Clinical Research Coordinator

We are looking for a Clinical Research Coordinator to support clinical trial activities, patient coordination, documentation, regulatory compliance, and study-related communication. The candidate should have knowledge of clinical research basics, ethical guidelines, data documentation, and patient interaction. This is suitable for candidates who are organized, detail-focused, and interested in healthcare research operations within a hospital environment.

Role & Responsibilities:

• Assist investigators and research teams in daily clinical research study activities.
• Coordinate patient screening, enrollment, follow-up visits, and study schedules.
• Maintain accurate study documentation, source records, and case report forms.
• Support informed consent process as per ethical and regulatory guidelines.
• Coordinate with patients, doctors, sponsors, monitors, and ethics committee teams.
• Ensure study procedures are conducted according to approved protocols.
• Track study visits, lab investigations, reports, and patient compliance requirements.
• Maintain confidentiality of patient records and clinical trial information.
• Assist in data entry, query resolution, and study database updates.
• Prepare and organize documents for monitoring visits, audits, and inspections.
• Report adverse events and protocol deviations to the concerned team as per process.
• Maintain study supplies, investigational product records, and trial-related logs.
• Support ethics committee submissions and regulatory documentation.
• Follow Good Clinical Practice guidelines and hospital research policies.
• Participate in training programs related to clinical trials and research compliance.