Nonclinical Research Associate I – Study Coordination & Data

Charles River Laboratories; Ashland (OH); On-site; USD 28,000 - 40,000; Full time

Job summary

Charles River Laboratories is seeking a supervisor to oversee study-related activities for nonclinical studies. You will coordinate scheduling, review protocols, and ensure data is collected and organized in line with SOPs and study plans.

The role requires a minimum of 2 years in a GLP environment, along with a high school diploma or GED. You must be able to organize, prioritize, and work in the United States without visa sponsorship. The pay is $25.00/hr, with location in Ohio.

Qualifications

• Education: High School diploma or General Education Degree (G.E.D.) preferred.
• Experience: 2 years of related experience in a GLP environment.
• An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
• Certification/Licensure: None
• Other: Ability to organize, prioritize work and meet deadlines. Computer literacy with word processing, spreadsheet, and data base programs.
• Must be authorized to work in United States without a sponsor visa now or in the future.

Responsibilities

• Coordinates assignments to facilitate scheduling of study-related events on assigned studies (in conjunction with other departments) to ensure protocol requirements are met.
• Review study protocols and provide recommendations to study director/supervisor on technical and logistical aspects of protocol design.
• Assist in preparing responses to both internal and external quality assurance audits.
• Responsible for the accurate preparation and review of study calendars from draft and final protocols and ensuring all protocol-driven activities are accurately scheduled.
• Monitors scientific projects, and the conduct of procedures in accordance with the study protocol, and applicable SOP's.
• Acts as liaison between technical staff, internal departments, and Study Director on assigned studies.
• May perform limited technical activities as needed.
• Coordinate ordering of study equipment and supplies.

Skills

Organize work

Prioritize tasks

Computer skills

Education

High School diploma or GED

Job description

Charles River Laboratories is seeking a supervisor to oversee study-related activities for nonclinical studies. You will coordinate scheduling, review protocols, and ensure data is collected and organized in line with SOPs and study plans.

The role requires a minimum of 2 years in a GLP environment, along with a high school diploma or GED. You must be able to organize, prioritize, and work in the United States without visa sponsorship. The pay is $25.00/hr, with location in Ohio.