Medical Monitor (Oncology)
Core
Provide medical oversight and expertise for global oncology clinical trials, ensuring participant safety and scientific quality.
Role type
Medical Monitor (Oncology)
Builds
Clinical development plans, protocols, investigator brochures, informed consent documents, annual reports, clinical study reports, patient narratives, and scientific presentations.
Domain
Clinical research / Oncology
Required skills
Medical judgement, analytical thinking, attention to detail, clear communication, presentation skills, collaborative approach, proficiency with clinical trial systems and digital collaboration tools.
Preferred skills
Experience in clinical research or pharmaceutical/CRO industry.
Technologies
Microsoft Office applications, clinical trial systems, digital collaboration tools.
Responsibilities
Serve as primary medical point of contact for sponsors, investigators, and sites; Provide medical oversight throughout trial conduct; Respond to medical questions from stakeholders; Provide medical input into eligibility assessments, protocol deviations, and safety issues; Contribute to clinical development plans and documents; Review and assess clinical and safety data; Prepare and deliver medical training; Support pharmacovigilance activities; Identify trial risks and define mitigation measures; Participate in advisory boards and safety monitoring committees.
Seniority
Mid-level to Senior, hands-on IC