fees

Flexible Learning, Career-Focused Training

PG Diploma in Clinical Research

( PGDCR with CRA, CRC )
  • Mode (Online/Classroom)
  • Live interactive classes
  • Industry-expert trainers
  • Real-World Case Studies
  • Training with Live Databases
  • Live class recoding Access

📋 Course Details – PG Diploma in Clinical Research with CRA/CRC

FeatureDetails
Course NamePG Diploma in Clinical Research with CRA/CRC
Duration5.5 Months (Live Online Classes)
Mode of DeliveryLive Instructor-Led Online Sessions (Includes recordings, notes, and LMS access)
Focus AreaClinical Research, Clinical Data Management, Pharmacovigilance, and CRA/CRC Operations
Key Topics CoveredICH-GCP, Schedule Y, Site Monitoring, Source Documentation, AE/SAE Reporting, eCRF, Regulatory Submissions
Tools/Formats UsedClinion, Clinevo, MedDRA, WHO-DDE, Informed Consent Forms, Investigator Site File (ISF)
EligibilityB.Pharm, M.Pharm, B.Sc, M.Sc (Life Sciences), MBBS, BDS, BHMS, BAMS, or working professionals in healthcare
AssessmentAssignment-based evaluation + Mock tests + Final Assessment + Project-based evaluation
CertificateBCRI PG Diploma Certificate (with specialization in CRA/CRC)
Placement Support100% Placement Assistance – Resume Building, Mock Interviews, Interview Referrals, Internship with SMOs/CROs/Hospitals

🎯 Career Opportunities After PGDCR with CRA/CRC

💼 Job Roles You’re Eligible For

  • Clinical Research Coordinator (CRC)
  • Clinical Research Associate (CRA)
  • Clinical Trial Assistant (CTA)
  • Drug Safety Associate
  • Pharmacovigilance Officer
  • Clinical Data Coordinator
  • Clinical Operations Executive
  • Regulatory Affairs Associate

🏢 Companies That Hire

  • Contract Research Organizations (CROs)
  • Pharmaceutical & Biotech Companies
  • Hospitals & Multispecialty Clinics
  • Site Management Organizations (SMOs)
  • Healthcare BPOs & Clinical Trial Units
  • Regulatory Consulting Firms

🌍 Global Work Opportunities

  • Bangalore, Hyderabad, Mumbai, Pune, Chennai, Delhi NCR
  • On-site roles in SMOs, Hospitals, and CROs
  • Remote jobs with global CROs and pharma KPOs
  • Opportunities in the USA, Canada, UK, Europe & Middle East
  • Growing demand in APAC clinical trial hubs
💼 Global Salary Trends for PGDCR with Clinical SAS Graduates

Graduates of BCRI’s PG Diploma in Clinical Research with CRA/CRC are eligible for diverse site- and sponsor-based roles globally. The salary figures below are based on authentic sources like Payscale, AmbitionBox, Glassdoor, and official labor statistics.

🌍 Country-wise Average Salary (Clinical Research Associate)

CountryAverage Annual Salary
🇮🇳 India₹9.27 lakh (≈ $11,200)
🇺🇸 USA$98,000 (range $76k–$110k)
🇨🇦 CanadaCAD 95,100 (≈ $72,000 USD)
🇬🇧 UK£30k–£43k
🇦🇺 AustraliaAUD 75k–110k (~$50k–$75k USD)

💼 Salary Trends in Clinical Research, CDM, PV, CRA & SAS

Salaries in the Clinical Research domain vary based on geography, job role, and experience. Below are indicative salary ranges across India, USA, and Canada.

Job RoleIndia (₹/Year)USA ($/Year)Canada (C$/Year)
Clinical Data Manager₹5–8 LPA$85,000–115,000C$70,000–90,000
Pharmacovigilance Associate₹4.5–7.5 LPA$75,000–100,000C$65,000–85,000
Clinical SAS Programmer₹6–10 LPA$90,000–125,000C$75,000–95,000
Clinical Research Associate₹4.5–8.5 LPA$70,000–110,000C$65,000–90,000
India Salary Trends Global Salary Trends
Invest in Your Future - Enroll Now!

Take the next step in your career with our industry-recognized PG Diploma in Clinical Research with CRA – CRC. Secure your spot today!

FAQs About PGCR

The eligibility criteria for the Post Graduate Diploma in Clinical Research (PGDCR) program are that the Candidates should have completed their graduation degree in any of the following fields: a) Science (e.g., Biochemistry, Microbiology, Genetics, Biotechnology, Botany, Zoology) b) Medicine (e.g., MBBS, BDS, BPT, BAMS, BHMS, BUMS) c) Pharmacy or Pharmaceutical Sciences(e.g B.Pharm, Pharm.D).

