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USA - Medical Director - III - USD (contract)
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Pfizer
San Diego, CA (In Person)
Full-Time
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Job Description
USA
- Medical Director
- III•USD (contract) Pfizer•4.
- $144 an hour 23 hours ago Benefits Commuter assistance Disability insurance Health insurance Dental insurance 401(k) Vision insurance Life insurance Qualifications Doctor of Medicine Medicine Research ethical considerations Patient safety Doctor of Pharmacy Clinical program data analysis Compliance documentation Managing clinical research teams Oncology research Pharmacy Biomedical regulatory compliance Communication with regulatory authorities for clinical trials Clinical team leadership Oncology Senior level Cross-functional collaboration Clinical data analysis Clinical trial support in drug product development Cross-functional team management Leadership 2 years Project stakeholder communication Cross-functional communication Leading research teams
Full Job Description Summary:
The medical director provides Clinical Development leadership and expertise on clinical trials, including overseeing the design, conduct, and analysis. The medical director works closely with other functions such as regulatory affairs, pharmacovigilance, biostatistics, and medical affairs to ensure that the clinical development program meets the scientific, ethical, and regulatory standards. The medical director also provides medical expertise and guidance to the clinical operations team, the investigators, and the external stakeholders such as health authorities, ethics committees, and patient advocacy groups.Job Responsibilities:
Study-level Clinical Development Leadership. Collaborate with Clinical Scientist(s) to provide clinical leadership across 2-3 study teams that is scientifically rigorous and aligns with company objectives. 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. Strategic Guidance, Clinical Insights & Interpretation. Collaborate with Clinical Scientist to review and interpret clinical data, identify key findings and implications, and communicate to internal and external stakeholders. Maintains 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.Job Qualifications:
Medical degree. Healthcare background (PharmD, NP etc.) with relevant clinical or industry experience considered (typically 4+ years). 2-5 years industry experience. Board certified/eligible in oncology or equivalent preferred. Pay Rate Range 139- 144 USD hourly Additional Notes Please note that contractors are engaged to provide services to Pfizer on a temporary basis in connection with a specific assignment.