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Regeneron

Medical Director, Clinical Development, Hematology Oncology

Regeneron

Medical Director leading clinical development for hematology oncology at Regeneron. Drive clinical strategy and execution across trial phases with cross-functional collaboration in a science-driven organization.

Posted 7/28/2026full-timeTarrytown • New Jersey, New York • 🇺🇸 United StatesLead💰 $280,700 - $379,900 per yearWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in leading clinical strategy and execution across trial phases, with a strong focus on hematologic malignancies. Possesses a medical degree and extensive experience in clinical research and drug development, ensuring compliance with global clinical development standards.

Highest-signal resume keywords
MD Or Equivalent Medical DegreeClinical Residency TrainingHematology Or Oncology Fellowship TrainingClinical Research ExperienceMedical/Scientific Expertise In Hematologic Malignancies

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 Strategy DevelopmentTrial Phase ExecutionSOP Authoring And ReviewingClinical Program RepresentationCross-Functional Collaboration
Soft Skills
LeadershipGuidance And SupportCommunication
Industry Keywords
Clinical ResearchDrug DevelopmentRegulatory InteractionsKey Opinion LeadersAdvisory Boards

About the role

Key responsibilities & impact
  • Lead clinical strategy and deliverables for an assigned section of a clinical program
  • Drive execution across trial phases in partnership with global line functions
  • Guide and support assigned Clinical Scientists and Clinical Operations associates
  • Represent the program in interactions with regulatory authorities, key opinion leaders, and advisory boards
  • Partner cross-functionally with Research, Early Clinical Development, Medical Affairs, Marketing, and HE&OR
  • Contribute to internal decision boards shaping program direction
  • Shape Global Clinical Development standards by authoring or reviewing SOPs
  • Participate in training programs and strategic taskforces that advance clinical development practices

Requirements

What you’ll need
  • MD or equivalent medical degree with clinical Residency training
  • Hematology or Oncology fellowship training strongly preferred
  • More than 2 years of experience in clinical research or drug development (academic or industry), spanning Phases I through IV
  • Medical/scientific expertise in the disease area of the assigned program, hematologic malignancies, preferred

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
  • insurance benefits (e.g. medical, dental, vision, life and disability)
  • paid time off
  • family support benefits