Iterative Health is looking to solve the problem of accelerating clinical research to transform patient outcomes in the field of gastrointestinal (GI) and hepatology novel therapies.
Requirements
Computer skills - Microsoft Word, Excel, PowerPoint, CTMS, EMR
Previous experience in a role of complex administration or project coordination
Phlebotomy: 1 year (Required)
Medical Assistant or LPN required
Associates degree in a clinical or scientific-related discipline preferred
1+ years previous experience as a clinical research coordinator for pharmaceutical phase II or III trials, GI trials experience preferred
Responsibilities
Administratively and clinically manage industry-sponsored clinical trials
Adhere to Research SOP’s, Good Clinical Practices, and the study protocols
Assist in training site personnel in regulatory, lab procedures, and general study-related training
Perform blood draws, process and ship blood/urine specimens per study protocol and IATA regulations
Dispense study medication, collect vital signs and perform ECGs
Assist with routine data verification and quality control, ensuring data integrity and consistency with prescribed study protocol
Complete and maintain case report forms per FDA guidelines, and review them against the patient’s medical record for completeness and accuracy
Other
Medical Assistant or LPN required
Associates degree in a clinical or scientific-related discipline preferred
Effective communication skills to include written, verbal ,and presentation skills
Strong attention to detail and organizational, analytical, and problem-solving skills, an agile sense of prioritization and urgency
Periodic local travel to other practice locations on an as-needed basis