Iterative Health is seeking to accelerate clinical research for gastrointestinal (GI) and hepatology novel therapies by empowering research teams and study sponsors through tech-enabled services. The Clinical Research Coordinator II will support the success and growth of partner sites by managing clinical trial activities.
Requirements
- Medical Assistant, LPN, Associates or Bachelor’s degree in a clinical or scientific-related discipline preferred
- Minimum 3 years of clinical research experience
- Experience in phlebotomy preferred
- Ability to read, interpret, and apply clinic policies and research protocols
- Ability to use standard office software
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 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
- Perform blood draws, process and ship specimens per study protocol and IATA regulations
- 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.
Other
- Strong written and verbal communication skills
- Must be able to lift up to 25 pounds
