Non clinical Research Assistant

Title: Non clinical Research Assistant

Location: Foster City, CA- Hybrid

Duration: 12 Months on W2

Specific 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.

• 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 scientific discipline.

Required Years of Experience:

1+ years of pharmaceutical or CRO industry experience in small molecule and/or biopharmaceutical drug development

Top 3 Required Skill Sets:

1+ years of pharmaceutical or CRO industry experience in small molecule and/or biopharmaceutical drug development

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

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

Top 3 Nice to Have Skill Sets:

BS or MS degree in related scientific discipline with 3+ (MS) or 5+ (BS) 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.