Clinical Research Coordinator

Job Summary :

Continental Hospitals is seeking a dedicated and experienced Clinical Research Coordinator with a minimum of 3 years of experience in clinical trials . The ideal candidate will be responsible for the coordination, management, and execution of clinical research studies in compliance with applicable regulations, protocols, and institutional policies.

Key Responsibilities :

• Study Coordination : Oversee day-to-day operations of clinical research projects, ensuring smooth and efficient execution from initiation through completion.
• Subject Recruitment & Enrollment : Manage the recruitment and enrollment process for study participants, ensuring they meet all inclusion / exclusion criteria.
• Data Collection & Management : Ensure accurate and timely collection of study data, and maintain complete, organized, and compliant study documentation.
• Compliance & Protocol Adherence : Ensure all clinical trials are conducted according to Good Clinical Practice (GCP), ICH guidelines, and regulatory requirements. Monitor adherence to the study protocol and make necessary adjustments as needed.
• Patient Care Coordination : Communicate with study participants regarding their visits, procedures, and any other relevant study information. Ensure proper follow-up, including adverse event reporting and participant safety.
• Collaborative Coordination : Liaise with internal and external stakeholders, including research teams, physicians, and regulatory bodies, to facilitate the successful completion of clinical trials.
• Regulatory Documentation : Prepare and maintain all regulatory documentation, including informed consent forms, case report forms, ethics committee submissions, and sponsor-related documentation.
• Quality Assurance : Conduct routine site visits and audits, ensuring compliance with all study-related activities and providing corrective actions where necessary.
• Training & Mentorship : Train and mentor junior research staff and new hires in clinical trial processes, protocols, and GCP standards.

Qualifications :

Preferred Qualifications :