GLP Study Coordinator - Research Associate I

RXinsider LTD.; Ashland (OH); On-site; USD 30,000 - 39,000; Full time

Job summary

Charles River is seeking a supervisor to coordinate study-related activities in a GLP environment. You will oversee technical staff, manage study calendars, and ensure protocol adherence while maintaining data quality and timely submissions.

The role involves liaising with internal teams and the Study Director, supporting audits, and contributing to continuous process improvements in preclinical studies.

Qualifications

• Education: High School diploma or GED preferred.
• Experience: 2 years in a GLP environment.
• Equivalent combinations of education and experience acceptable.
• No certification/licensure required.
• Ability to organize, prioritize work and meet deadlines.
• Authorized to work in the United States without visa sponsorship.

Responsibilities

• Coordinate study-related activities to meet protocol requirements.
• Maintain study calendars and data; supervise technical staff.
• Review study protocols and advise on design and logistics.
• Prepare responses for audits and QA reviews.
• Liaise between staff and Study Director on assigned studies.
• Prepare and submit study notebooks to QA and ensure data accuracy.

Skills

Organizational skills

Data handling

Education

High School diploma or GED

Tools

MS Office (Word, Excel, Access)

Job description

Charles River is seeking a supervisor to coordinate study-related activities in a GLP environment. You will oversee technical staff, manage study calendars, and ensure protocol adherence while maintaining data quality and timely submissions.

The role involves liaising with internal teams and the Study Director, supporting audits, and contributing to continuous process improvements in preclinical studies.