Preclinical Study Coordinator: GLP & Collaboration

inotivco; Boulder (CO); On-site; USD 36,000 - 43,000; Full time

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 is seeking a Study Coordinator in Boulder, CO to support the full preclinical study process. You will interact with study directors, technicians, vendors, and clients to ensure materials are prepared, data sheets are created, and study activities are scheduled efficiently.

The role emphasizes strict adherence to GLPs and AAALAC guidelines, meticulous data handling, and timely training documentation. Compensation ranges from $26 to $31 per hour, with competitive benefits and career growth

Qualifications

• Bachelor's degree in life sciences or related field with 3 years in a pharmaceutical setting.
• One year animal handling experience is required.
• Excellent editing for draft protocols, spreadsheets, and reports.
• Experience using Word, Excel, and Outlook.
• Excellent written and verbal communication skills.
• Attention to quality, detail, and following written instructions.
• Ability to interact with scientific staff at all levels.

Responsibilities

• Maintain and submit study initiation materials.
• Communicate with stakeholders including vendors and clients.
• Order supplies for studies and schedule activities with other coordinators.
• Ensure creation of data sheets and review raw data collection forms.
• Support in-life study conduct as trained and approved.
• Complete training and maintain training documentation.
• Review SOPs for accuracy and participate in SOP revisions.
• Maintain compliance with GLPs, USDA, AAALAC, OLAW and other regs.
• Perform quality checks on Inotiv documents and maintain templates.
• Back-up support for Study Directors as needed.
• Prepare archival study files and ensure proper shipment of study samples.

Skills

Bachelor's degree in life sciences

3 years in pharma setting

Animal handling experience

Editing protocols and reports

Microsoft Office proficiency

Strong written and verbal comms

Attention to detail

Ability to work with scientific staff

Education

Bachelor's degree in life sciences or related field

Tools

Microsoft Office

Job description

Inotiv is seeking a Study Coordinator in Boulder, CO to support the full preclinical study process. You will interact with study directors, technicians, vendors, and clients to ensure materials are prepared, data sheets are created, and study activities are scheduled efficiently.

The role emphasizes strict adherence to GLPs and AAALAC guidelines, meticulous data handling, and timely training documentation. Compensation ranges from $26 to $31 per hour, with competitive benefits and career growth