Clinical Research Project Manager Training
Gain mastery over the entire lifecycle of oncology clinical trials, from site start-up and Phase II trial design through to budgeting, patient enrolment, quality control, and safety monitoring. This equips you with the confidence and skills for Clinical Research Project Manager roles in clinical medicine, ready for promotions and high-impact responsibilities in Nigeria's growing research sector.

from 4 to 360h flexible workload
valid certificate in your country
What will I learn?
This training equips you with hands-on skills to manage oncology clinical trials effectively from initiation to completion. Key areas include smart site selection, IRB processes, boosting patient enrolment, precise budgeting and cost management, strong governance, and risk-based monitoring approaches. You get practical tools, templates, and step-by-step workflows to enhance trial timelines, data accuracy, patient safety, and overall success in a compact, results-driven programme.
Elevify advantages
Develop skills
- Master site start-up: speed up feasibility checks, IRB approvals, and site activation.
- Design Phase II oncology trials: create efficient, FDA-compliant colorectal cancer studies.
- Optimise enrolment: predict rates, increase accrual, and handle weak sites.
- Control budgets: prepare, bargain, and adjust costs for complex oncology trials.
- Oversee quality and safety: use RBM, CAPA, and PV for trials ready for audits.
Suggested summary
Before starting, you can change the chapters and workload. Choose which chapter to start with. Add or remove chapters. Increase or decrease the course workload.What our students say
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