Senior Oncology Clinical Development Leader

GSK

Stevenage, Cambridge

On-site

GBP 213,000 - 356,000

Full time

5 days ago
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Benefits offered by this job

Health care benefits
Retirement benefits
Paid holidays
Vacation
Paid caregiver/ parental leave

Job summary

GSK seeks an experienced Senior Medical Director in Oncology Clinical Development to lead GU programs, design and oversee phase 1–3 trials, and engage with internal and external experts. The role requires managing medical strategies, safety monitoring, and regulatory interactions across a growing oncology portfolio.

The position emphasizes leadership, collaboration, and scientific excellence to advance clinical development, regulatory filings, and eventual market launch, with on-site

Qualifications

  • Medical degree with advanced specialty in Oncology, Radiation Oncology, Urology or Internal Medicine with GU/oncology experience.
  • Experience leading GU Oncology drug development across Phase 1–3 trials.
  • Academic/clinical research publications or medical practice history in GU Oncology.

Responsibilities

  • Lead interventional clinical trials (Phase 1–3) in a cross-functional setting.
  • Develop and execute disease-area and medical affairs strategies.
  • Collaborate with Regulatory Affairs, CMC, Toxicology and others to respond to inquiries.

Skills

Clinical Data Interpretation
Clinical Pharmacology
Clinical Trial Designs
Clinical Trials Monitoring
Hematology and Oncology
Evidence Based Decision Making
Matrix Leadership
Real World Evidence
Strategic Direction
Executive Presence

Education

Medical degree (MD) + advanced specialty training
Fellowship or equivalent specialty training

Job description

GSK seeks an experienced Senior Medical Director in Oncology Clinical Development to lead GU programs, design and oversee phase 1–3 trials, and engage with internal and external experts. The role requires managing medical strategies, safety monitoring, and regulatory interactions across a growing oncology portfolio.

The position emphasizes leadership, collaboration, and scientific excellence to advance clinical development, regulatory filings, and eventual market launch, with on-site

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