Research Associate Director
6 days ago
You will be responsible for:
- Verifying the quality, accuracy, completion, and timeliness of data from trial sites.
- Maintaining trial information using the clinical trial management system.
- Supporting strategies to boost recruitment efforts.
- Performing site close-out visits and other site activities as required.
To be successful in this role, you will require:
- A degree in pharmacy, medical, nursing, biological science, or other health-related disciplines.
- ≥5 years' experience in clinical trial monitoring and/or site management.
- High competence in negotiation and conflict resolution, critical thinking, problem-solving, decision making, and strategic thinking.
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