Merieux NutriSciences
Clinical Research Coordinator
Merieux NutriSciences, Addison, Illinois, United States, 60114
Clinical Research CoordinatorAddisonRegularMERIEUX NUTRISCIENCESAs 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 LIFEWe 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.At any time, the incumbent must behave and operate in an ethical and Code of Conduct compliant manner
.Communication:Internal Interlocutors: Internal Clinic & OperationsExternal Interlocutors: ClientsYOUR PROFILEProfile:* 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:* NoneWork 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.#LI-DNPWHY 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.
Ready for the journey?To apply please click on 'Apply now' button
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 LIFEWe 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.At any time, the incumbent must behave and operate in an ethical and Code of Conduct compliant manner
.Communication:Internal Interlocutors: Internal Clinic & OperationsExternal Interlocutors: ClientsYOUR PROFILEProfile:* 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:* NoneWork 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.#LI-DNPWHY 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.
Ready for the journey?To apply please click on 'Apply now' button