Clinical Research Coordinator

*THIS IS A PART TIME CONTRACT POSITION ~25 HOURS PER WEEK* 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, technically savvy, and experienced in 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 to 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. Experience working with human research participants and clinical trial data collection. Strong proficiency with EDC systems and general clinical trial technology. Tech-savvy with the ability to quickly learn new systems, software, and processes. Comfortable reviewing data/files, navigating study documentation, and locating information independently. Clinical documentation and data management experience and training on best practices. Excellent written, verbal, and interpersonal communication skills. Ability to work independently, efficiently, and ramp up quickly in a fast-paced environment. Medical device experience preferred, but not required. #J-18808-Ljbffr Redbock - an NES Fircroft company