Job descriptionExecutive Director, Clinical Development Lead - OncologyLocation notes: USA - Pennsylvania - Upper Providence; UK London New Oxford Street; USA - Massachusetts - Boston. Posted Date: Oct 4 2025.At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines, combining our understanding of the immune system with cutting-edge technology to transform people\'s lives. GSK fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing, focusing our efforts on assets that meet patients\' needs and have the highest probability of success. We unite science, technology, and talent to get ahead of disease together.The Executive Director, Clinical Development Lead (CDL) Oncology, will be an integral part of one of the four mechanistic platforms as the single point of accountability for the Clinical Development Plan (CDP). The CDL provides clinical and strategic leadership to the program.Position requirements: This position requires an on-site office-based presence 2 to 3 days a week in one of the following locations: London or Stevenage (UK); Zug (Switzerland); Upper Providence, PA or Waltham, MA (USA); or Warsaw (Poland).ResponsibilitiesAct as the single point of accountability for clinical development plans (CDPs) of an asset. Oversight of disease strategies, indications and associated clinical trial program/study data and integrity.Participate as a core member of the Medicine Development team or Early Development Team and provide a single Clinical Development accountability at the program level within these teams and other cross-functional partnerships with Medical Affairs, Integrated Evidence, Publications, and Global and Regional Commercial functions.Accountable for overall benefit and risk of a clinical program. If not a physician, delegate to and interface closely with an appropriate physician on the program.Lead cross-functional Clinical Matrix Team and provide clinical leadership, Oncology Clinical Development expertise, and customer insight for the program.Guide direct reports to ensure cross-functional integration, coordination, collaboration, and alignment to enable effective and efficient CDP execution.Contribute strategic guidance and highlight clinical considerations to inform portfolio development strategies, individual study design and conduct, combination strategies, and disease area strategies.Interpret complex clinical data and identify trends for clinical and regulatory documents; consult on safety analyses and responses to health authority queries.Prepare for governance discussions in close collaboration with cross-functional Medicine Development Leader (MDL) and other business lines.Manage a team of physicians and/or scientists and allocate resources across the program.Additional responsibilities include:Author and/or review abstracts, presentations and manuscripts for accuracy of clinical data and content.Contribute to the establishment of standards for clinical documents and data review processes across Oncology Clinical Development.Participate in interpretation of data analyses of clinical trial results and support development of clinical study reports.Lead preparation of clinical sections of relevant regulatory filings (IND, study reports, NDA, annual reports, etc.).Serve as program clinical expert for internal and external collaborators, investigators, consultants, and contract resources.Lead and provide clinical support for investigator and consultant meetings (e.g., investigator meetings, clinical advisory boards).Lead recruitment, hiring and training for direct report team roles.Provide direct reports with ongoing coaching, development and leadership; including regular staff meetings, check-ins and 1:1 meetings.QualificationsBasic Qualifications:Advanced degree required: PhD/PharmD.Minimum of 8 years pharmaceutical or relevant scientific/medical/clinical experience; minimum of 5 years in Oncology (clinical development experience in one of the four strategic areas of focus preferred).Cross-functional medicine development knowledge and business acumen.Experience with writing scientific communications with clarity, accuracy, and rigor, compliant with governance of disclosure, publication and principles of scientific exchange.Robust knowledge of Oncology treatment guidelines, therapeutic competitive landscape, clinical development process and drug approval process in major regions.Preferred Qualifications:Medical Degree and Oncology board certification/eligibility/registration.In-depth knowledge of GCP, ICH, FDA, EMEA, NICE and other relevant guidelines and regulations.In-depth knowledge of medical and drug terminology with a sound foundation in pharmacology.Highly effective communication skills; ability to present complex data and strategy to groups at all levels.Comprehensive understanding of product and safety profiles.Broad experience in data analysis, interpretation and clinical relevance (e.g., ISS, ISE, competitor data).Experience leading matrix teams with a track record of high performance.Strong decision-making and creative problem resolution in critical situations.Ability to adapt behaviors and priorities to changing environment and dynamics.Ability to engage in Oncology Clinical Development culture with confidence, impact, integrity and professionalism.Understanding of adverse effects of medicines on patients and ability to address them.Strong negotiating and influencing skills to guide clinical decisions.Why GSK?At GSK, we are committed to creating an inclusive workplace where everyone can thrive. We value innovation, teamwork, and a shared dedication to improving patient lives. If you are ready to lead transformational change in oncology clinical development, we encourage you to apply.For benefits information, please review the benefits program for US employees; note that this is not a live link in this refined description.Equal Opportunity Employer: GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment regardless of race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information, or military status.Accommodation: If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre at 1-877-694-7547 (US Toll Free) or +1 801 567 5155 (outside US).Important notice to Employment businesses/Agencies: GSK does not accept referrals from employment businesses and/or employment agencies for vacancies posted on this site. All agencies must obtain prior written authorization before referring candidates. This description may include CMS transparency reporting requirements if applicable. #J-18808-Ljbffr