Preclinical Study Coordinator | GLP Compliance & Data

BASI Gaithersburg LLC; Boulder (CO); On-site; USD 55,000 - 90,000; Full time

Benefits offered by this job

Health insurance

Dental coverage

Disability insurance

Paid time off

Parental leave

401(k)

Job summary

Inotiv seeks a Study Coordinator in Boulder to support preclinical study processes and communicate with clients, study directors, and technicians.

You will maintain materials, coordinate activities with vendors, ensure data sheets, and assist in in-life study conduct while adhering to SOPs and GLP standards.

Salary will be commensurate with experience; benefits include health and dental coverage, disability, PTO, parental leave, 401(k), and more.

Qualifications

• Bachelor's degree in life sciences or related field required, with 3+ years in pharma setting.
• Animal handling experience required.
• Strong editing and formatting skills for protocols, spreadsheets, and reports.

Responsibilities

• Maintain and submit study initiation materials.
• Communicate with vendors and clients.
• Order supplies for studies.
• Coordinate study activities with other coordinators.
• Ensure creation of data sheets.
• Review SOPs to ensure accuracy and compliance with GLPs, USDA, AAALAC, OLAW.

Skills

Communication

Attention to detail

Interpersonal skills

Education

Bachelor's degree in life sciences or related field

3+ years in pharmaceutical setting

Animal handling experience

Tools

MS Word

Excel

Outlook

Job description

Inotiv seeks a Study Coordinator in Boulder to support preclinical study processes and communicate with clients, study directors, and technicians.

You will maintain materials, coordinate activities with vendors, ensure data sheets, and assist in in-life study conduct while adhering to SOPs and GLP standards.

Salary will be commensurate with experience; benefits include health and dental coverage, disability, PTO, parental leave, 401(k), and more.