Senior Clinical Scientist

Job Summary

A company is looking for a Senior Clinical Scientist to contribute to clinical trial protocol development and regulatory documentation.

Key Responsibilities

• Develop and create clinical trial protocols and study-level documents
• Support pharmacovigilance and regulatory activities, including preparation for meetings with regulatory agencies
• Perform clinical data review and provide insights for data review process improvements

Required Qualifications, Training, and Education

• Advanced degree in life sciences, healthcare, or a clinically relevant field
• 8+ years of experience for Senior Clinical Scientist; 5+ years for Clinical Scientist
• Familiarity with Good Clinical Practice (GCP) and drug development processes, preferably in Oncology/Immuno-Oncology
• Experience in global clinical studies within a pharmaceutical company, CRO, or academic research institution
• Proficiency in data collection and reporting systems, with a focus on continuous improvement