Clinical Research Coordinator

Protocol Development & compliance Develop and adhere to comprehensive clinical trial protocols in collaboration with the Principal Investigator Participant Recruitment and Retention Implement effective strategies to recruit and retain study participants Data collection & management Oversee accurate and timely data collection entry and management Reguatory compliance and documentation Ensure all trial activities comply with regulatory guidelines and maintain thorough documentation Budget Management Manage the clinical trial budget effectively, ensuring cost efficiency. Team Coordination and Training Co-ordinate with cross-functional teams and provide necessary training to staff involved in the trial Patient safety monitoring Monitor participant safety and manage adverse events promptly Quality Assurance Implement quality control measures to ensure trial integrity Stakeholder Communication Maintain effective communication with stakeholders, including sponsors, regulatory bodies and the PI (Principal investigators) Continuous Improvement & Innovation Identify opportunities for process improvements Job Types: Full-time, Permanent Benefits: Provident Fund Schedule: Fixed shift Work Location: In person