Clinical Trial Manager
Full Time5 hours ago
Employment Information
GCP & Regulatory Compliance
Risk-Based Monitoring
Site Initiation & Close-Out
Sponsor Oversight
Trial Coordination & Monitoring
SIVs, interim visits, close-outs • Source data verification • SAE reporting • ISF/TMF maintenance • Remote monitoring
Quality Assurance
Internal audits • External inspection readiness • CAPA implementation • SOP development • Training delivery
Regulatory & Ethics
Ethics submissions • Regulatory compliance • Protocol adherence • Public trial registry updates
Sponsor Responsibilities
Primary contact for Unit-sponsored trials • DSMB/TSC coordination • Risk assessment • Green-light process
Essential Requirements
- Bachelor’s in health-related field (Nursing, Pharmacy, Medicine, etc.)
- Master’s or Postgraduate Diploma in Clinical Trials
- GCP & Human Subjects Protection certified
- 3+ years clinical trial monitoring experience
- 3+ years active research experience
- Proven audit/inspection experience
- Deep knowledge of ICH-GCP & local regulations
Excellent training & communication skills
How to Apply
Apply online ONLY via the official MRC Uganda portal
Required: 4-page CV + 500-word motivation statement
Deadline: 4 December 2025
Jobxz.com — Uganda’s Premier Platform for Clinical Research Careers • 2025
Share this
Similar jobs
More Jobs Like This
View All Jobs
Opportunities delivered.
Straight to you.
