Clinical Research Coordinator

Mérieux NutriSciences

United Statesfull_timeVerifiedPosted 15 Jul 2026

💰 $65,000/yr($60,000/yr – $65,000/yr)

About the role

Clinical Research Coordinator

Addison

Regular (US Only)

MERIEUX NUTRISCIENCES

As a trusted partner, our Public Health mission is to make food systems safer, healthier and more sustainable. Throughout our global network in 27 countries, we offer to our customers a wide range of testing and innovative solutions dedicated to preventing health risks related to food, environment and consumer goods. External growth has been a key pillar of our history with more than 40 acquisitions completed in the last 10 years.

If you want to contribute to an inspiring long-term purpose, to be part of a fast growing company on a high-value market with significant build-up opportunities, and to grow in an entrepreneurial and warm environment, join us!

YOUR DAY TO DAY LIFE

We are looking for a Clinical Research Coordinator in 800 S Rohlwing rd, Addison, IL 60101 USA. Your mission will be to:

Purpose (Objective):

The Clinical Research Coordinator is an essential team member in the conduct of dietary, exercise and pharmaceutical studies. This position acts as a point person for the clinical-study site, overseeing all operational responsibilities for the successful launch, enrollment, maintenance and completion of clinical projects. This position will report to the Clinical Site Manager.

Main activities:

● Recruit, screen and enroll clinical study participants.

● Obtain proper written informed consent from each study participant prior to participation in the study.

● Schedule and complete defined activities of the studies completely and accurately.

● Develop source documents and tools specific to the protocol.

● Accurately complete source documents/case report forms, study medication and product accountability.

● Train and brief current and new staff on all operational policies and procedures of the study, ensuring each person understands his/her role and responsibilities in the study. Ensure that the clinical trial is conducted according to the investigational plan (protocol) and Good Clinical Practices.

● Meet and communicate with the Sponsor and/or their designee regarding the conduct of the study.

● Inform Institutional Review Board and Sponsor as appropriate of relevant adverse events.

● Successfully interact with the clinical research team.

● Maintain a high level of knowledge and understanding of assigned protocols.

● Support the corporate quality and continuous improvement process (TQM).

● Perform other duties as needed.

Communication:

Internal Interlocutors: Internal Clinic & Operations

External Interlocutors: Clients

YOUR PROFILE

Profile:

● This position requires at least 2 years of experience in clinical processes/public health or a degree in biology, pharmacology or related field of study.

● CPR certification is necessary.

● Registered Nurse, Registered Dietitian, or License Practical Nurse certification is preferred.

Required skills:

● Strong organizational skills are required to effectively manage operational activities for clinical projects.

● Strong written and verbal communication skills are necessary to develop source documents, reports, and communicate status of the studies to Sponsors and Institutional Review Board.