Senior Onco Clinical Development Director (GU)

Regulatory Jobs

Waltham (MA)

Presencial

USD 284.000 - 474.000

Jornada completa

Hace 5 días
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Ventajas ofrecidas por este puesto de trabajo

Annual bonus
Health care benefits
Retirement benefits

Descripción de la vacante

GSK in the US is seeking a Senior Medical Director, Oncology Clinical Development - GU to lead phase 1-3 GU oncology trials and drive regulatory and market activation. The role requires medical oncology expertise, global trial leadership, and collaboration with cross-functional teams across Clinical Development, Regulatory Affairs, and HEOR.

On-site presence at US sites is required. The position offers a competitive base salary (shown below), an annual bonus, and a comprehensive benefits

Formación

  • Medical degree and completion of advanced specialty training in Medical Oncology, Radiation Oncology, Urology or Internal Medicine with GU/oncology experience.
  • Experience leading GU Oncology drug development across Phase 1–3 trials.
  • Academic or clinical publication history in GU Oncology.

Responsabilidades

  • Lead phase 1–3 interventional GU oncology trials and oversee study design, initiation, execution and closure.
  • Represent Clinical Development on disease area strategy and medical affairs initiatives.
  • Collaborate with Regulatory Affairs, CMC, Toxicology and Research to respond to health authority queries.
  • Network with KEEs and external experts to support GSK’s clinical portfolio and business development.

Conocimientos

Clinical Data Interpretation
Clinical Trials Monitoring
Drug Development
Regulatory Affairs
Medical Oncology
Communication

Educación

Medical degree
Advanced specialty training in Medical Oncology

Descripción del empleo

GSK in the US is seeking a Senior Medical Director, Oncology Clinical Development - GU to lead phase 1-3 GU oncology trials and drive regulatory and market activation. The role requires medical oncology expertise, global trial leadership, and collaboration with cross-functional teams across Clinical Development, Regulatory Affairs, and HEOR.

On-site presence at US sites is required. The position offers a competitive base salary (shown below), an annual bonus, and a comprehensive benefits

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