Medical Director, Oncology Clinical Development - Hematology

The Medical Director, Oncology Clinical Development - Hematology role at GSK is focused on advancing cancer treatments through innovative science and strong partnerships. GSK aims to positively impact the health of 2.5 billion people by the end of the decade, with a strong focus on cancers with high unmet needs. The role is based in Stevenage, UK, but will relocate to Cambridge, UK, by early 2029. The main day-to-day responsibilities include providing medical expertise across study design, conduct, safety oversight, and data interpretation. The Medical Director leads medical monitoring activities, ensuring patient safety and clinical integrity. They interpret clinical and safety data, partner with cross-functional teams, and contribute to protocol development. The role also involves engaging with investigators, supporting regulatory interactions, and contributing to scientific communications. To qualify, candidates must have a medical degree and relevant clinical experience. They should be proficient in English and have a strong understanding of clinical trial regulations, including GCP and ICH guidelines. Experience in oncology clinical development is essential, with a focus on hematology. Familiarity with medical monitoring and safety oversight in clinical trials is also required. Nice-to-have skills include experience in protocol development and the ability to engage with key external experts. The role offers the opportunity to work in a dynamic team focused on transforming cancer outcomes. The relocation to Cambridge provides a chance to be part of a growing and innovative environment. What the role asks for: - Medical degree - Relevant clinical experience - Proficiency in English - Understanding of clinical trial regulations, including GCP and ICH guidelines - Experience in oncology clinical development, with a focus on hematology - Familiarity with medical monitoring and safety oversight in clinical trials