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Job description
Role
The Clinical Development Scientist (Director) leads scientific oversight and manages clinical trials in Internal Medicine, focusing on study execution, data integrity, and quality assurance.
Responsibilities
protocol development
internal and external stakeholder interactions
safety and risk management
site selection
investigator training
data review
and contributing to regulatory documentation and publications
Requirements
PhD, PharmD, or equivalent with 5+ years (PhD), 7+ years (MS), or 8+ years (BA/BS) of clinical research experience in biopharma, with expertise in cardiometabolic diseases preferred.
Skills include strong knowledge of clinical development, GxP, ICH/GCP, regulatory processes, and experience managing clinical teams.
High-value specifics involve early to late-stage clinical studies, safety monitoring, and collaboration with global development teams.
The role may require global travel and is based in a hybrid work setting, with an average of 2.5 days/week onsite.
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Worksite address
lake forest, IL, 60045, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.