Clinical Research Coordinator

As an Assistant in this role, you will assist in the coordination and conduct of clinical trials under supervision. Your key responsibilities will include: - Supporting patient recruitment, screening, and enrollment according to protocol criteria - Scheduling and managing patient visits, sample collection, and follow-ups - Collecting and accurately entering data into Case Report Forms (CRFs) or Electronic Data Capture (EDC) systems - Maintaining essential documents in the Investigator Site File (ISF) - Ensuring adherence to study protocols, ICH-GCP, and regulatory requirements - Assisting in the preparation for audits or monitoring visits - Communicating with sponsors, CROs, and ethics committees as needed - Ensuring timely reporting of adverse events and protocol deviations - Supporting inventory management of study drugs, lab kits, and trial materials Qualifications required for this position include: - Background in healthcare, life sciences, or related field - Knowledge of clinical trial processes and regulations - Strong attention to detail and organizational skills - Good communication and interpersonal abilities - Ability to work effectively in a team environment (Note: No additional details of the company were mentioned in the provided job description),