To discuss more about this job opportunity, please reach out to Chitrank Rastogi (LinkedIn URL - https://www.linkedin.com/in/chitrank-rastogi-55119a102/), email your updated resume at Email - chitrank.rastogi@collabera.com or give me a call at (425) 523-1648. Thank you!

Pay Range - $35 to $38/hr. (negotiable)

Job Description:
Job Roles & Responsibilities:

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 a scientific discipline.