b Overview /b p As Director, Clinical Science in Oncology Clinical Development, you will provide scientific leadership across study design, data review, and interpretation within an asset-level strategy. You will collaborate with the Clinical Matrix Team to align study objectives and ensure high-quality clinical and regulatory documents. Your deep oncology expertise will drive rigorous data interpretation and informed decision-making across trials. This is a hands-on, scientific IC role that supports cross-functional delivery in a matrix environment. You will contribute to scientific excellence and engage with investigators and external experts to advance cancer programs. /p b Pay / Benefits /b ul li health care and other insurance benefits /li li retirement benefits /li li paid holidays /li li vacation /li li paid caregiver/parental leave /li li medical leave and long-term incentive programs (bonus and equity) /li /ul b Responsibilities /b ul li Provide scientific leadership for study design, data review, and interpretation within CDL-guided strategy /li li Serve as core member of Clinical Matrix Team ensuring alignment of objectives, timelines, and deliverables /li li Inform asset-level strategy and programme decisions with scientific insights to support benefit–risk assessments /li li Ensure quality and consistency of clinical/regulatory documents (protocols, IBs, CSRs, submissions) /li li Analyze and interpret data to generate insights on safety, efficacy, and patient populations /li li Engage with investigators and external experts to support study execution and scientific exchange /li li Contribute to culture of scientific excellence, innovation, and continuous improvement in Oncology Clinical Development /li li Author or co-author key study documents and participate in governance forums such as Protocol Review Boards /li li Support study-level Go/No-Go criteria within CDL framework /li li Collaborate across Clinical Operations, Statistics, Safety, Regulatory, and Medical Affairs to enable integrated study delivery /li /ul b Key requirements /b ul li Bachelor’s degree in life sciences or related discipline /li li 5+ years in pharma/biotech or clinical development with oncology focus /li li Experience in clinical development from early stage to regulatory submission /li li Experience with GCP, ICH and global regulatory guidelines /li li Experience authoring/contributing to protocols, IBs, CSRs, and regulatory submissions /li li Experience in cross-functional matrix teams and clinical decision-making /li li Proven track record working with investigators, sites, external experts, CROs, and vendors /li /ul ul li Collaborative mindset /li li Strong scientific communication /li li Cross-functional influencing and partnership /li li Clinical trial design /li li Data review and interpretation /li li Regulatory submission knowledge (IND, NDA/BLA, etc.) /li /ul
Director, Clinical Science – Oncology Clinical Development employer: GSK
GSK is an exceptional employer, offering a dynamic work culture that fosters collaboration and innovation in the heart of Stevenage. With a strong commitment to employee growth, you will have access to extensive development opportunities while working on groundbreaking medicine projects. The hybrid work model and future relocation to Cambridge provide a unique advantage, ensuring a vibrant environment for both personal and professional advancement.
