Clinical Research Coordinator

Merieux NutriSciences; Addison (IL); On-site; USD 60,000 - 65,000; Full time

Benefits offered by this job

Medical insurance

PTO

401(k)

Job summary

Merieux NutriSciences in Addison, IL is seeking a Clinical Research Coordinator to manage day-to-day clinical study activities, including participant recruitment, consent, data collection and protocol adherence.

The role reports to Clinical Site Manager and involves collaboration with sponsors, IRBs and staff; requires at least 2 years in clinical/public health, CPR cert, and potentially nursing or dietitian licensure; office-based with occasional travel; salary $60k–$65k USD.

Qualifications

• Requires at least 2 years of experience in clinical processes/public health or a degree in biology, pharmacology or related field.
• CPR certification is necessary.
• Registered Nurse, Registered Dietitian, or Licensed Practical Nurse certification is preferred.

Responsibilities

• Recruit, screen and enroll clinical study participants.
• Obtain proper written informed consent from each 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.

Skills

Organizational skills

Written communication

Verbal communication

Education

Biology/Pharmacology degree

Job description

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.

Management

• None

Work Environment

The position primarily works in an office environment in which surroundings are usually comfortable. The usual work hours are 40 hours a week. Some work projects may require the position to work extended hours. Little travel is required. Physical dexterity is necessary to effectively manipulate a keyboard. The incumbent can expect extended time spent in a sitting position. Periodically, the position may lift heavy boxes (up to 25 pounds) such as accounting records.

Compensation and Benefits

• Compensation Range: $60,000 - $65,000 annual salary USD
• Full Time
• Comprehensive medical, dental, and vision insurance plans.
• Generous paid time off (PTO) package to support work-life balance following state and local ordinances.
• Optional 401(k) plan with employer matching contributions.

The information above provides a general overview and may vary based on specific job responsibilities, location, or other factors. Details will be clarified during the hiring process.