Medical Scientific Director: Evidence Strategy & Studies

BioSpace

Kansas

Hybrid

USD 180,000 - 280,000

Full time

4 days ago
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Job summary

BioMarin is seeking a Medical Scientific Director to oversee day-to-day operations of multiple BioMarin‑sponsored and collaborative studies across therapeutic areas. You will partner with Real World Evidence, Global Medical Leads, and Data Sciences to design practical study strategies and ensure hands-on execution support for medical affairs‑led studies.

The role requires leading scientific input on protocols, statistical plans, data interpretation and regulatory responses, with opportunities to

Qualifications

  • PharmD/PhD/MD with at least 5 years experience conducting observational and Phase IIIb/IV studies or MS/MPH with 10+ years similar experience.
  • Experience delivering a portfolio of protocols aligned to program objectives.
  • Experience addressing regulatory or IRB/Ethics questions about study designs and protocol conduct.

Responsibilities

  • Oversee day-to-day conduct of BioMarin-sponsored and collaborative studies across therapeutic areas.
  • Collaborate with Global Medical Leads, RWE/Epidemiology, Data Sciences and Study Operations to develop study strategies.
  • Provide scientific input into study concepts, protocols, SAPs, and regulatory responses.
  • Coordinate preparation of regulatory submissions and responses to queries.
  • Present study results to internal and external stakeholders and at scientific conferences.

Skills

Cross-functional collaboration
Scientific writing
Study monitoring
Regulatory interaction
Data interpretation

Education

PharmD/PhD/MD or MS/MPH

Job description

BioMarin is seeking a Medical Scientific Director to oversee day-to-day operations of multiple BioMarin‑sponsored and collaborative studies across therapeutic areas. You will partner with Real World Evidence, Global Medical Leads, and Data Sciences to design practical study strategies and ensure hands-on execution support for medical affairs‑led studies.

The role requires leading scientific input on protocols, statistical plans, data interpretation and regulatory responses, with opportunities to

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