Senior Study Coordinator - Life Sciences Lab

Inotiv, Inc.

Westminster (CO)

On-site

USD 54,000 - 69,000

Full time

12 days ago
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Benefits offered by this job

Health and dental coverage
Short- and long-term disability
Paid time off
Paid parental leave
401(k) and more

Job summary

Inotiv, Inc. in Westminster, CO, is seeking a Study Coordinator to support life science studies.

You will manage initiation materials, schedule activities with other coordinators, and ensure data sheets and protocols are created and followed according to SOPs. Responsibilities include maintaining training records, performing quality checks on documents, and assisting study directors as needed while upholding USDA/OLAW/GLP standards.

Qualifications

  • Bachelor's degree in life sciences or related field.
  • Minimum three years in a relevant pharmaceutical setting.
  • At least one year of experience with animals and animal handling.
  • Good knowledge of general laboratory procedures and CFR requirements.

Responsibilities

  • Maintain and submit study initiation materials.
  • Order all applicable supplies for studies.
  • Coordinate with other coordinators to schedule study activities.
  • Ensure creation of data sheets and adherence to protocol.
  • Perform data quality checks and review for protocol compliance.
  • Provide back-up support for Study Directors as needed.
  • Maintain training documentation and SOP compliance.

Skills

Laboratory procedures
Customer-focused
Communication
CFR compliance
Word/Outlook/Excel
Editing data and reports
Attention to detail
Team collaboration

Education

Bachelor's degree in life sciences or related field

Tools

Word
Outlook
Excel

Job description

Inotiv, Inc. in Westminster, CO, is seeking a Study Coordinator to support life science studies.

You will manage initiation materials, schedule activities with other coordinators, and ensure data sheets and protocols are created and followed according to SOPs. Responsibilities include maintaining training records, performing quality checks on documents, and assisting study directors as needed while upholding USDA/OLAW/GLP standards.

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