Endocrinology Medical Director - Global Clinical Development

Regeneron Pharmaceuticals, Inc.

Washington (District of Columbia)

On-site

USD 285,000 - 386,000

Full time

14 days+

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Job summary

Regeneron Pharmaceuticals, Inc. is seeking a Medical Director to lead endocrinology clinical development. You will guide global study teams, oversee patient safety and regulatory compliance, and lead protocol development. This role requires MD-level expertise and endocrinology board eligibility or certification.

You will collaborate with cross-functional partners to drive program goals, shape future targets, and contribute to publications and data reviews. On-site position with global impact.

Qualifications

  • MD or equivalent with Endocrinology board eligibility or board certification preferred.
  • Pharmaceutical industry experience (2+ years) is desired.
  • Experience with rare disease drug development and CTD submissions in an ICH region is an advantage.

Responsibilities

  • Guide the Global Clinical Study Team to deliver high-quality trials on time.
  • Oversee medical monitoring of clinical trials to ensure patient safety and regulatory compliance.
  • Lead clinical study and protocol development and present to internal and external stakeholders.
  • Provide clinical and scientific leadership for data review, study reports, and publications.
  • Collaborate with cross-functional partners to advance program goals and deliverables.
  • Help shape future targets and development opportunities in the field with discovery teams.

Education

M.D. or equivalent
Endocrinology board eligibility/certification

Job description

Regeneron Pharmaceuticals, Inc. is seeking a Medical Director to lead endocrinology clinical development. You will guide global study teams, oversee patient safety and regulatory compliance, and lead protocol development. This role requires MD-level expertise and endocrinology board eligibility or certification.

You will collaborate with cross-functional partners to drive program goals, shape future targets, and contribute to publications and data reviews. On-site position with global impact.

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