Clinical Research Coordinator II - Nurse

Southlake, United StatesOn-site

Responsibilities

Lead patient recruitment activities, e.g., 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
Perform blood draws, process and ship specimens per study protocol and IATA regulations
Monitor patients’ IV medications and tubing.
Monitor patients during infusion and discharge patients as policies indicate.
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.
Maintain ongoing communication with the CRO, sponsor, research participants, Site Manager and PI throughout course of 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
Schedule and prepare for monitor visits
Complete and maintain case report forms per FDA guidelines, and review them against the patient’s medical record for completeness and accuracy
Perform quality work within deadlines with or without direct supervision

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.
Solid nursing background, concentration, or willingness to obtain advanced knowledge in GI specialty
Ability to own issues and problem solve independently •
Experience in phlebotomy preferred
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

experience more accessible to you, please contact CandidateAccommodations@iterative.health.
experience more accessible to you, please contact CandidateAccommodations@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.
The Iterative Health Site Network is a premier network of 80+ global clinical research sites accelerating the path to market for gastrointestinal (GI) and hepatology novel therapies.
The CRC 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.
Able to manage an increased number of studies and/or more complex studies
Dispense study medication, collect vital signs and perform ECGs
If assigned, place IVs, administer IV medication, and fluids according to protocol.
Give intramuscular and subcutaneous injections according to protocol.