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Regeneron

Senior Medical Director, Clinical Development, CV/Renal/Metabolism

Regeneron

. Serve as Scientific and Medical Lead for clinical teams .

Posted 10/14/2026full-timeUnited StatesSenior💰 $333,300 - $450,900 per yearWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in clinical development strategy, regulatory submissions, and patient safety, with a strong focus on protocol design and execution. Proven ability to lead clinical teams and collaborate effectively with cross-functional partners to drive innovative clinical strategies.

Highest-signal resume keywords
MD Or Equivalent Advanced Medical DegreeClinical Development ExperienceProtocol DesignRegulatory FilingsInternal Medicine Clinical Training

ATS Keywords

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Applicant Tracking System Keywords

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

Hard Skills
Clinical Development StrategyRegulatory SubmissionsPhase 2/3 Program DesignPhase 1 Clinical Testing PlansSignal DetectionClinical Document Quality AssuranceStudy Start-UpHealth Authority InteractionsPatient Safety SafeguardingClinical Communication Strategy
Soft Skills
CollaborationLeadershipCommunication
Certifications & Qualifications
Board Certified Or Eligible In Internal Medicine, Endocrinology, Or Cardiology
Industry Keywords
Clinical TrialsPost-Marketing SurveillanceClinical StudiesInvestigator BrochuresStudy ReportsExternal Stakeholder InteractionsKey External Presentations

About the role

Key responsibilities & impact
  • Serve as Scientific and Medical Lead for clinical teams
  • Guide clinical development strategy and regulatory submissions
  • Collaborate with Operational Leads, discovery teams, and Global Patient Safety
  • Develop innovative clinical strategies to shorten development cycles
  • Design efficient, robust Phase 2/3 programs
  • Partner with discovery teams to inform next-generation targets
  • Lead Phase 1 clinical testing plans for initial PK/PD and safety characterization
  • Safeguard patient safety in clinical studies
  • Support signal detection from post-marketing surveillance
  • Act as medical expert and leader in interactions with external stakeholders
  • Plan and execute publication and clinical communication strategy
  • Contribute to key external presentations
  • Ensure the quality of clinical documents, including investigator brochures, protocols, study reports, and regulatory submission materials
  • Report to an Executive Medical Director, Internal Medicine

Requirements

What you’ll need
  • MD or equivalent advanced medical degree
  • Clinical training in Internal Medicine, Endocrinology, or Cardiology (board certified or eligible strongly preferred)
  • Minimum of 4+ years of clinical development experience in industry
  • Experience with protocol design, study start-up, and study team execution
  • Experience with regulatory filings and health authority interactions preferred
  • Willingness to travel 10% to relevant conferences

Benefits

Comp & perks
  • Annual bonuses or other incentive plans
  • Equity awards
  • Pension or retirement benefits
  • 401(k) company match
  • Health and wellness programs
  • Fitness centers
  • Medical, dental, vision, life, and disability insurance benefits
  • Paid time off
  • Family support benefits
  • Reasonable accommodation during the recruitment process where required