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MSD

Associate Vice President, Global Clinical Development, Oncology Assets

MSD

Associate Vice President managing clinical research activities for oncology indications, leading cross-functional teams and overseeing study cycles.

Posted 5/19/2026full-timeRahway • California, New Jersey, Pennsylvania • 🇺🇸 United StatesJuniorMid-Level💰 $342,800 - $539,600 per yearWebsite

About the role

Key responsibilities & impact
  • planning and directing clinical research activities involving new or marketed drugs for oncology indications
  • manage and oversee the entire cycle of clinical development, including study design, initiation, execution, monitoring, analysis, regulatory reporting, publication, and presentation
  • evaluating pre-clinical and translational work for the purpose of generating early clinical development plan and Investigational New Drug applications
  • developing clinical development strategies for investigational or marketed vaccines
  • monitoring and managing the conduct of ongoing or new clinical trials for investigational or marketed vaccines
  • analyzing and summarizing the clinical findings from studies
  • participation in internal and joint internal/external research project teams relevant to the development of new compounds,
  • mentoring and career development for direct reports

Requirements

What you’ll need
  • M.D or M.D./Ph.D.
  • Board certified or board eligible in medical oncology, radiation oncology, surgical oncology or related disciplines preferred
  • Minimum of 10 years of industry experience in drug development or biomedical research experience in academia or an equivalent combination of academic and industry experience
  • Minimum of 3 years of clinical medicine experience
  • Understanding of full E2E drug development process and ideally candidate would have in-depth experience in early and/or late development
  • Has demonstrated success in running multiple studies and protocols
  • Good evidence of an ability to devise and implement strategic initiatives across functional groups and global pharma teams
  • Demonstrated experience in the design, implementation, and analysis of clinical trials
  • Strong interpersonal skills

Benefits

Comp & perks
  • medical, dental, vision healthcare and other insurance benefits (for employee and family)
  • retirement benefits, including 401(k)
  • paid holidays, vacation, and compassionate and sick days

ATS Keywords

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Hard Skills & Tools
clinical researchstudy designclinical developmentregulatory reportingclinical trialsdata analysisInvestigational New Drug applicationsclinical findings analysisstrategic initiatives implementationprotocol design
Soft Skills
mentoringcareer developmentinterpersonal skillsleadershipcommunication
Certifications
M.D.M.D./Ph.D.board certified in medical oncologyboard certified in radiation oncologyboard certified in surgical oncology