Job Summary
A company is looking for a Project Management Specialist, Optimized Trials.
Key Responsibilities
- Supports project setup, maintenance, and closeout of clinical trial files and regulatory documents
- Tracks project milestones and submission timelines, providing rationale for any delays and assisting with contingency plans
- Facilitates team meetings, prepares meeting minutes, and ensures compliance with regulatory requirements
Required Qualifications
- BS/BA in Life Science or related discipline
- Minimum of one (1) year clinical research experience or experience in a healthcare setting
- Previous GCP training and certification is preferred
- Experience with electronic medical records and data entry is preferred
- Strong computer skills, including knowledge of CTMS and MS Office products
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