Clinical Scientist

Job Summary

A company is looking for a Clinical Scientist to contribute to clinical trial protocols and regulatory activities.

Key Responsibilities

• Develop and create clinical trial protocols and study-level documents
• Support pharmacovigilance and regulatory activities, including meeting preparations
• Conduct clinical data reviews and improve data analysis processes

Required Qualifications

• Advanced degree in life sciences, healthcare, or a clinically relevant field
• 3+ years of experience for Sr. Clinical Scientist; 5+ years for Clinical Scientist
• Familiarity with Good Clinical Practice (GCP) and drug development processes
• Experience in global clinical studies within a pharmaceutical company or CRO
• Proficiency in data collection and reporting systems and tools