Medical Director, Oncology Dev – Lung & Head/Neck (On‑Site)

WIB-Pittsburgh; Collegeville (PA); On-site; USD 223,000 - 371,000; Full time

Job summary

GSK, a global biopharma company, seeks a Medical Director in Oncology Clinical Development for Lung & Head/Neck cancers. This on-site role focuses on medical leadership across study design, safety oversight, and data interpretation within the clinical development framework.

The position requires MD with oncology certification, extensive clinical trial experience, and strong cross-functional collaboration to drive safe, high-quality programme delivery.

Qualifications

• MD with board certification or eligibility in oncology.
• Clinical trial experience with medical monitoring, safety oversight.
• Ability to translate clinical data into actionable insights for decision-making.
• Experience working in cross-functional matrix teams within pharma/biotech.

Responsibilities

• Serve as physician within the clinical programme 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 regulatory compliance.
• Interpret clinical and safety data to inform study-level and programme-level decisions.
• Collaborate with cross-functional teams to ensure medical considerations are integrated into study execution and delivery.
• Contribute to regulatory documents and Health Authority interactions from a physician perspective.

Skills

Oncology expertise

Clinical monitoring

Data interpretation

Cross-functional collaboration

Regulatory awareness

Education

MD or Doctor of Medicine

Job description

GSK, a global biopharma company, seeks a Medical Director in Oncology Clinical Development for Lung & Head/Neck cancers. This on-site role focuses on medical leadership across study design, safety oversight, and data interpretation within the clinical development framework.

The position requires MD with oncology certification, extensive clinical trial experience, and strong cross-functional collaboration to drive safe, high-quality programme delivery.