Senior Clinical Scientist
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
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