Role Overview: As a Senior Clinical Research Coordinator at the company, you will oversee the daily activities of clinical trials at the Nagpur location. Your main responsibilities will include coordinating and supervising the informed consent process, ensuring compliance with protocols, handling documentation and records, liaising with participants, researchers, and medical staff, maintaining trial-related information, and ensuring trials are conducted ethically and in compliance with regulatory standards. Key Responsibilities: - Coordinating and supervising the informed consent process - Ensuring compliance with protocols - Handling all documentation and records related to research - Liaising with participants, researchers, and medical staff - Maintaining trial-related information - Ensuring trials are conducted in compliance with ethical and regulatory standards Qualifications Required: - Experience in Clinical Research, Clinical Trials, and Research - Knowledge of Informed Consent and Protocol implementation - Strong organizational and documentation skills - Excellent communication and interpersonal skills - Ability to work collaboratively with a diverse team - Previous leadership experience in clinical research is an advantage - Bachelor's or advanced degree in a related field such as Life Sciences, Nursing, or Allied Health,

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Senior Clinical Research Coordinator