Related skills
gcp project management edc clinical trials ichπ Description
- Lead clinical projects within study budget and scope.
- Primary client liaison for proposals and presentations.
- Liaise with project teams and senior management, including C-level.
- Manage all aspects of a clinical trial or trials.
- Oversee data management, safety, clinical, biostatistics, etc.
- Prepare project status updates and key deliverables/metrics.
π― Requirements
- Degree in life sciences or equivalent.
- 5-7 years industry PM experience; 4+ years in full-service CRO.
- Oncology studies management experience.
- GCP/ICH and clinical development process knowledge.
- Ability to travel domestically and internationally, including overnight stays.
- English (written and spoken) and strong presentation skills.
π Benefits
- High-energy, collaborative, dynamic team environment.
- Focus on work-life balance and team development.
- Global CRO with opportunities to lead international trials.
- Equal opportunity employer.
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