Clinical Research Coordinator

Mérieux NutriSciences Dietary Supplement Testing North America; Addison (IL); On-site; USD 60,000 - 65,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

Paid time off

401(k) matching

Job summary

MERIEUX NUTRISCIENCES is seeking a Clinical Research Coordinator in Addison, IL to oversee operational responsibilities for dietary and clinical studies under the Clinical Site Manager.

The role requires at least 2 years in clinical processes or public health, CPR certification, and prefers RN/RD/LPN credentials.

Qualifications

• Minimum 2 years of experience in clinical processes/public health.
• CPR certification is required.
• 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 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.

Skills

Organizational skills

Written communication

Verbal communication

Education

Biology or Pharmacology degree

Job description

MERIEUX NUTRISCIENCES

Addison

Regular (US Only)

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

Purpose (Objective)

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

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

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 Package Overview

• Compensation Range $60,000 - $65,000 annual salary USD

Full Time Eligible Benefits Overview

• 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.

WHY JOIN US

• Because you would contribute to an inspiring Public Health purpose, supported by long-term and visionary shareholders.


• Because you would have an impact on our strategic pillars that build on 50 years of experience and expertise.


• Because you would be part of a community of an enthusiastic and skilled group of people who love co-building together and serving a purpose bigger than them.


• Because you would be welcome as you are, in a diverse and open-minded environment that is rich in our singularities and differences.


• Because you would grow in an international group of more than 8200 fantastic team members, with plenty of opportunities to learn and share.