Sr Research Associate
4 weeks ago
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.
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