AS
Senior Medical Director providing medical and scientific input for early phase clinical development in Rheumatology. Collaborating with cross - functional teams and external partners to deliver innovative clinical studies.
About the role
- Accountable for medical & scientific integrity of the study and patient wellbeing
- Apply technical and clinical/medical skills for efficient trial design and execution
- Execute studies in partnership with clinical and medical colleagues
- Provide medical monitoring for clinical trials and manage protocol deviations
- Contribute to development of protocol design documents and amendments
- Ensure compliance with internal and external standards
Requirements
- Obtained a primary medical degree (e.g., MD, DO, MBBS, MBChB)
- Minimum of 4-years Clinical Development experience in industry/CRO
- Licensed to prescribe medicines independent of supervision for at least 2 years post-internship
- Maintained registration/Medical License to practice in good standing
- Clinical research experience in phase 3/pivotal space
- Demonstrated scientific writing skills and scientific productivity via publications, posters, abstracts, presentations
- 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
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 including medical, prescription drug, dental and vision coverage
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