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data management gcp clinical research ich oncology📋 Description
- Lead scientific aspects of clinical protocol execution
- Serve as the lead Clinical Scientist on the trial team
- Lead medical monitoring in data review and deviations
- Collaborate cross-functionally on protocol and study materials
- Ensure CRF design supports data collection per Protocol
- Provide mentorship to other clinical scientists
🎯 Requirements
- Master’s in life sciences with 3+ years in clinical drug development, or PhD/PharmD/RN
- Solid knowledge of GCP and ICH
- Ability to manage multiple priorities with planning and time management
- Strong analytical skills to interpret trial data and draw conclusions
- Proficient in proposing, designing, and executing clinical studies; authoring ICF/SAPs/CSRs
- Oncology experience preferred; strong communication and leadership
🎁 Benefits
- Global full-service CRO with focus on quality and professional development
- Supportive culture and career growth opportunities
- Client-facing role with autonomy and collaboration
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