After completing a PG Diploma in Clinical Research, graduates can work in various roles such as Clinical Research Associate, Clinical Data Manager, Biostatistician, Clinical SAS Programmer, Pharmacovigilance Specialist, and many more in pharmaceutical and healthcare companies.

Our 7.5-month program PG diploma in clinical research covers major domains like Clinical Research, Clinical Data Management, Pharmacovigilance, Regulatory Affairs, and Clinical SAS. Students benefit from practical, hands-on training and gain expertise in using EDC software like Clinevo and Saftey Database—a valuable advantage for our students!

The PG Diploma in Clinical Research programme at BCRI includes domains like Clinical Research (CR), Clinical Data Management (CDM), Clinical SAS (SAS), Regulatory Affairs (RA), Pharmacovigilance and Drug Safety (PV), Professional and Career Development (PCD), Practical Training and Internship (PTI).

Certainly! Completing the Post Graduate Diploma in Clinical Research (PGDCR) equips graduates with a robust set of practical skills and competencies that enhance their employability in the clinical research job market. Here are the key areas where PGDCR graduates with BCRI benefits, students learn to handle patient recruitment, data collection, adverse event monitoring, and protocol adherence. Understanding regulatory guidelines is crucial. PGDCR covers topics related to Good Clinical Practice (GCP), ICH guidelines, and local regulations. PGDCR imparts skills in clinical data management, including data entry, validation, and quality control, and learns to use statistical tools for data analysis.

Certainly! In a Post Graduate Diploma in Clinical Research (PGDCR) program, students typically gain hands-on experience through various avenues: like Electronic Data Base Capture (EDC) in clinical data management, Safety Data Base in pharmacovigilance, Case processing, Narrative writing, Statistical Analysis Software (SAS) etc..

Yes, on Successful completion of PG diploma in Clinical Research course, we do have 100% placement Support on 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. till date, we have 100% Placement record.

The duration of the Post Graduate Diploma in Clinical Research (PGDCR) program typically is 7.5 months. However,this may vary slightly depending on the add on. During this period, students gain in-depth knowledge about clinical research methodologies, regulations, and hands on experience. PGDCR a valuable program for those interested in pursuing a career in the clinical research industry.

Trainers with extensive experience and expertise in the field of clinical research contribute significantly to the quality of education. We have trainers with high industry experience and research backgrounds. A well-structured curriculum that covers essential topics in clinical research, including regulatory, data management, and practical skills, is a hallmark of our reputable institution. BCRI organizations often incorporate hands-on training, practical exercises, and internship opportunities to ensure that students gain real-world experience in clinical research settings.

A student with a Postgraduate Diploma in Clinical Research (PGDCR) can explore a variety of job roles within the clinical research industry as Clinical Research Associate (CRA), Clinical Research Coordinator (CRC), Clinical Data Manager (CDM), SAS Programmer, Clinical Trial Manager (CTM), Drug Safety Associate (DSA), Regulatory Affairs Specialist, Medical writer, Site Management Organization (SMO) Coordinator etc.

Sample Certificate

PGDCR BCRI JPG -Bangalore Clinical Research Institute

Reviews From Our Happy Students

Creating Vibrant Career & Secured Future!
Teena Rajan
I have completed Advance PG diploma in Clinical Research and Pharmacovigilance from BCRI. My PV trainer was Dev sir. My CDM trainer was Ishani mam. Dev Sir,is very interacting and he made our class interesting. He is very much knowledged and clears all our doubts. He is good in explaining all concepts. I had an amazing experience . I truly recommend this course from BCRI to all PV aspirants.
Meghna Mahesh
I have done Post graduation diploma in Clinical research and Pharmacovigilance. Classes were very informative and Mayuri ma'am and Samarth sir are very knowledgeable and they have explained each and every word of the clinical research and that made the classes very informative and interesting. Very good institute.
Nikita Jaiswal
I have done my PG diploma in clinical research from BCRI. This complete program of pg diploma was very helpful for me to upskill my self in clinical research domain after my graduation. This course include complete knowledge of clinical research, clinical data management, pharmacovigilance and SAS. Read More
Manasi Phadnis
When I enrolled myself in PG diploma at BCRI, I got to know that we are going to be mentored by Mayuri ma'am for PV. I was really excited and eager to be studying under Mayuri ma'am as I had already read a lot about her in the Google reviews. Read More
Naga Nikhila
My training in BCRI has been great. I have completed my pg diploma in clinical research, clinical data management, pharmacovigilance and RA with excellent support and guidance from the faculty.

🎓 What Our Students Say

Real success stories from our students who have transformed their careers with our PG Diploma in Clinical Research (PGDCR) Training! Watch her testimonials and hear firsthand how our program has helped her secure rewarding opportunity in clinical research, pharmacovigilance, and regulatory affairs.

📢 Why Our Students Love BCRI:
✔ Career-changing learning experience
✔ Expert-led training with real-world case studies
✔ Strong industry connections and placement support

👉 Watch her Story ..

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