Hybrid Associate Director, Clinical Development – Medical Director, MD

Posted last week

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About the role

  • Is accountable for the medical & scientific integrity of the study and the wellbeing of the patients enrolled in one or more clinical trials
  • Applies technical and clinical/medical skills to ensure the design of efficient and high-quality clinical trials
  • Responsible for effective execution of studies and works in close partnership with other clinical and medical colleagues, clinical operations, and other functional lines
  • Accountable for timely delivery of a quality protocol, clinical execution of clinical trials and supports appropriate interpretation and communication of clinical trial data
  • Maintains compliance with internal and external standards, proactively mitigates risk and manages emerging clinical/medical issues through timely, diligent clinical data, safety and protocol deviation review
  • May perform medical monitoring of one or more clinical trials
  • Will be the primary contact with external investigators & the internal study team for questions relating to clinical/medical aspects of the protocol
  • Partners with/supports the Global Development Lead regarding study and disease area strategy

Requirements

  • Obtained a primary medical degree (e.g., MD, DO, MBBS, MBChB) from a recognized medical school/university
  • Clinical research experience
  • Licensed by a licensing body/health authority to prescribe medicines independent of supervision for at least 2 years post intern/house officer/foundation period
  • Maintained registration/Medical License to practice and always have been in good standing with their Medical Licensing Authority
  • Clinical research experience in phase 3/pivotal space
  • Demonstrated scientific writing skills; scientific productivity via publications, posters, abstracts, and/or presentations
  • Clinical Research experience in industry/CRO preferred
  • Cardiometabolic disease experience highly preferred (ie, cardiology, obesity, endocrinology, nephrology etc.)
  • Extensive knowledge of clinical development, global and regional regulation, ICH/GCP, adverse event management
  • Demonstrated clinical/medical, administrative, and project management capabilities
  • Excellent verbal and written communication skills in English, in relating to individuals both inside and outside Pfizer
  • Candidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact.

Benefits

  • 401(k) plan with Pfizer Matching Contributions
  • Additional Pfizer Retirement Savings Contribution
  • Paid vacation
  • Holiday and personal days
  • Paid caregiver/parental and medical leave
  • Health benefits to include medical, prescription drug, dental, and vision coverage

Job title

Associate Director, Clinical Development – Medical Director, MD

Job type

Experience level

Senior

Salary

$182,000 - $303,300 per year

Degree requirement

Postgraduate Degree

Location requirements

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