CRC

Job Summary:

We are seeking a proactive and driven Clinical Research Coordinator (CRC) to join our dynamic clinical research team. The ideal candidate will have hands-on experience managing studies from start-up to close-out and a background in working within private clinical research settings. If you are a go-getter with a passion for clinical research and a proven track record in coordinating studies, we want to hear from you!

Key Responsibilities:

• Coordinate and oversee all aspects of clinical trials from initiation to close-out, ensuring adherence to study protocols and regulatory requirements.
• Proactively manage study timelines, deliverables, and resources to ensure successful study completion.
• Recruit, screen, and enroll study participants according to inclusion and exclusion criteria.
• Obtain informed consent from study participants and provide detailed information about study procedures.
• Schedule and conduct study visits, collect data, and maintain accurate source documentation.
• Perform study-related procedures, including vital signs, ECGs, blood draws, and other clinical evaluations as required by the protocol.
• Monitor patient safety, report adverse events, and ensure timely follow-up with study participants.
• Enter and manage study data in electronic data capture (EDC) systems, ensuring data integrity and accuracy.
• Prepare for and participate in site monitoring visits, audits, and regulatory inspections.
• Collaborate with investigators, study sponsors, and other research staff to ensure smooth study operations.
• Maintain up-to-date knowledge of GCP, ICH guidelines, and relevant regulatory requirements.
• Provide exceptional patient care and maintain a positive, professional relationship with study participants.