Clinical Research Coordinator

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. #J-18808-Ljbffr