Clinical Research Coordinator

Role Overview: As a Clinical Research Coordinator at Concept Clinical Service in Surat, your primary responsibility will be to coordinate clinical trials effectively. You will play a crucial role in obtaining informed consent from participants, ensuring adherence to study protocols, managing research documentation, and maintaining regulatory compliance. Your daily tasks will involve patient recruitment, data collection, monitoring activities, and facilitating communication within the study team and investigators. Key Responsibilities: - Coordinate clinical trials efficiently - Obtain informed consent from study participants - Adhere to study protocols and ensure compliance with regulatory requirements - Manage research documentation accurately - Conduct patient recruitment activities - Collect and analyze data effectively - Monitor the progress of clinical trials - Maintain open communication with the study team and investigators Qualifications Required: - Demonstrated experience in Clinical Research and Clinical Trials - Proficiency in understanding Protocols and Regulatory Compliance - Ability to skillfully obtain Informed Consent and conduct Patient Recruitment - Strong organizational and documentation skills - Excellent communication and interpersonal abilities - Bachelor's degree in a related field (e.g., life sciences, nursing) - Previous experience in the healthcare industry and familiarity with ICH-GCP guidelines would be advantageous,