Related skills
gcp project management edc clinical trials ichπ Description
- Lead clinical projects within budget and scope; may run international trials.
- Primary client liaison; lead proposals and client presentations.
- Coordinate with project team and senior management, including C-level.
- Lead all aspects of a clinical trial or trials.
- Oversee all functions: data mgmt, safety, clinical, biostatistics.
- Prepare status updates with key deliverables and metrics.
π― Requirements
- Degree or life science qualification, or equivalent
- Experience in a full-service/global PM role in CRO
- 5β7 years industry experience; at least 4 years PM in clinical trials
- Experience managing Oncology studies
- Working knowledge of GCP/ICH guidelines and clinical development
- Ability to travel domestically and internationally
π Benefits
- Collaborative, high-energy team environment
- Work-life balance and professional growth
- Opportunity to contribute to precision medicine in oncology
- Global, cross-functional, remote-friendly team
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