Medical Director, Oncology Clinical Development (Medellín)
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Medellín, Colombia
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Publicado: hace menos de una semana
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- Collaborate with physicians, scientists, regulatory professionals, biostatisticians, executive staff, and others to develop and execute phase 1-3 interventional clinical trials.
- Use medical expertise to contribute to end‑to‑end protocol development and timely delivery of clinical trials, ensuring patient safety, scientific integrity and alignment with clinical development strategy.
- Ensure high‑quality protocol development aligned with early Clinical Development Plan to assess medicine’s efficacy and safety profile.
- Assume medical responsibility for early‑phase clinical trials, actively monitoring patient eligibility, study design, and urgent safety issues.
- Review medical data from clinical trials directly or through delegated oversight.
- Monitor safety data in collaboration with pharmacovigilance group for active studies.
- Interpret and summarize study results to define safety, efficacy, PK/PD, patient‑reported outcomes, and relevance to target population.
- Co‑author clinical study reports and regulatory documents, responding to health authority and ethics committee queries with cross‑functional teams.
- Collaborate with Principal Investigators on publications (abstracts, posters, manuscripts).
- Network extensively to build long‑term strategic partnerships with thought leaders internally and externally.
- Serve as core member of the Early Development Team for one or more assets.
- Participate in Oncology Clinical Development‑wide initiatives and workstream Postúlate en Kit Empleo: kitempleo.com.co/empleo/1avg9v
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Nombre de la empresaGlaxoSmithKline
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Nombre de la vacanteMedical Director, Oncology Clinical Development (Medellín)
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