Medical Monitor

Job description

About this role TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full-service capabilities, resourcing, and Functional Service (FSP) solutions. The Medical Monitor ensures participant safety, oversees clinical trial protocols, and maintains data integrity throughout the research process. As part of our SRS/FSP team, you will be dedicated to one sponsor, a global pharmaceutical or biotechnology company that is an industry leader within its therapeutic area. Key Responsibilities: Provide medical consultation on study-related matters, including participant eligibility, protocol-related questions, efficacy and safety procedures, concomitant medication, adverse events, and SAE reporting. Review SAE narratives and support the early identification of safety concerns across clinical studies. Review and classify protocol deviations and assess exclusionary or alert laboratory values, as well as other relevant testing data. Support the medical review of participant data listings, patient profiles, and medically coded term...