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data analysis gcp clinical data management ich oncology📋 Description
- Lead scientific aspects of clinical execution of protocols.
- Serve as the lead Clinical Scientist on the trial team.
- Lead medical monitoring team; review data and deviations with CR/Pharmacovigilance.
- Collaborate cross-functionally on protocol and study materials; partner with Clinical Ops.
- Ensure CRF design supports data collection per Protocol with Clinical Data Management.
- Mentor other clinical scientists and support data analysis and reporting.
🎯 Requirements
- Master’s degree in life sciences + 3 years clinical drug development experience, or PhD, PharmD, RN degree
- Solid knowledge of GCP and ICH regulations
- Ability to manage multiple competing priorities with good planning and time management
- Strong analytical skills to interpret clinical trial data and synthesize conclusions
- Proficient in proposing, designing, and executing clinical studies; authors documents (MMP, SAPs, ICF, CSRs)
- Oncology experience preferred; ability to interact with stakeholders across Clinical Development
🎁 Benefits
- Global CRO with focus on quality and career opportunities
- Client-facing role with independence and collaboration
- Professional development and training
- Supportive culture and teamwork
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