Director, Oncology Clinical Development Physician (Early)

Location of role Gaithersburg, MD, Radnor, PA, Oxford, UK Department Clinical Development Key Responsibilities Main Purpose of Job: This role will contribute to advancing both the oncology programs in various stages of development and the fabric of Immunocore’s clinical sciences. The successful candidate will lead and facilitate Clinical Development strategic planning and be accountable for the design and medical oversight of clinical studies, including protocol development, medical monitoring, medical data review, results interpretation, reporting and regulatory submissions. In addition, they will lead innovation in trial design, including development of biomarker strategies. This role will be a key in-house oncology disease area expert for R experience in immuno-oncology highly desirable At least 3 years of relevant experience in clinical drug development across academia or pharmaceutical industry (must include experience conducting early phase trials) 2 years or more experience as a medical monitor in a biotechnology/ pharmaceutical company, and/or CRO. Demonstrated ability to build mutually respectful relationships with colleagues. Trouble shoot challenges and provide direction, guidance, and support to the team to deliver on near term goals Strategic and critical thinker, with proven success in designing innovative clinical trials that have supported successful regulatory filings Established links with the medical community globally and locally, with proven ability to develop close working relationships with opinion leaders Strong communication skills, professional presence, and ability to engage effectively with stakeholders at all levels Collaborative and able to motivate and energize cross functional team members to achieve aggressive goals Strong problem-solving, and analytical skills, able to facilitate discussions among groups with diverse technical expertise, and progress decisions on low to moderate complexity issues Working knowledge of GCP, ICH, GDP and relevant CFRs is required; familiarity with MHRA/EMA/CHMP regulations and guidelines and other international regulatory requirements is a plus Thorough understanding of the drug development process including experience contributing to the development of key clinical documents (e.g., protocols, ICF, IB, DSUR, CRF) and ability to review and interpret clinical data About the Company Immunocore (NASDAQ: IMCR) is a pioneering, commercial-stage T cell receptor biotechnology company whose purpose is to develop and commercialize a new generation of transformative medicines which address unmet patient needs in oncology, infectious diseases and autoimmune disease. Our leaders in R it embodies our shared identity and drives our mission. We are dedicated to developing breakthrough therapies that transform patients’ lives, advancing medicine, and supporting one another in these pursuits. Immunocore is proud to be an equal opportunity employer. As such, we are committed to fostering an inclusive workplace where everyone feels valued, respected, and empowered. We encourage applications from individuals of all backgrounds, regardless of race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, or any other characteristic protected by law. #J-18808-Ljbffr