Iterative Health
Clinical Research Coordinator I - Port Arthur, TX
Port Arthur, TX · Staff+ · Full-time
Sponsorship not specifiedDetected 5 days ago
HIPAAClinical TrialsClinical ResearchFDA RegulatoryResearchCommunicationProblem Solving
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.
- Lead patient recruitment activities, e.g., performing chart reviews, discussing protocols with patients, and verifying the informed consent documentation
- Dispense study medication, collect vital signs and perform ECGs
- Perform blood draws, process and ship specimens per study protocol and IATA regulations
- complete and maintain documentation study files including, but not limited to, consent forms, source documentation, progress notes if applicable, case report forms, and investigational accountability forms.
- Maintain ongoing communication with the CRO, sponsor, research participants, Site Manager and PI throughout course of the study
- Ensure relevant study and subject specific information is entered into the CTMS system on a regular basis; complete and maintain documentation study files including, but not limited to, consent forms, source documentation, progress notes if applicable, case report forms, and investigational accountability forms.
- Perform quality work within deadlines with or without direct supervision
- The CRC supports, facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study.
Requirements
- Minimum 1-2 years of clinical research experience
- Ability to read, interpret, and apply clinic policies and research protocols
- Ability to use standard office software
- Must be able to lift up to 25 pounds
- Medical Assistant, LPN, Associates or Bachelor's degree in a clinical or scientific-related discipline preferred
- Able to execute on research tasks with guidance from more experienced staff, PIs, and management
- Strong written and verbal communication skils
Benefits
- Today, Iterative Health is headquartered in Cambridge, Massachusetts, and New York City with 250+ employees world-wide.
- Complete and maintain case report forms per FDA guidelines, and review them against the patient's medical record for completeness and accuracy
- Iterative Health Expectations
Company info
- Interact professionally with other employees, customers and suppliers
- We are seeking a full-time, experienced Clinical Research Coordinator (CRC).
Visa & Work Authorization
- Maintain ongoing communication with the CRO, sponsor, research participants, Site Manager and PI throughout course of the 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.