Medical Director, Oncology Clinical Development - Hematology

• Serve as the physician within the clinical program team, providing medical expertise across study design, conduct, safety oversight, and data interpretation

• Lead medical monitoring activities for clinical studies, ensuring patient safety, clinical integrity, and compliance with the protocol and regulatory requirements

• Interpret clinical and safety data from a physician perspective, generating insights that inform study-level and program-level decisions led by the CDL

• Partner with the Senior Scientist and cross-functional teams to ensure medical considerations are integrated into study execution and delivery

• Contribute medical expertise to protocol development, ensuring clinical relevance, patient safety, and feasibility within the framework defined by the CDL

• Serve as a core member of the Clinical Matrix Team (CMT), providing the medical voice in study-level discussions and cross-functional decision-making

• Engage with investigators and Key External Experts (KEEs) to support study conduct, scientific exchange, and external representation of the program

• Contribute to regulatory documents, Health Authority interactions, and scientific communications from a physician perspective

Medical Monitoring and Safety Oversight

• Lead medical monitoring activities for assigned clinical studies, including real-time clinical decision-making on patient eligibility, protocol-related medical queries, and safety oversight

• Conduct and oversee medical review of clinical trial data, both directly and through oversight of delegated medical review activities

• Interpret and contextualize safety data in collaboration with pharmacovigilance, ensuring appropriate signal detection, escalation, and benefit–risk assessment at the study level

• Participate in safety review forums, including Safety Review Team (SRT) discussions, Independent Data Monitoring Committee (IDMC) data reviews, and internal governance as required

• Ensure medical monitoring activities are conducted in compliance with GCP, ICH guidelines, and applicable regulatory frameworks

Study Design and Execution

• Provide medical input into protocol development, ensuring clinical relevance, patient safety, and operational feasibility within the clinical strategy defined by the CDL

• Apply clinical judgement to support protocol implementation, addressing medical questions that arise during study conduct and ensuring consistency with the study’s scientific objectives

• Partner with the Senior Scientist to ensure that medical considerations are fully integrated into study execution, data generation, and operational delivery

• Contribute to the development and review of key study documents, including the Informed Consent Form (ICF), protocol deviation management plan (PDMP), and study reference manual (SRM)

• Provide medical input into clinical data generation activities, ensuring alignment with study objectives, patient safety considerations, and the Clinical Development Plan (CDP)

Data Interpretation and Scientific Contribution

• Interpret clinical data from a physician perspective, translating findings into insights on safety, efficacy, and patient impact that inform decision-making by the CDL

• Contribute to study-level and program-level data interpretation, supporting the CDL’s assessment of benefit–risk and clinical positioning

• Contribute to the development of scientific communications, including study reports, clinical study summaries, publications, and congress materials

• Collaborate with investigators on the evaluation and development of abstracts, posters, and manuscripts derived from clinical program data

• Maintain current knowledge of the asset’s biological mechanism, disease landscape, evolving treatment paradigms, and competitive environment to inform clinical interpretation

Regulatory and External Engagement

• Contribute medical expertise to regulatory documents and Health Authority interactions, including responses to clinical and safety queries

• Support preparation of materials for regulatory submissions, advisory boards, and external engagements, providing the physician perspective on clinical data and safety

• Engage with Key External Experts (KEEs), investigators, and scientific collaborators to support study conduct, scientific exchange, and relationship development

• Represent the medical perspective at cross-departmental interactions, including Integrated Evidence Team (IET) and Medical Affairs strategy discussions, as delegated by the CDL

• Contribute to the clinical and technical diligence assessment of business development opportunities as requested

Cross-Functional Collaboration and Clinical Matrix Team

• Serve as a core member of the Clinical Matrix Team (CMT), providing medical leadership within study execution

• Contribute medical expertise to disease area strategy, integrated evidence planning, and Medical Affairs discussions as appropriate

• Collaborate across functions — including Clinical Operations, Biostatistics, Regulatory, and Pharmacovigilance — to ensure alignment on study objectives, patient safety, and data quality

• Contribute to Oncology Clinical Development-wide initiatives and workstreams

We are seeking professionals with the following required skills and qualifications to help us achieve our goals:

• MD (or equivalent medical degree) with board certification or eligibility in oncology, hematology, or hematology oncology with experience in treating patients with clonal myeloid disorders.

