Medical Director, Oncology Clinical Development

GSK

Industrie pharmaceutique

Zug - Schweiz

Responsable de département

Experteer Overview

In this role you will lead clinical data generation and execution of oncology trials to advance GSK’s clinical portfolio. You will work within the Clinical Development team to shape trial strategy, engage with scientific leaders, and build long-term external partnerships. Your medical oversight will drive safety, efficacy, and regulatory support across phase 1–3 studies, contributing to product launches and lifecycle management. This position offers a patient-focused mission in a collaborative, cross-functional environment with global reach.

Rémunérations / Avantages

health care and other insurance benefits (for employee and family)
retirement benefits
paid holidays
vacation
paid caregiver/parental and medical leave
annual bonus and long-term incentive program

Responsabilités

Collaborate in a complex matrix to design and run phase 1–3 interventional trials
Lead high-quality protocol development aligned with the Clinical Development Plan
Ensure scientific integrity from protocol concept to final study report
Interpret and summarize trial data for safety, efficacy, PK/PD, and patient-reported outcomes
Provide medical responsibility for trials, including safety monitoring and eligibility assessment
Oversee medical review of data packages and oversight of blinded IDMC data reviews
Monitor safety data with pharmacovigilance colleagues
Contribute to regulatory documents and respond to health authority queries
Collaborate with Principal Investigators on publications and external communications
Develop long-term strategic external partnerships with thought leaders
Understand disease biology and clinical strategy to support asset development
Serve on Clinical Matrix Team and contribute to disease area strategy and medical affairs
Participate in Oncology Clinical Development initiatives and workstreams

Principales exigences

Medical degree with board certification/eligibility or registration in medical oncology, hematology, hematology/oncology, general surgery, internal medicine, or pathology
Experience in oncology within the pharmaceutical/biotech industry or related clinical settings
Experience in conducting or participating in clinical trials and publications

collaboration across cross-functional teams effective medical communication leadership and strategic thinking clinical trial design and execution (phase 1–3)medical review of trial data regulatory affairs and health authority interactions

Description du poste

In this role you will lead clinical data generation and execution of oncology trials to advance GSK’s clinical portfolio. You will work with…

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