Clinical Research Coordinator Promed Hospital
Promed Hospital
Office Location
Full Time
Experience: 3 - 3 years required
Pay:
Salary Information not included
Type: Full Time
Location: Chennai
Skills: Protocol Development, Data Collection, Regulatory Compliance, Budget Management, Team Coordination, Quality Assurance, Continuous improvement, Innovation, Clinical trial protocols, Participant Recruitment, Patient Safety Monitoring, Stakeholder Communication
About Promed Hospital
Job Description
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,