Eligibility:

B.Pharm / M.Pharm, Pharm D, B.Sc / M.Sc in Life Sciences and other healthcare graduates

Course Description

The Certificate in Clinical Research & Data Management is a 3-month intensive online program designed to equip learners with both scientific and technical expertise in the areas of clinical trial operations and clinical data handling. The course combines 2 months of Clinical Research fundamentals with 1 month of Data Management training — offering a complete understanding of how clinical studies are designed, monitored, and analyzed.

Learners will gain insights into the global clinical research environment, ethical practices, regulatory compliance, and the vital role of accurate data in clinical trials. With hands-on exposure to data management tools and processes, the course bridges the gap between theoretical knowledge and industry application.

What You’ll Learn From This Course

• Understand the end-to-end process of clinical trial management and monitoring.
• Learn data management workflows including CRF design, data validation, and query resolution.
• Gain knowledge of Good Clinical Practice (GCP) and international regulatory guidelines.
• Understand how clinical data is collected, cleaned, and analyzed for research outcomes.
• Develop professional skills required for roles in CROs, pharma companies, and hospitals.

Certification

After completing the program, participants will receive a Certificate in Clinical Research & Data Management from NexVed Clinical Research Academy. This certification demonstrates your ability to manage clinical operations and handle clinical trial data with accuracy and compliance.

Graduates of this course are eligible for roles such as Clinical Data Manager, Clinical Research Associate (CRA), Clinical Trial Assistant, and Regulatory Affairs Executive. It’s an ideal course for life science and pharmacy graduates seeking to establish a strong career in data-driven clinical research operations.