Medical Director, Oncology Clinical Development

Das ist der Job

Develop high quality protocols aligned with the Clinical Development Plan to determine efficacy, safety, and value.

Darum lohnt es sich

Key Responsibilities Collaborate with cross‑functional teams to develop and execute phase 1‑3 interventional clinical trials. Contribute to disease‑area strategy and integrated evidence/medical affairs teams.

Medical Director, Oncology Clinical Development Responsible for clinical research activities and medical dialogue for GSK’s oncology antibody drug conjugate portfolio, supporting early to late stage development. Lead end‑to‑end study design, execution, and reporting to ensure scientific integrity and timely delivery.

Interpret and summarize study results on safety, efficacy, pharmacokinetics, and patient outcomes. Assume medical responsibility for trials, including patient eligibility, study design questions, and urgent safety issues. Oversee medical review of clinical trial data; collaborate with IDMC and pharmacovigilance.

Participate in authoring study reports and regulatory documents; respond to health authority and ethics committee queries. Collaborate with Principal Investigators on publications (abstracts, posters, manuscripts). Build strategic partnerships with external thought leaders. Engage in Oncology Clinical Development‑wide initiatives and workstreams.

Basic Qualifications Medical degree with board certification/eligibility in medical oncology, hematology, gynecologic oncology, general surgery, or internal medicine. Experience in oncology cli