Clinical Research Coordinator I/II

Responsibilities Execute the procedures of the research protocol. Safeguard the integrity of study data. Actively participate in the screening, recruitment, and retention of clinical trial participants. Reconcile research billing, payments, and invoices. Manage supply and equipment inventory levels. Schedule logistics, determine workflows, and secure resources for defined clinical research trials. Serve as an initial point of contact for clinical research participants and clinical staff, providing information regarding research procedures, expectations, and inquiries. Ensure participants follow the research protocol and alert Principal Investigator of issues. Requirements Demonstrated ability to work independently and collaborate effectively with physicians, coordinators, sponsors, and multidisciplinary teams. Demonstrated ability to manage multiple priorities simultaneously and consistently meet deadlines in a fast‑paced environment. Strong verbal and written communication skills with demonstrated attention to detail and sound professional judgment. Working knowledge of medical terminology. Demonstrated organizational skills and proficiency with Microsoft Office applications, including Word and Excel. Demonstrated problem‑solving and conflict‑resolution skills. Ability to reliably travel between multiple work sites with dependable transportation. Current ACRP or SoCRA Certification or ability to become certified within 6 months of hire. Certifications & Qualifications ACRP Certification SoCRA Certification #J-18808-Ljbffr