Clinical Research Coordinator

Clinical Research Coordinator (Part-time, 4-months w/ possibility of extension) Overview Our client needs a Clinical Research Coordinator (CRC) to support an ongoing study. This role is responsible for patient-facing coordination, study start up, source documentation, data management, and handling clinical supplies. The ideal candidate is highly organized, comfortable engaging with patients, and experienced in EDC-based clinical trial support. Key Responsibilities Contact patients to schedule study visits, confirm appointments, and ensure visit completion. Properly handle source documents and make necessary corrections paper based documents. Track, prepare, and handle clinical supplies going in and out to patients. Conduct remote evaluations and distribute patient surveys per protocol requirements. Perform timely and accurate data entry into EDC and resolve data queries. Follow up on adverse events, collect relevant information, and elevate as needed. Maintain clear, professional communication with patients, investigators, and internal teams. Ensure compliance with protocol, GCP, and study documentation requirements. Qualifications 1-3 years experience as a Clinical Research Coordinator with a life science organization (preferable medical device). Strong comfort interacting with patients via phone, video, and electronic tools. Proficiency with EDC systems and general clinical trial technology. Excellent written, verbal, and interpersonal communication skills. Clinical documentation and data management experience and training on best practices. Ability to work independently and learn quickly in a fast-paced environment #J-18808-Ljbffr Redbock - an NES Fircroft company