Iterative Health
Clinical Research Coordinator I - Nurse
Asheville, NC
Sponsorship not specifiedDetected 1 day ago
GCPHIPAAClinical TrialsClinical ResearchFDA RegulatoryResearchCommunicationProblem SolvingOrganizational SkillsGxP
> stay_score
odds of building a lasting career here
25Risky
Cap-exempt (no lottery)0
Sponsors this role35
Entry-level history0
PERM / green-card track0
Lottery odds40
Fits your clock70
Thin sponsorship signal and lottery-bound. A low-probability bet with your clock running. Prioritize cap-exempt roles and proven entry-level sponsors first.
Lottery odds assume a STEM candidate.
Personalize to your clock →> community_outcomes
No reports yet — be the first to help the next applicant.
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.
Benefits
- Complete and maintain case report forms per FDA guidelines, reviewing them against patient medical records for completeness and accuracy.
Company info
- At Iterative Health, we're actively working towards creating an environment that is representative of the diversity of patients our technology serves.
Visa & Work Authorization
- Maintain ongoing communication with the CRO, sponsor, research participants, Site Manager, and PI throughout the course of each study
Apply directly at Iterative Health →Create a free account for alerts like thisView Iterative Health immigration profile
This listing is sourced directly from Iterative Health's careers page and normalized into a canonical job model.