Job Description:

A leading Biopharma company are actively seeking a motivated candidate to fill their Sr Nonclinical Safety Research Associate I opportunity. This is an initial 12-month hybrid contract with 3-days on site Foster City and 2-days remote. Salary ranges between $40-45/hour depending on experience.

In this role, you’ll gain extensive knowledge as Study monitor for nonclinical toxicology studies conducted at CROs and responsible for the technical and scientific conduct of studies.

Requirements:

• B.Sc., in scientific discipline with 2 years of pharmaceutical or CRO industry experience in small molecule and/or biopharmaceutical drug development.

• Or M.Sc., degree with 4 years’ experience.

• Ability to prioritize multiple tasks, plan proactively, and meet deadlines.

• Must have strong computer skills such as Word, PowerPoint, and Excel.

Responsibilities:

• Coordinator for high throughput early discovery assays, following templated 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 on safety liabilities

• Provide QC review of nonclinical regulatory documents, data tables, study protocols and reports.