Senior Oncology Clinical Development Director

GSK; Zug; Hybrid; CHF 180.000 - 300.000; Vollzeit

Benefits dieser Stelle

Health care benefits

Retirement benefits

Paid holidays

Paid caregiver/parental leave

Medical leave

Zusammenfassung

GSK is seeking a Medical Director, Oncology Clinical Development to lead clinical trial programs and drive data generation in oncology. This on-site role requires engagement with key external experts and internal teams to advance development, regulatory filings and market launch readiness across multiple jurisdictions.

The position supports on-site presence 2–3 days per week in UK, Switzerland, US or Poland, with responsibilities spanning protocol design, safety oversight, and cross-functional

Qualifikationen

• Medical degree with board certification/eligibility or registration qualifications in medical oncology, hematology, hematology/oncology, general surgery, internal medicine, or pathology.
• Oncology experience in pharma/biotech, academia, or clinical practice settings.
• Experience in conduct/participation of clinical trials and publications.

Aufgaben

• Develop and execute phase 1–3 interventional clinical trials in a complex matrix environment.
• Ensure high-quality protocol development aligned with the Clinical Development Plan.
• Oversee safety reviews, data interpretation and regulatory documentation collaboration.

Kenntnisse

Analytical thinking

Clinical data interpretation

Clinical development

Medical communication

Ausbildung

Medical degree

Board certification/eligibility in oncology

Registration qualifications in medical oncology/hematology

Jobbeschreibung

GSK is seeking a Medical Director, Oncology Clinical Development to lead clinical trial programs and drive data generation in oncology. This on-site role requires engagement with key external experts and internal teams to advance development, regulatory filings and market launch readiness across multiple jurisdictions.

The position supports on-site presence 2–3 days per week in UK, Switzerland, US or Poland, with responsibilities spanning protocol design, safety oversight, and cross-functional