Develop, review, and collaborate on scientific content for clinical documents including protocols, informed consent forms, final study reports, and regulatory submissions.
Oversee patient safety by reviewing risk profiles, monitoring adverse events, and ensuring compliance with safety policies and procedures.
Contribute to investigator selection, lead study start-up training, and provide protocol-specific guidance to investigators and site staff.
Serve as a medical and protocol subject matter expert for clinical operations, monitors, investigators, and ethics committees.
Support data analysis, publication development, and planning/attendance at scientific meetings (e.g., symposia, advisory boards, congresses).
Establish and maintain strategic relationships with external experts and thought leaders.
Monitor competitors, track therapeutic advancements, and stay in...