Apply

Ready to go for it?

AI Apply speeds things up—apply directly if you prefer.

FREE ACCESS
5,000–10,000 jobs/day
JobTailor Logo

See all jobs on JobTailor

Search thousands of fresh jobs every day.

Discover
  • Fresh listings
  • Fast filters
  • No subscription required
Create a free account and start exploring right away.
Regeneron

Senior Medical Director, Clinical Development, Cardiovascular/Metabolism

Regeneron

Senior Medical Director leading clinical development strategies for Cardiovascular/Renal/Metabolism portfolio. Engaging with external stakeholders and ensuring quality clinical documentation.

Posted 5/17/2026full-timeTarrytown • New Jersey, New York • 🇺🇸 United StatesSenior💰 $333,300 - $450,900 per yearWebsite

About the role

Key responsibilities & impact
  • Acts as medical expert and leader in interactions with external stakeholders
  • Develops unique and innovative clinical strategies to significantly shorten the development cycle in the face of an evolving regulatory landscape.
  • Designs and develops more efficient and innovative, yet robust Phase 2/3 programs.
  • Works closely with discovery teams to provide input on the next generation of targets in the field and leads the development of plans for Phase 1 clinical testing for initial characterization of the molecules PK/PD and safety.
  • Ensures safety of the drug, including the safety aspects of patients in clinical studies and signal detection from post-marketing surveillance, with the support from Global Patient Safety.
  • Plans and executes publication and clinical communication strategy in coordination with Publications team.
  • Provides input to key external presentations.
  • Ensures quality of all clinical documents (e.g., Investigators’ Brochure, protocol, study report, clinical components of regulatory submissions, safety related documents).
  • Develops written responses to regulatory agency questions and regulatory submission documents.

Requirements

What you’ll need
  • A minimum of an advanced degree in medicine (i.e., M.D. or D.O. or equivalent)
  • Clinical training in Endocrinology or Cardiology (board certified or eligible or equivalent) is strongly preferred
  • A minimum of 4 years of relevant clinical development experience in industry leading clinical trials including: protocol design, managing study start-up, directing and guiding study team execution, data cleaning, medical monitoring/review, database locks
  • Experience with regulatory filings and interactions with health authorities preferred

Benefits

Comp & perks
  • health and wellness programs (including medical, dental, vision, life, and disability insurance)
  • fitness centers
  • 401(k) company match
  • family support benefits
  • equity awards
  • annual bonuses
  • paid time off
  • paid leaves (e.g., military and parental leave) for eligible employees at all levels!

ATS Keywords

✓ Tailor your resume
Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills & Tools
clinical strategiesPhase 2/3 programsPhase 1 clinical testingPK/PDsafety signal detectionclinical documents qualityregulatory submission documentsprotocol designdata cleaningmedical monitoring
Soft Skills
leadershipcommunicationcollaborationstrategic planninginnovation
Certifications
M.D.D.O.board certified in Endocrinologyboard certified in Cardiology