Medical Director – Oncology Clinical Development

GSK

Medical Director for Oncology Clinical Development at GSK; collaborating on clinical trials for hematological malignancies. Contributes to protocol development, trial execution, and regulatory compliance in oncology drug development.

Posted 6/6/2026full-timeUpper Providence • Massachusetts, Pennsylvania • 🇺🇸 United StatesLead💰 $222,750 - $371,250 per yearWebsite

About the role

Key responsibilities & impact

Collaborate with physicians, scientists, regulatory professionals, biostatisticians, executive staff, and others in a complex matrix environment to develop and execute phase 1-3 interventional clinical trials
Use medical expertise to contribute to the end-to-end (protocol concept to final study report) and timely delivery of clinical trials while ensuring patient safety, scientific integrity, and consistency with the clinical development strategy, for regulatory approvals, payor reimbursement, and successful lifecycle management; demonstrate ability to incorporate global considerations into decision making
Ensure high-quality protocol development aligned with the Clinical Development Plan to effectively determine a medicine’s potential efficacy, safety profile, key areas of product differentiation and value to patient in the shortest possible timeframe.
Assume medical responsibility for clinical trials with active participation in real-time medical monitoring, including patient eligibility assessment, study design questions, and addressing urgent safety questions (with inclusion of Safety/ PV as relevant).
Assume responsibility for medical review of clinical trial data, both directly and/or via oversight of delegated medical review.
Oversee blinded review of data packages intended for IDMCs.
Review/monitor safety data in collaboration with pharmacovigilance group for active clinical studies.
Interpret and summarize study results consistent with objectives to define safety, efficacy, pharmacokinetic/pharmacodynamic, and patient reported outcomes, and applicability of data to the targeted patient population.
Participate in the authoring of clinical study reports and regulatory documents and collaborate with colleagues in Regulatory Affairs, CMC, Toxicology, Research, and Pharmacology to respond to health authority and ethics committee queries.
Collaborate with Principal Investigators in the authoring of publications (abstracts, posters, manuscripts) associated with clinical data.
Network extensively to develop long-term strategic partnerships with thought leaders both internally and externally, in support of GSK’s vision.
Serve as a core member of the Clinical Matrix Team for one or more assets in development.
Participate in Oncology Clinical Development-wide initiatives and workstreams as appropriate.

Requirements

What you’ll need

Medical degree with board certification/eligibility or registration qualifications in medical oncology, hematology or hematology/oncology
Experience in the pharmaceutical/biotechnology industry, clinical academic medicine, or clinical medical practice, in the field of hematology and/or oncology
Oncology clinical drug development experience in the conduct of clinical trials (investigator-initiated, company-sponsored or cooperative group trials) and their subsequent publications

Benefits

Comp & perks

health care and other insurance benefits (for employee and family)
retirement benefits
paid holidays
vacation
paid caregiver/parental and medical leave

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

clinical trialsprotocol developmentmedical monitoringdata reviewsafety data monitoringpharmacovigilanceclinical study reportsregulatory documentsoncology clinical drug developmentpatient eligibility assessment

Soft Skills

collaborationcommunicationnetworkingstrategic partnershipsteamworkdecision makingleadershipproblem solvinginterpersonal skillsorganizational skills

Certifications

medical degreeboard certification in medical oncologyboard certification in hematology