Related skills
gcp edc clinical trials oncology ms project📋 Description
- Independently lead oncology clinical projects across global Ph I-IV trials.
- Oversee all functional areas to meet timelines, scope, cost and quality.
- Act as primary client liaison; support proposals and client presentations.
- Coordinate project team and senior management across Precision and sponsors.
- Manage all trial aspects: data management, safety, clinical, biostatistics.
- Prepare status updates with deliverables and performance metrics.
🎯 Requirements
- Degree in life sciences or equivalent qualification.
- 5-7 years in CRO with 4+ years in full-service PM.
- Experience managing oncology studies in a global CRO.
- Strong knowledge of GCP/ICH and clinical development processes.
- Willingness to travel domestically and internationally.
- Excellent English written and spoken communication.
- MS Office, MS Project, PowerPoint; CTMS, eTMF, EDC, IXRS.
🎁 Benefits
- Supportive, collaborative team environment.
- Strong focus on work-life balance and team development.
- Opportunity to impact precision medicine in oncology.
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