Senior Medical Director leading clinical trials in breast oncology development. Collaborating with global teams and overseeing clinical monitoring and regulatory documentation.
Responsibilities
Responsible for supporting clinical trial(s) and lead subteams in clinical development
Conduct medical monitoring activities including eligibility assessment, data review and safety monitoring
Lead peer-to-peer interactions with investigator
Serve as the point of contact for clinical issues between the study team, investigators, ethics committees, steering committees, and regulatory authorities
Lead and contribute to development and maintenance of clinical trial and regulatory documents
Oversees and provides clinical development leadership across several study teams
Collaborates with the Global Development Team to create and refine development strategies
Represents the company in external engagements or in committee members
Requirements
Medical degree required
5+ years industry experience in Clinical Development
Experience Leading late phase clinical trials in Oncology
Experience in medical monitoring, disease area strategy and data cleaning
Board certified/eligible in oncology or equivalent preferred
Breast oncology experience preferred
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 and an 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
Comprehensive and generous benefits and programs to help our colleagues lead healthy lives
Job title
Senior Medical Director, Clinical Development – Breast Oncology
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