OverviewGSK Greater London, England, United KingdomJoin to apply for the Director, Clinical Scientist- Oncology role at GSKSite Name: USA - Massachusetts - Waltham, Switzerland - Zug, UK - United Kingdom, Upper Providence, WarsawPosted Date: Sep 16 2025Director Clinical Scientist- OncologyAt 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, making sure that we focus our efforts on accelerating significant assets that meet patients’ needs and have the highest probability of success. We’re uniting science, technology, and talent to get ahead of disease together.ResponsibilitiesThe Director, Clinical Scientist, Oncology has accountability for providing clinical input during protocol development, oversight of study conduct, and interpretation of study results consistent with objectives to define safety, efficacy, pharmacokinetic/pharmacodynamic, and patient reported outcomes, and applicability of data to the targeted patient population.Lead a clinical matrix team and ensure patient safety is of paramount importance during the study lifecycle; ensure study objectives fulfil regulatory and reporting requirements; support medical governance through the Medical Director and/or the Clinical Development Lead and other Study Team members/stakeholders.Design and execute, in collaboration with the Medical Director, the clinical trial(s) assigned to the project; engage and influence a diverse scientific community of internal and external experts, including collaborations; may manage other staff within Clinical Sciences.Note: This position requires on-site presence 2 to 3 days a week in the UK (London or Stevenage); Switzerland (Zug); US (Upper Providence, PA; Waltham, MA or Boston, MA); or Poland (Warsaw).AccountabilitiesAccountable for Phase 1-4 study design, including clinical pharmacology study designs supporting the CDPUnderstand objectives around safety, efficacy, endpoints, biology, pharmacology, toxicology, biomarkers, and data-driven phenotypesAuthor the Clinical Study Proposal (CSP), prepare and present the study at Protocol Review Forum (PRF), and incorporate governance feedbackEnsure study protocol reflects input from internal and/or external experts and thought leadersCollaborate with functions to ensure the study evaluates key aspects of the Asset Product ProfileProvide input into regulatory documents and ensure timely regulatory reportingLead or participate in regulatory interactions and ensure quality communications with study sitesInterpret study data for clinical study reports (CSRs) and regulatory submissions; ensure input from experts is reflectedCommunicate results to internal/external stakeholders and regulatorsDrive content of clinical documents (e.g., Investigator Brochure) and regulatory documents (DSURs, BRMP, DCSI, Annual Safety Reports, PBRs)Lead completion/filing of key components of clinical modules for regulatory submissionsPrepare and present data for external dissemination (abstracts, posters, conference presentations)Engage in advisory boards and scientific engagement activities; deliver end-of-study reportsQualificationsBasic QualificationsBachelor’s degree in Life Science or equivalent2+ years of pharma industry or relevant clinical trial experience2+ years of clinical trial and clinical research experience; running clinical trials in early or late phasesExperience in a matrix management and large cross-functional team environmentExperience generating clinical Protocols and ICFsExperience working with data management and data cleaning of clinical dataPreferred QualificationsAdvanced degree (e.g., MS, PhD, PharmD, RN) or equivalent experienceOncology or immuno-oncology experience preferredAbility to build internal and external relationships in a dynamic, matrixed environmentStrong communication skills tailored to the audience; good knowledge of disease-specific research priorities and regulatory landscapeBroad understanding of pharmaceutical development and regulatory requirementsDemonstrated leadership in cross-functional clinical development and program deliveryExperience across study, project, and program levels; ability to work across multiple projectsAwareness of business drivers and alternative delivery solutions; strong interpersonal skillsKnowledge of worldwide regulatory and safety requirements; experience leading in matrix and line environmentsWhy GSKGSK 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 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases. We are committed to creating an environment where our people can thrive and focus on what matters most.If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre for accessibility support.GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, pregnancy, gender identity, sexual orientation, parental status, national origin, age, disability, genetic information, military service or any basis prohibited under law.Seniority levelNot ApplicableEmployment typeFull-timeJob functionHealth Care ProviderIndustries: Pharmaceutical ManufacturingNote: Referrals may not be required to apply; information regarding benefits may be provided by the employer as part of recruitment communications. #J-18808-Ljbffr