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