Build a strong foundation in Clinical Data Management and gain practical, industry-relevant knowledge of the complete CDM lifecycle used in global clinical trials. A structured, 1-on-1 live CDM training programme covering the complete clinical data management lifecycle and built specifically for B.Pharm, M.Pharm, and Life Sciences graduates, and professionals transitioning into CDM from roles like CRA, Pharmacovigilance, or Regulatory Affairs.
This program is ideal for:
• Life Sciences graduates and freshers
• Clinical Research professionals looking to transition into CDM
• CDM professionals seeking a structured refresher
What you'll cover in FCCDM Part 1:
→ Clinical Research Essentials, GCP & ALCOA+ Principles
→ CDM Fundamentals & Clinical Trial Lifecycle
→ Start-Up: Protocol Review, CRF Design, DMP, Edit Checks & UAT
→ Conduct: Data Cleaning, Query Management, SAE Reconciliation & Medical Coding
→ Close-Out: Database Freeze, Database Lock & Archival Activities
→ CDISC Standards Awareness: CDASH, SDTM & ADaM
What's Included:
✔ Live 1-on-1 Personalized Training Sessions
✔ Practical Industry-Based Examples & Exercises
✔ Session Recordings for Revision
✔ Learning Materials & Templates
✔ Certificate of Completion
✔ Doubt-Clearing Support Throughout the Program
✔ All sessions use a single consistent Phase III case study (ZaroMab) so you build real-study intuition, not just theory.
By the end of this program, you will understand the end-to-end Clinical Data Management process and be equipped with the foundational knowledge required to begin or advance your career in CDM.
Note: This is Part 1 of the FCCDM Program and covers Modules 0–4. Career Readiness, Resume Building, LinkedIn Optimization, and Mock Interview Preparation are included in FCCDM Part 2.
On completion: Foundation Certificate in Clinical Data Management (FCCDM)