Manager, Central Monitoring - FSP
Parexel · South Africa
Clinical Research
Remote
Not yet analysed
Demand78
Career growth76
Healthcare fit72
Remote potential55
5-year outlook
Manager-level CRO clinical research roles generally offer stable compensation and progression into program-level RBQM, central monitoring leadership, or clinical operations management. Exact salary depends on location, sponsor, and prior central monitoring experience.
Clinical license
Not required
Applicant reach
moderate
Seniority
senior
Employment type
full-time
Date found
2026-11-09
Intelligence details
Flexible work details
- Engagement type
- Contract
- Hours
- Variable hours
- Rate period
- Annual
Why this was classified this way
- Contract
Listing via Himalayas.
Eligibility, licensing, and location restrictions can change. Always confirm details on the source posting before applying.
Why this is worth applying to
Worth considering if you already have clinical trial monitoring, study coordination, data review, or RBQM experience and want to move deeper into centralized risk-based monitoring. It is not an entry-level transition for clinicians without clinical research exposure.
Who should apply
Clinicians with CRO, sponsor, or site-level clinical research experience, especially CRAs, research nurses, study coordinators, pharmacists, or medically trained professionals who have worked with clinical trial data review, risk assessment, or quality management.
CV angle
Frame real clinical research and trial experience around RBQM, central monitoring, KRI/KPI interpretation, protocol and ICH-GCP knowledge, risk assessment, data trend review, cross-functional study team collaboration, and process improvement. Do not claim central monitoring ownership unless you have genuinely performed it.
Skills to highlight
- Risk Based Quality Management
- Central Monitoring
- KRI/KPI Analysis
- Clinical Trial Operations
- Risk Assessment
- Clinical Data Review
- ICH-GCP
- Cross-Functional Collaboration
Role summary
A manager-level clinical research role leading centralized monitoring for global and complex trials, using KRI/KPI data and operational trends to identify risks, support study teams, author central monitoring plans, and strengthen RBQM execution.
We publish our own intelligence summary, never the full job description. Always confirm details with the employer when you apply.