Clinical Research Associate I: Site Coordination & Study Support

biofiredx; Hazelwood (MO); Hybrid; USD 67,000 - 100,000; Full time

Benefits offered by this job

Medical/dental/vision benefits

Retirement plan

Commuter benefits

Wellness programs

Job summary

bioMérieux seeks a Clinical Research Associate I to partner with Clinical Trial Managers, serving as the primary liaison with clinical sites for logistics and issue resolution. You will help ensure regulatory compliance and adherence to study protocols across multiple trials.

The role includes site monitoring, data queries, specimen logistics, and regulatory support, with occasional travel and collaboration across teams.

Qualifications

• Bachelor's degree in Microbiology, Molecular Biology, Life Sciences, Biomedical, or related field.
• No previous experience required.
• Experience with clinical study monitoring preferred.
• 2+ years hands-on immunology, microbiology, or molecular biology lab experience preferred.
• Experience with human subjects testing/research a plus.
• Ability to independently manage projects, identify risks, and report progress.

Responsibilities

• Coordinate with Clinical Trial Managers for site coordination and monitoring.
• Communicate with clinical study sites to ensure protocol compliance and testing adherence.
• Coordinate shipping/receiving of specimens to labs or reference labs as needed.
• Resolve data discrepancies with Data Management and initiate queries.
• Provide logistical, technical, and regulatory support to study personnel.
• Contribute to study procedures and final study reports.

Skills

Regulatory awareness

Communication

Cross-functional collaboration

MS Office

Documentation

Time management

Critical thinking

Biology knowledge

Education

Bachelor's degree in Microbiology/Molecular Biology/Life Sciences

Tools

MS Office (Outlook/Word/Excel)

Job description

bioMérieux seeks a Clinical Research Associate I to partner with Clinical Trial Managers, serving as the primary liaison with clinical sites for logistics and issue resolution. You will help ensure regulatory compliance and adherence to study protocols across multiple trials.

The role includes site monitoring, data queries, specimen logistics, and regulatory support, with occasional travel and collaboration across teams.