Course Description
The Certificate in Clinical Research & Pharmacovigilance is a 3-month comprehensive online program designed to help students and professionals gain a deep understanding of clinical trials, drug development, and safety monitoring processes. This course combines two essential disciplines — Clinical Research (2 months) and Pharmacovigilance (1 month) — to prepare learners for dynamic roles in the pharmaceutical and healthcare industry.
Participants will learn how clinical trials are planned, conducted, and regulated, while also mastering the fundamentals of drug safety evaluation, adverse event reporting, and global regulatory requirements. With real-world case studies and interactive sessions, this course ensures practical learning and industry readiness.
What You’ll Learn From This Course
- Understand the complete process of clinical trial design, execution, and management.
- Learn regulatory guidelines such as ICH-GCP, Schedule Y, and FDA/EMA frameworks.
- Master the principles of Pharmacovigilance, including case processing and signal detection.
- Develop skills in clinical data documentation, informed consent, and ethics compliance.
- Gain exposure to real-world case studies used in the pharmaceutical and CRO industry.
Certification
Upon successful completion, participants will receive a Certificate in Clinical Research & Pharmacovigilance from NexVed Clinical Research Academy. This certification validates your knowledge and skills, enhancing your employability in roles such as Clinical Research Coordinator, Pharmacovigilance Officer, Drug Safety Associate, and Clinical Trial Assistant.
The course is recognized across the clinical research industry, empowering you to build a strong foundation for a rewarding career in drug development, safety, and regulatory operations.