Research Study Coordinator Lead
1 day ago
The Clinical Trial Administrator is responsible for performing study-related tasks and ensuring timely production of high-quality clinical data. This individual will work closely with the project team to ensure successful execution of clinical research projects.
Main Duties:
- Document and track study activities using relevant forms and tools.
- Assist in preparing study and site-specific materials.
- Provide support to project team members, including minute taking and documentation.
- Maintain trial master file documentation.
Requirements:
- Diploma or associate degree, or equivalent experience in pharmaceutical or CRO industries.
- Good communication, organizational, and time management skills.
- Computer literacy in Microsoft Office Suite.
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