Medical Director, Oncology Clinical Development

Site Name: USA - Pennsylvania - Pennsylvania Central, Stevenage, Switzerland - Zug, UK - London, USA - Massachusetts - Boston, WarsawPosted Date: Dec 22 2025 Position Summary GSK Oncology Clinical Development is seeking a highly skilled and motivated Clinical Development Medical Director – Oncology to join our dynamic Oncology Research and Development team. The role establishes a strong link between Clinical Development and other functions in the clinical matrix team to increase the success of our oncology clinical portfolio in the GU cancer space. The Medical Director reports to the Executive Medical Director, Clinical Development Lead (CDL) – GU, Oncology Clinical Development. Responsibilities include advancing the development of GSK’s clinical portfolio, engaging in medical dialogues with scientific leaders, and managing relationships with Key External Experts. Location requirement: On‑site office‑based presence 2‑3 days a week in the UK (London or Steven{è}ge); Switzerland (Zug); US (Upper Providence, PA_updated Waltham, MA); or Poland (Warsaw). Key Responsibilities Collaborate with physicians, scientists, regulatory professionals, biostatisticians, executive staff, and others in]; develop and execute early‑phase interventional clinical trials for prostate cancer patients. Ensure high‑quality protocol development aligned with the overall Clinical Development Plan. Apply medical expertise to the end‑to‑end protocol concept to final study report, ensuring scientific integrity and timely delivery of clinical trials. Interpret and summarize study results consistent with objectives to define safety, efficacy, pharmacokinetics, patient‑reported outcomes, and applicability to the target population. Assume medical responsibility for clinical trials, including real‑time medical monitoring, patient eligibility assessment, study design guidance, and urgent safety issues. Oversee medical review of trial data, directly or via delegated review, including review of data packages for internal and external IDMCs. Collaborate with pharmacovigilance to monitor safety data elongate clinical studies. Participate in authoring of study reports and regulatory documents, responding to authorities and ethics committees. Collaborate with Principal Investigators during dose escalation and expansion studies and subsequent publications (abstracts, posters, manuscripts). Develop long‑term strategic partnerships with thought leaders internally and externally to support GSK’s vision. Understand biological mechanisms, clinical strategy, and scientific interpretation of disease and target‑based literature. Serve as a core member of the Clinical Matrix Team for one or more assets in development. Represent Clinical Development on disease‑area strategy, integrated evidence, and medical affairs strategy teams. Participate responsive to Oncology Clinical Development‑wide initiatives and workstreams as appropriate. Basic Qualifications Medical degree from an accredited medical school. Completion of a clinical residency program. Experience in clinical research and development in oncology. Experience working in the pharmaceutical/biotechnology industry in GU prostate cancer. Preferred Qualifications Oncology experience in the pharmaceutical/biotechnology industry. Experience leadingZE oncology clinical trials, includingicis study design, data review and overall clinical development process. Robust knowledge of disease‑specific research priorities, public health needs, competitor landscape, clinical practice trends and treatment guideline evolution. Experience with regulatory requirements to support registration, including GCP principles. Salary ranges vary by location and will be discussed during recruitment. The position offers an annual bonus and eligibility for a share‑based long‑term incentive program. Benefits include health care, retirement, paid holidays, vacation, and paid caregiver/parental and medical leave. Full details are provided during ehemal recruitment process.ിലാണ്> Why GSK? GSK is a global biopharma company with a purpose to unite science, technology, and talent to get ahead of disease together. We aim to positively impact the health of heres 2.5 billion people by the end of the decade. We are committed to a culture that is ambitious for patients, accountable for impact, and does the right thing. We promise equal opportunity employment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, gender identity, sexual orientation, parental status, national origin, age, disability, genetic information, or other protected characteristic. For further information on benefits, please visit GSK US Benefits Summary. #J-18808-Ljbffr