About this opportunity
Pfizer lists this USA - Medical Director - III - USD opportunity in san diego, California. Review the employer’s description below for duties, qualifications and application requirements.
Job description
USA - Medical Director - III - USD (Contract)
Contract (6 months)
Published 16 days ago
On hold
Solid Tumor
oncology clinical development
Medical Affairs
medical expertise
clinical trials
Safety monitoring
Health authorities
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
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
Min Pay Rate $139
Max Pay Rate $144
Currency USD
Unit hourly
Benefits Information
Comprehensive Benefits Package available based on eligibility
Short-Term Disability (STD)
Long-Term Disability (LTD)
Supplemental and Voluntary Life Insurance
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Worksite address
san diego, CA, 92189, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.