Global Medical Affairs Director at ViiV Healthcare ensuring effective communication of HIV prevention research. Leading training and data compliance efforts for clinical specialists and outside health care providers.
PF
Hybrid Associate Director, Clinical Development – Medical Director, MD
Posted 3 months ago
About the role
- Medical Director accountable for clinical trial integrity and patient wellbeing at Pfizer. Collaborating on protocol design and ensuring compliance while managing clinical data review.
Responsibilities
- 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
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