Job Summary
A company is looking for a Clinical Project Coordinator to assist with project management and site management for clinical studies.
Key Responsibilities:
- Support day-to-day management of studies, ensuring timely delivery of project tasks within budget and compliance with expectations
- Assist in document management, including the creation, review, and filing of essential study documents
- Participate in project meetings and support query resolution, audits, and regulatory submissions
Required Qualifications:
- Bachelor's degree in a biomedical-related field, life sciences, or equivalent
- Profound knowledge of Good Clinical Practice and relevant regulatory requirements
- Strong organizational and time management skills
- Commitment to continuous training and knowledge sharing in clinical research
- Ability to work independently and as part of a team
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