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
Global clinical trials for new oncology treatments
Domain
Clinical Research / Oncology
Required skills
Medical Doctor degree, Board certification in Oncology, Practicing Oncologist experience, Clinical research experience, Medical judgement, Analytical thinking, Attention to detail, Communication skills, Presentation skills, Microsoft Office proficiency
Preferred skills
Pharmaceutical or CRO industry experience, Clinical trial systems proficiency
Responsibilities
Serve as primary medical point of contact for sponsors and investigators, Provide medical oversight per protocol and GCP guidelines, Respond to medical questions from trial stakeholders, Provide medical input into eligibility and safety assessments, Contribute to clinical development plans and reports, Review clinical and safety data, Deliver medical training to investigators, Support pharmacovigilance activities, Identify trial risks and mitigation measures, Participate in safety monitoring boards
Seniority
Mid-Senior, hands-on IC
