Iterative Health
Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 70+ clinical research sites across US and Europe accelerating the path to market for gastrointestinal (GI) and hepatology novel therapies. Our focus is on driving the success and growth of our partner sites by empowering them with tech‑enabled services. By combining deep expertise in clinical trials with cutting‑edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.
We are seeking a full‑time, experienced Clinical Research Coordinator – Registered Nurse (CRC‑RN). The CRC‑RN supports, facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study.
Responsibilities
Administratively and clinically manage industry‑sponsored clinical trials including problem solving, communication and protocol management.
Assist in patient recruitment by performing chart reviews, discussing protocols with patients, and verifying the informed consent documentation to meet enrollment targets on assigned studies.
Schedule all patient research visits and procedures consistent with protocol requirements.
Conduct patient visits as outlined within each study protocol.
Dispense study medication, collect vital signs and perform ECGs.
Administer IV medications, monitor IV tubing, give intramuscular and subcutaneous injections, perform phlebotomy as needed, and monitor patients during infusion and discharge as policies indicate.
Perform blood draws, process and ship specimens per study protocol and IATA regulations.
Enter relevant study and subject specific information into the CTMS system regularly; complete and maintain study files including consent forms, source documentation, progress notes, case report forms, and investigational accountability forms.
Act as point of contact for study participants.
Adhere to Research SOPs, Good Clinical Practices, and the study protocols.
Maintain ongoing communication with the CRO, sponsor, research participants, Site Manager and PI throughout the study.
Ensure all safety data is reviewed by the PI in a timely manner.
Maintain inventory of study equipment and supplies onsite at all times.
Participate actively in communication of status and results to management; contribute and implement ideas to improve site performance.
Assist with routine data verification and quality control, ensuring data integrity and consistency with prescribed study protocol. Meet requirements for data query resolution times and quality.
Schedule and prepare for monitor visits.
Assist Study Team in protection of the rights and welfare of all human research participants in accordance with federal regulations.
Cooperate with site compliance and monitoring efforts regarding the access, use, and disclosure of PHI and report instances of noncompliance.
Complete and maintain case report forms per FDA guidelines, and review them against the patient’s medical record for completeness and accuracy.
All Employees Are Expected To
Perform quality work within deadlines with or without direct supervision.
Interact professionally with other employees, customers and suppliers.
Work effectively as a team contributor on all assignments.
Work independently while understanding the necessity for communicating and coordinating work efforts with other employees and organizations.
Qualifications
Registered Nurse.
Solid nursing background, concentration, or willingness to obtain advanced knowledge in GI specialty.
2-3 years of clinical research experience preferred.
Strong written and verbal communication skills.
Ability to read, interpret, and apply clinical policies and research protocols.
Ability to use standard office software.
Must be able to lift up to 25 pounds.
Diversity Statement At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact
CandidateAccommodations@iterative.health .
Equal Employment Opportunity As set forth in Iterative Health’s Equal Employment Opportunity policy, we do not discriminate on the basis of any protected group status under any applicable law. We strive to provide an inclusive environment for all employees and applicants.
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We are seeking a full‑time, experienced Clinical Research Coordinator – Registered Nurse (CRC‑RN). The CRC‑RN supports, facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study.
Responsibilities
Administratively and clinically manage industry‑sponsored clinical trials including problem solving, communication and protocol management.
Assist in patient recruitment by performing chart reviews, discussing protocols with patients, and verifying the informed consent documentation to meet enrollment targets on assigned studies.
Schedule all patient research visits and procedures consistent with protocol requirements.
Conduct patient visits as outlined within each study protocol.
Dispense study medication, collect vital signs and perform ECGs.
Administer IV medications, monitor IV tubing, give intramuscular and subcutaneous injections, perform phlebotomy as needed, and monitor patients during infusion and discharge as policies indicate.
Perform blood draws, process and ship specimens per study protocol and IATA regulations.
Enter relevant study and subject specific information into the CTMS system regularly; complete and maintain study files including consent forms, source documentation, progress notes, case report forms, and investigational accountability forms.
Act as point of contact for study participants.
Adhere to Research SOPs, Good Clinical Practices, and the study protocols.
Maintain ongoing communication with the CRO, sponsor, research participants, Site Manager and PI throughout the study.
Ensure all safety data is reviewed by the PI in a timely manner.
Maintain inventory of study equipment and supplies onsite at all times.
Participate actively in communication of status and results to management; contribute and implement ideas to improve site performance.
Assist with routine data verification and quality control, ensuring data integrity and consistency with prescribed study protocol. Meet requirements for data query resolution times and quality.
Schedule and prepare for monitor visits.
Assist Study Team in protection of the rights and welfare of all human research participants in accordance with federal regulations.
Cooperate with site compliance and monitoring efforts regarding the access, use, and disclosure of PHI and report instances of noncompliance.
Complete and maintain case report forms per FDA guidelines, and review them against the patient’s medical record for completeness and accuracy.
All Employees Are Expected To
Perform quality work within deadlines with or without direct supervision.
Interact professionally with other employees, customers and suppliers.
Work effectively as a team contributor on all assignments.
Work independently while understanding the necessity for communicating and coordinating work efforts with other employees and organizations.
Qualifications
Registered Nurse.
Solid nursing background, concentration, or willingness to obtain advanced knowledge in GI specialty.
2-3 years of clinical research experience preferred.
Strong written and verbal communication skills.
Ability to read, interpret, and apply clinical policies and research protocols.
Ability to use standard office software.
Must be able to lift up to 25 pounds.
Diversity Statement At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact
CandidateAccommodations@iterative.health .
Equal Employment Opportunity As set forth in Iterative Health’s Equal Employment Opportunity policy, we do not discriminate on the basis of any protected group status under any applicable law. We strive to provide an inclusive environment for all employees and applicants.
#J-18808-Ljbffr