Clinical Research Coordinator

We are seeking a proactive, attention to detail, highly motivated and enthusiastic Clinical Research Coordinator to join our dynamic research team. The Clinical Research Coordinator will play a critical role in setting up and running clinical studies and contributing to the advancement of diabetes research. If you are passionate and experienced in research and have a strong desire to make a positive impact in the field of diabetes, this is an opportunity for you. Clinical Research Coordinator Responsibilities & Duties Conduct diabetes clinical research studies, including protocol development, regulatory submissions, data collection, and documentation. Schedule and oversee participant visits, ensuring protocol adherence and participant safety. Coordinate and collaborate with multidisciplinary team, including doctors, nurses, and other healthcare professionals. Maintain meticulous study documentation, ensuring data integrity through accurate entry, verification, and audit readiness. Monitor study progress, identify risks or deviations, and implement corrective actions promptly. Manage clinical research studies in accordance with regulatory and institutional policies. Create documentation for ethics submissions and set up and maintain the Investigator Site File (ISF). Clinical Research Coordinator Qualifications & Skills Proven experience in a clinical research setting, ideally in a coordination or protocol management role. Clinical experience in diabetes. Strong understanding of GCP, ICH guidelines, and regulatory requirements. Ability to work collaboratively in a team environment. Demonstrated ability to write and review clinical protocols and related study documents. Exceptional attention to detail and commitment to maintaining data integrity. Strong organisational skills with the ability to manage multiple studies simultaneously. Excellent communication skills for working with multidisciplinary teams and external stakeholders. Required: Minimum of 3 years of experience in clinical research. Strong knowledge of Good Clinical Practice (GCP) and regulatory requirements. Excellent written and verbal communication skills. Preferred: Diabetes Clinical Nurse Specialist. Credentialled Diabetes Educator. Previous experience in diabetes medical devices and clinical settings. Experience with electronic data capture systems. #J-18808-Ljbffr