Location: Hybrid 3 days onsite and 2 days remote

Job Title: Contractor, Nonclinical Safety

Contract Length: 12 months

Pay Rate: $45-$48 per hour based on experience

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.
• Required Degree or Certification: BS or BA degree in scientific discipline.