GSK
Pharmaceutical
MedicalDirector-OncologyClinicalDevelopment
Neural analysis suggests this role is
optimal for Director candidates.
“Medical Director - Oncology Clinical Development at GSK. Skills: Oncology clinical development, Hematological malignancies, Clinical trials. Collaborate to develop and execute phase 1-3 interventional. Use medical expertise to contribute to end-to-end delivery”
What You'll Achieve.
Accelerate significant assets; Meet patients’ needs; Highest probability of success; Timely delivery of clinical trials; Successful lifecycle
Industry & Context.
Minimum two days a week office presence
What They're Looking For.
Must Have
Medical degree with board certification/eligibility or registration qualifications in medical oncology, hematology or hematology/oncology, Experience in pharmaceutical/biotechnology industry, clinical academic medicine, or clinical medical practice, in hematology and/or oncology, Oncology clinical drug development experience in conduct of clinical trials and publications
Nice to Have
MD / PhD preferred, Clinical experience managing patients with hematological malignancies, Oncology clinical research and drug development experience focused on hematological malignancies, including multiple myeloma, Sound understanding of biological mechanisms, clinical strategy, scientific interpretation of disease and target-based literature, Robust knowledge of disease-specific research priorities, public health needs, competitor landscape, clinical practice trends, and treatment guidelines evolution
What You'll Do.
Collaborate to develop and execute phase 1-3 interventional
Use medical expertise to contribute to end-to-end delivery
Ensure patient safety
Ensure high-quality protocol development aligned with Clinical Development
Determine medicine’s potential efficacy
Assume medical responsibility for clinical trials
Participate in real-time medical monitoring
Assess patient eligibility
Address urgent safety questions
Assume responsibility for medical review of clinical trial
Oversee blinded review of data packages
Review/monitor safety data in collaboration with pharmacovigilance
Interpret and summarize study results
pharmacokinetic/pharmacodynamic
and patient reported outcomes
Summarize applicability of data to targeted patient population
Participate in authoring clinical study reports and regulatory
Respond to health authority and ethics committee queries
Collaborate with Principal Investigators in authoring publications
Network to develop strategic partnerships with thought leaders
Serve as core member of Clinical Matrix Team
Participate in Oncology Clinical Development-wide initiatives
How You'll Work.
Team & Collaboration
Complex matrix environment; Multi-disciplinary team; Clinical Matrix Team; Cross-functional collaboration
Communication Scope
Authoring publications; Responding to queries
Full Job Description
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, 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. Find out more: [Our approach to R&D](https://www.gsk.com/en-gb/innovation/) The Medical Director, Oncology Clinical Development will report to the Executive Medical Director / Clinical Development Lead (CDL), Oncology Clinical Development. This position will support our growing oncology portfolio for the treatment of hematological malignancies. The Medical Director will have the opportunity to work across early- to late-stage development and in partnership with a multi-disciplinary team of oncology drug developers. **An on-site office presence for a minimum of two days a week is required in one of GSK’s UK (London or Stevenage), US (Greater Philadelphia or Waltham), Switzerland (Zug) or Poland (Warsaw) campuses.** **Key Responsibilities** * 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 decisi
Applying for this Medical Director - Oncology Clinical Development role?
Most applicants get filtered before a human reads their resume. See if yours makes the cut.
How to Apply on Workday
- Workday has a multi-step form — save your progress after every section.
- "Apply With LinkedIn" can fail or lose data; manual entry is more reliable.
- Watch for the "Submit for Review" final step — hitting "Save" alone does not submit.
- Job requisition numbers are useful when following up with HR by email.
ANONYMOUS · UNFILTERED
What do employees actually say about GSK?
Real rants from real employees. Read before you apply.