Title: Sr Research Associate I (Contractor, Nonclinical Safety)
Location: Foster City, CA
Duration: 12 Months on W2
Specific Responsibilities:
Coordinator for high throughput early discovery assays, following template work instructions.
Work collaboratively with internal research departments and multi-site CROs to ensure data and reports are received and uploaded to databases in a timely manner to inform project teams of safety liabilities
Provide QC review of nonclinical regulatory documents, data tables, study protocols, and reports.
May assist with administrative tasks including document management.
Knowledge, Experience, and Skills:
2+ years of pharmaceutical or CRO industry experience in small molecule and/or biopharmaceutical drug development
Must have strong attention to detail and quality of work.
Ability to prioritize multiple tasks, plan proactively and meet deadlines.
Must have strong computer skills such as Word, PowerPoint, and Excel.
BS or BA degree in a scientific discipline.
1+ years of pharmaceutical or CRO industry experience in small molecule and/or biopharmaceutical drug development
Knowledge of the general principles and methods of toxicology, animal and human biology, and physiology is required.
