Iterative Health
Clinical Research Coordinator I - Nurse
Tucson, AZ
Sponsorship not specifiedDetected 4 days ago
GCPHIPAAClinical TrialsClinical ResearchFDA RegulatoryResearchCommunicationProblem SolvingOrganizational SkillsGxP
About the role
- Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes.
- We built a leading performance-driven network of 100+ sites across the US, Europe, India, and Australia, conducting research directly in the communities where care is delivered across gastrointestinal, hepatology, obesity, and cardiology.
- By combining deep clinical trial expertise with cutting-edge AI, we connect sponsors' scientific ambitions with high-performing research teams that expedite and expand access to novel therapeutics for patients in need.
Responsibilities
- Administratively and clinically manage industry-sponsored clinical trials, including problem-solving, communication, and protocol management.
- Complete and maintain study documentation including consent forms, source documentation, progress notes, case report forms, and investigational accountability forms.
- Lead patient recruitment activities including chart reviews, protocol discussions with patients, and verification of informed consent documentation.
- Dispense study medication, collect vital signs, and perform ECGs per protocol.
- Perform blood draws; process and ship specimens per study protocol and IATA regulations.
Nice to have
- Prior GI or hepatology clinical research experience.
- Familiarity with GCP guidelines and FDA regulations governing clinical research.
- Experience with CTMS, EDC, or eTMF platforms.
- ACRP or SOCRA certification (CCRC or CCRP), or active pursuit of certification.
- Adhere to Research SOPs, Good Clinical Practice (GCP) guidelines, and study protocols at all times.
- Assist with routine data verification and quality control, ensuring data integrity and consistency with prescribed study protocols.
- Ensure all safety data is reviewed by the PI in a timely manner.
- Cooperate with site compliance and monitoring efforts regarding the access, use, and disclosure of PHI
Benefits
- Complete and maintain case report forms per FDA guidelines, reviewing them against patient medical records for completeness and accuracy.
Visa & Work Authorization
- Maintain ongoing communication with the CRO, sponsor, research participants, Site Manager, and PI throughout the course of each study
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This listing is sourced directly from Iterative Health's careers page and normalized into a canonical job model.