Job Description
Responsibilities:
- Assist in the planning and execution of clinical research studies.
- Coordinate and oversee the collection, analysis, and interpretation of study data.
- Ensure compliance with study protocols, regulatory requirements, and ethical standards.
- Conduct site visits to monitor study progress and ensure adherence to study procedures.
- Manage study documentation, including case report forms and informed consent documents.
- Collaborate with study investigators and study team members to ensure smooth study operations.
- Conduct training sessions for study site personnel on study procedures and requirements.
- Prepare study reports and contribute to the development of study protocols and study-related documents.
- Stay updated on relevant regulations, guidelines, and industry best practices in clinical research.
Requirements
- Bachelor's degree or ...