CDM Internship & Hands-On EDC Training
Gain real-world exposure to clinical research operations, data management, and regulatory documentation through this hands-on internship program.
Duration
30 Days / 45 Days
Course Fee
₹3,499
Course Overview
This internship offers a practical understanding of how clinical research is conducted in the industry. Students will experience various aspects of trial management, documentation, data handling, and regulatory compliance under expert mentorship. It bridges the gap between academic learning and industry expectations.
Key Highlights
- Industry-based practical assignments
- Exposure to Clinical Data Management tools
- Hands-on learning with trial documentation and CRFs
- Guided mentorship from experienced professionals
- Certificate and optional Letter of Recommendation (LOR)
Course Syllabus
Introduction to Clinical Research and GCP
Understanding the fundamentals of clinical research, clinical trial structure, and ICH-GCP guidelines.
Clinical Trial Operations
Learn about trial setup, site management, protocol adherence, and roles of CRA/CRC.
Ethics and Regulatory Framework
Overview of ethical committees, informed consent process, and regulatory submissions.
Clinical Trial Documentation
Detailed training on TMF, eTMF, Case Report Forms (CRFs), and essential documents.
Clinical Data Management
Basics of data collection, data validation, query management, and database locking.
Safety Reporting and Pharmacovigilance
Introduction to adverse event reporting and drug safety monitoring systems.
Industry Tools Overview
Hands-on exposure to EDC tools and trial management systems used in the industry.
Mini Project / Case Study
Work on a real-world project simulating clinical data management and trial workflows.
Assessment and Feedback
Evaluate understanding through tasks, case reports, and mentor feedback.
Career Preparation & Resume Guidance
Learn how to prepare for interviews, write strong resumes, and explore industry roles.
Career Opportunities
Clinical Research Intern
Assist research teams with documentation, data entry, and trial coordination tasks.
Average Salary: ₹2–3 LPA (as entry-level)
Clinical Data Management Intern
Support data management activities including CRF tracking, validation, and quality checks.
Average Salary: ₹2–4 LPA (as entry-level)
Clinical Trial Assistant
Work with project teams to support trial setup, monitoring, and administrative work.
Average Salary: ₹2.5–5 LPA
Regulatory Affairs Trainee
Assist in preparing and submitting documents for regulatory review and approval.
Average Salary: ₹3–6 LPA
Eligibility
- Final-year or recent graduates in Life Sciences, Pharmacy, Nursing, or Biotechnology
- Basic knowledge of clinical research or biology preferred
- Good analytical and communication skills
- No prior work experience required
Certification
Participants will receive a recognized Internship Certificate from Genez Learnings LLP along with an optional Letter of Recommendation (LOR) based on performance.
What Our Students Say
Sathya P.
The internship gave me real exposure to how clinical trials operate. The mentors explained every concept clearly and practically.
Vignesh R.
I learned more in 30 days here than in a full semester at college. The case study and documentation part were very helpful.
Lakshmi S.
This internship helped me understand CDM and GCP deeply. I even got placed in a CRO soon after completing it!
Ready to Transform Your Career?
Join hundreds of professionals who have successfully transitioned into clinical data management roles with our expert-led training programs.