• Clinical experience in oncology and/or relevant therapeutic areas, with direct exposure to clinical research or drug development

• Experience in clinical trial conduct, including medical monitoring, safety review, and clinical data interpretation

• Experience leading or supporting clinical development activities in accordance with GCP and ICH guidelines and global regulatory frameworks

• Experience applying clinical judgement to support study design, patient safety, and real-time medical decision-making within a structured clinical development framework

• Experience operating effectively within cross-functional matrix teams in a pharmaceutical, biotechnology, or academic clinical trial environment

• Experience translat ing clinical data into clear insights for internal and external audiences

If you have the following characteristics, it would be a plus:

• Experience in pharmaceutical or biotechnology clinical development across Phase I–III oncology studies

• Prior experience contributing to regulatory interactions (e.g., IND submissions, scientific advice, NDA/MAA filings)

• Demonstrated experience engaging with Key External Experts (KEEs), investigators, and scientific collaborators in oncology

• Track record of contributing to clinical publications, congress presentations, or scientific communications

• Deep understanding of oncology disease biology, evolving treatment paradigms, and the competitive landscape across solid tumors and/or hematological malignancies

• Experience in medical monitoring across multiple studies or programs within a clinical development organization

• Familiarity with emerging data and analytics approaches (e.g., real-world evidence, AI-enabled insights) to support clinical interpretation and decision-making

Analytical Thinking, Clinical Data Interpretation, Clinical Development, Clinical Pharmacology, Clinical Trial Designs, Clinical Trials Monitoring, Digital Fluency, Drug Regulatory Affairs, Evidence Based Decision Making, Executive Presence, Hematology and Oncology, Learning Agility, Matrix Leadership, Real World Evidence (RWE), Scientific Presentations

• If you are based in Cambridge, MA; Waltham, MA; Rockville, MD; or San Francisco, CA, the annual base salary for new hires in this position ranges $222,750 to $371,250. The US salary ranges take into account a number of factors including work location within the US market, the candidate’s skills, experience, education level and the market rate for the role. In addition, this position offers an annual bonus and eligibility to participate in our share based long term incentive program which is dependent on the level of the role. Available benefits include health care and other insurance benefits (for employee and family), retirement benefits, paid holidays, vacation, and paid caregiver/parental and medical leave. If salary ranges are not displayed in the job posting for a specific country, the relevant compensation will be discussed during the recruitment process.Polish Salary Range / Polski przedział wynagrodzenia: PLN 455,250 to PLN 758,750The annual gross base salary range for new hires in this position is listed above for each applicable location. These ranges take into account a number of factors including the candidate’s skills, experience, education level and the market rate for the role. In addition, this position may offer an annual bonus and eligibility to participate in our share based long term incentive program which is dependent on the level of the role. More detailed information on the total benefits package will be supplied during the recruitment process. This role is available for applicants from multiple locations, and therefore salary ranges for certain locations are also shown. Salary ranges for other locations are shown because some markets have pay transparency laws that require salary information on job postings, and those locations are potential job sites for this role. If salary ranges are not displayed in the job posting for a specific location or country, the relevant compensation will be discussed during the recruitment process. Please note salaries vary by country based on the candidate’s skills, experience, education level and the market rate for the role. Offers are typically made within the advertised range based on the candidate’s skills, experience and qualifications, with the upper end generally reserved for highly experienced candidates or other exceptional circumstances aligned with these criteria.

Please visit  GSK US Benefits Summary to learn more about the comprehensive benefits program GSK offers US employees.