Job Description

We are seeking an experienced Clinical Research Coordinator (CRC) with over 4 years of experience to join our dynamic site network. The CRC will play a crucial role in coordinating and managing clinical trials, ensuring compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines. The ideal candidate will have a strong background in clinical research, excellent organizational skills, and a passion for patient care.

Key Responsibilities:

• Coordinate and oversee all aspects of clinical trials, from initiation to completion, ensuring adherence to study protocols and regulatory requirements.
• Recruit, screen, and enroll study participants according to inclusion and exclusion criteria.
• Obtain informed consent from study participants and provide detailed information about the study procedures.
• Schedule and conduct study visits, collect data, and maintain accurate and complete source documentation.
• Administer study-related procedures and assessments, 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.

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