Job Description
1. Coordinating and managing clinical trials from start to finish.
2. Recruiting, screening, and enrolling study participants.
3. Ensuring informed consent is obtained and documented.
4. Monitoring participant health and providing necessary care during trials.
5. Maintaining accurate and timely documentation of study activities.
6. Preparing and submitting regulatory documents for Institutional Review Board (IRB) approval.
7. Conducting Study Feasibility.
8. Collecting and analysing research data.
9. Managing research budgets.
Communicating with participants regarding study objectives.
Administering questionnaires and monitoring participant adherence to study rules. " Managing Oncology and Cardiology trails
No Referrers Available
There are currently no referrers available for this job. You can still apply, will let you know once there is any referrer available.