Description
As a Clinical Research Coordinator, you will work with researchers to ensure studies are conducted according to regulations, standard operating procedures (SOPs), and good clinical practice (GCP).
Key responsibilities include:
- Assisting researchers with feasibility surveys and case report forms
- Supporting site initiation and monitoring visits
- Managing investigational products, study materials, and laboratory samples
- Coordinating subject screening, enrollment, and follow-up activities
- Maintaining accurate records and reporting study progress
- Collaborating with researchers, monitors, and ethics committees as needed
- Ensuring compliance with regulatory requirements and GCP guidelines
- Performing other tasks as assigned
Requirements:
- Bachelor's degree in a medical or related field (e.g., clinical medicine, pharmacology, nursing, healthcare)
- Clinical research experience is an advantage