BCBA delivering clinical - behavioral assessments and support plans for adults with disabilities at Vinfen. Collaborating with multidisciplinary teams to enhance clients' quality of life.
PF
Hybrid Associate Director, Clinical Development – Medical Director, MD
Posted 5 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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