Clinical Research Coordinator

As a Protocol Development & Compliance Specialist, your role involves developing and adhering to comprehensive clinical trial protocols in collaboration with the Principal Investigator. You will be responsible for participant recruitment and retention by implementing effective strategies. Your key responsibilities include: - Overseeing accurate and timely data collection entry and management - Ensuring all trial activities comply with regulatory guidelines and maintaining thorough documentation - Managing the clinical trial budget effectively to ensure cost efficiency - Coordinating with cross-functional teams and providing necessary training to staff involved in the trial - Monitoring participant safety and managing adverse events promptly - Implementing quality control measures to ensure trial integrity - Maintaining effective communication with stakeholders, including sponsors, regulatory bodies, and the Principal Investigator In addition to the above responsibilities, you will be expected to identify opportunities for process improvements. The job type is Full-time, Permanent with benefits including Provident Fund. The work location is in person with a fixed shift schedule.,