Pfizer
Healthcare
ClinicalDevelopmentSeniorMedicalDirector,BreastOncology
Neural analysis suggests this role is
optimal for Senior candidates.
“Clinical Development Senior Medical Director, Breast Oncology at Pfizer. Skills: Clinical development, Breast Oncology, Medical monitoring. Conduct medical monitoring activities. Assess eligibility”
What You'll Achieve.
Ensure program meets standards
Industry & Context.
2.5 days per week onsite, Travel several times per year, Permanent work authorization in US
What They're Looking For.
Must Have
Medical degree, 5+ years industry experience, 4+ years clinical oncology experience
Nice to Have
Board certified/eligible in oncology, 2+ years Breast Oncology experience, Late phase clinical development experience, Diverse leadership experiences, Ability to influence and collaborate, Develop and coach others, Oversee and guide colleagues
What You'll Do.
Conduct medical monitoring activities
Lead investigator interactions
Serve as contact for clinical issues
Lead document development
Contribute to document maintenance
Provide clinical development leadership
Serve as Clinical Development Lead
Create development strategies
Refine development strategies
Represent company externally
Serve as committee member
Interpret clinical data
Identify key findings
Identify key implications
Communicate findings to stakeholders
Maintain clinical expertise
Maintain professional competence
Advise on clinical development plans
Drive clinical development plans
How You'll Work.
Team & Collaboration
Cross-functional team; Global Development Team; Study teams; Development subteams
Communication Scope
Peer-to-peer interactions; External engagements
Full Job Description
**Job Summary** This position is for a Clinical Development Senior Medical Director within the atirmociclib program. This individual contributor will be responsible for supporting clinical trial(s) and lead sub teams in clinical development. The successful candidate should ideally have prior experience in clinical trials, supporting development programs, health authority interactions and demonstrated leadership capabilities to ensure that the clinical development program meets scientific, ethical, and regulatory standards. **Job Responsibilities** _Clinical Development Leadership on Study Teams and Development Subteams_ * Conduct medical monitoring activities including eligibility assessment, data review and safety monitoring. * Lead peer-to-peer interactions with investigators * 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, in collaboration with Clinical Scientist and the cross-functional team. * Provide clinical development leadership across several study teams. * Serve as the Clinical Development Lead on subteams including for Marketing Authorization Applications. _Strategic Guidance, Clinical Insights & Interpretation_ * Collaborate with the Global Development Team to create and refine development strategies. * Represent the company in external engagements or as committee member in joint collaborations. * Collaborate with Clinical Scientists to review and interpret clinical data, identify key findings and implications, and communicate to internal and external stakeholders. * Maintain a high level of clinical expertise and professional competence by staying abreast of the latest developments, literature, and guidelines to advise on and drive current and future clinical development plans. **Basic Qualifications** * Medical degree with 5+ years of industry expe
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