Director - Clinical Research Scientist
Description:
Collaborate with a therapeutic area VP of Clinical Development, the Clinical Research Scientist will contribute to the design, conduct, analysis, and reporting of clinical trials.
Apply scientific training and clinical research experience to support all aspects of drug development.
Facilitate the transition of molecules from pre-clinical discovery to supporting the registration and commercialization of a product.
Requirements:
Advanced degree in Sciences (e.g.MD or equivalent, PharmD, PhD,) preferred, not required. Advanced masters degree with experience will be considered.
Clinical trial experience in the pharmaceutical industry, academia, or equivalent is preferred. (>2 years of experience as a CRS in pharmaceutical industry required)
Ability to provide input and direction to clinical research with appropriate supervision.
Strong desire to collaborate in a cross-functional setting.
Knowledge of clinical trial methodology, regulatory and compliance requirements governing clinical trials and experience in the design of study protocols.
Benefits:
Equity and other forms of compensation may be provided as part of a total compensation package,
Full range of medical, dental, and vision benefits,
401k,
Unlimited paid time off,
Parental leave.
Apply Now
Collaborate with a therapeutic area VP of Clinical Development, the Clinical Research Scientist will contribute to the design, conduct, analysis, and reporting of clinical trials.
Apply scientific training and clinical research experience to support all aspects of drug development.
Facilitate the transition of molecules from pre-clinical discovery to supporting the registration and commercialization of a product.
Requirements:
Advanced degree in Sciences (e.g.MD or equivalent, PharmD, PhD,) preferred, not required. Advanced masters degree with experience will be considered.
Clinical trial experience in the pharmaceutical industry, academia, or equivalent is preferred. (>2 years of experience as a CRS in pharmaceutical industry required)
Ability to provide input and direction to clinical research with appropriate supervision.
Strong desire to collaborate in a cross-functional setting.
Knowledge of clinical trial methodology, regulatory and compliance requirements governing clinical trials and experience in the design of study protocols.
Benefits:
Equity and other forms of compensation may be provided as part of a total compensation package,
Full range of medical, dental, and vision benefits,
401k,
Unlimited paid time off,
Parental leave.
Apply Now