Related skills
gcp edc ich etmf ctms📋 Description
- Lead clinical projects per budget and scope; may run international trials.
- Act as primary client liaison; support proposals and client presentations.
- Liaise with project team and senior management, including C-level.
- Lead all aspects of a clinical trial or trials.
- Oversee data management, safety, clinical, monitoring, and biostatistics.
- Prepare status updates with deliverables and metrics.
🎯 Requirements
- Degree in life sciences or equivalent qualification.
- CRO full-service/global Project Management experience.
- 5-7 years in industry; at least 4 years PM in clinical trials.
- Experience managing oncology studies.
- Knowledge of GCP/ICH guidelines and clinical development process.
- Ability to travel domestically and internationally.
🎁 Benefits
- Supportive, collaborative environment.
- Work-life balance emphasis.
- Opportunities for team development.
- Dynamic, high-energy team culture.
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