Medical Scientific Director, Observational Studies Leader

BioMarin Pharmaceutical Inc.; Greater London; Híbrido; GBP 110.000 - 165.000; Tempo integral

Resumo da vaga

BioMarin Pharmaceutical Inc. in London (hybrid) seeks a Medical Scientific Director to oversee day-to-day management of multiple studies, ensuring consistent conduct and robust data interpretation.

You will partner with Real World Evidence, Global Medical Leads, and Data Sciences to develop practical strategies and support Medical Affairs-led studies. The role requires advanced clinical research experience, strong scientific writing skills, and a track record of cross-functional collaboration to

Qualificações

• PharmD/PhD/MD with at least 5 years experience conducting observational and Phase IIIb/IV studies within Clinical Development and/or Medical Affairs.
• MS/MPH with 10+ years similar experience.
• Experience delivering a portfolio of protocols and regulatory responses.

Responsabilidades

• Oversee study strategy and implementation across multiple programs within Medical Affairs and Integrated Evidence.
• Collaborate with Global and Country Medical Leads, RWE, HEOR and Data Sciences to shape plans.
• Provide scientific input on study concepts, protocols and regulatory responses; present results to stakeholders.
• Coordinate regulatory submissions questions and ensure data interpretation and reporting quality.
• Drive efficiency in study execution and maintain high standards of medical monitoring.

Conhecimentos

Cross-functional collaboration

Scientific writing

Study design

Clinical research

Data interpretation

Regulatory submissions

Formação

PharmD/PhD/MD

MS/MPH

Descrição da vaga

BioMarin Pharmaceutical Inc. in London (hybrid) seeks a Medical Scientific Director to oversee day-to-day management of multiple studies, ensuring consistent conduct and robust data interpretation.

You will partner with Real World Evidence, Global Medical Leads, and Data Sciences to develop practical strategies and support Medical Affairs-led studies. The role requires advanced clinical research experience, strong scientific writing skills, and a track record of cross-functional collaboration to