This training program is aimed at imparting skills and competencies required for the specialized job function of Clinical Trial Monitor/Clinical Research Associate. By participating and successfully completing this training program, one can specialize in Clinical Trial Monitoring field through a unique hands-on training experience.
Program Highlights
- Self-learning study modules/Matchbook course
- Assignment based evaluation
- Self-paced schedule (1-6 months)
- Training topics
- Introduction to Clinical Research
- Evolution of Ethical Research Principles, Regulations and Guidelines
- Clinical Study Process
- Investigator Site Selection/Assessment
- Development of Monitoring Plan
- Site Initiation, Review of Essential Trial Documents, Delegation of Duties
- Clinical Trial Monitoring
- Inventory Planning and Tracking
- Source Document Verification (SDV)
- CRF Review, Collection and Co-ordination of Data Management Activities
- Escalation, Management and Prevention of Violations/Deviations
- Tracking of Enrolments, Payments and Ongoing Correspondence
- Unique practical training component through "mock hands-on training material"
- Placement assistance through regular job postings (via WhatsApp)
Eligibility
Candidates who are currently pursuing or have completed following curriculum are eligible for enrolment:
- B.Pharm, M.Pharm, PharmD, PhD
- MBBS, MD, DNB, DM
- BDS, MDS
- BAMS, BHMS, BUMS
- BPT, MPT
- Life Sciences: B.Sc, M.Sc, Biotechnology
- Working Professionals
Program Fee
Indian Participants | Rs. 16,000 |
Indian Participants Residing Overseas | Rs. 21,000 |
Foreign Nationals | US$ 375 |