(Associate) Medical Director - Oncology, EMEA at Thermo Fisher Scientific

The Medical Director will provide medical support and advice for clinical trials and safety evaluation within the Pharmacovigilance department. This includes offering medical leadership to study teams, developing clinical trial protocols with the latest scientific information, contributing to site selection, and reviewing/approving study protocols, amendments, Clinical Study Reports, Informed Consent Forms, Case Report Forms, and protocol deviation decisions. They will perform real-time medical monitoring of clinical studies to ensure the medical validity of primary endpoints and subject safety, proactively identifying and correcting medical issues in consultation with the Global Medical Indication Lead. Responsibilities also include liaising between sponsors and internal departments, educating investigator sites, managing day-to-day activities to resolve issues, serving as the medical point of contact for internal and external stakeholders, and ensuring study compliance with all relevant SOPs and GCP by collaborating with cross-functional study team members.