Study Coordinator - Non-Clinical CRO

Job overview

The Study Coordinator - Non-Clinical CRO role is onsite in Stilwell, KS. Compensation is not specified. The coordinator supports non-clinical studies alongside Study Directors, Scientists, technical staff, and other study personnel. The role exists to help plan, coordinate, execute, and document studies accurately and efficiently in line with protocols, standard operating procedures, regulatory requirements, and client expectations. It monitors study progress, coordinates resources and personnel, maintains records, and helps address issues that could affect study timelines or quality.

What you'll do

• Coordinate day-to-day activities and scheduling for assigned non-clinical studies
• coordinate study resources, equipment, test systems, materials, and personnel
• monitor progress and communicate delays or conflicts
• conduct or assist with procedures within training and qualifications
• record and verify data and observations
• maintain study records
• assist with study documentation and quality checks
• communicate status and issues
• coordinate and train junior personnel as appropriate
• and escalate significant or unresolved issues.

What we're looking for

Skills & competencies

study coordinator

non-clinical cro

people people

stilwell ks

onsite

study coordination

laboratory research

study documentation

protocols and sops

data quality

test systems

3–4 years preferred

Work arrangement

• Weekend coverage required

Why this role

The role may provide day-to-day coordination, guidance, and training to junior study personnel but does not necessarily have formal supervisory responsibilities. A bachelor's degree in a related scientific field and 3–4 years of relevant experience are preferred; equivalent education, training, and experience may be considered.

About the employer

People People is hiring for this role. Industry: Research and Development in the Social Sciences and Humanities. Sector: 54.