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Senior Research Assistant
3 months ago
Net2Source Inc. is an award-winning total workforce solutions company recognized by Staffing Industry Analysts for our accelerated growth of 300% in the last 3 years with over 5500+ employees globally, with over 30+ locations in the US and global operations in 32 countries. We believe in providing staffing solutions to address the current talent gap – Right Talent – Right Time – Right Place – Right Price and acting as a Career Coach to our consultants.
Job Title: Contractor, Nonclinical Safety
Job Location: Foster City, CA 94404
Hybrid - 3 days onsite and 2 days remote
Job Duration: 12 Months Contract
Job Description:
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.
Unique Selling Point of this role:
Gaining meaningful work experience working at a company with a corporate culture committed to science and patients, and an employee environment that fosters innovation, diversity and a commitment to the personal and professional development of all. Gaining extensive knowledge as Study monitor for nonclinical toxicology studies conducted at CROs and responsible for the technical and scientific conduct of studies.
Required Degree or Certification: BS or BA degree in scientific discipline.
