Roles and Responsibilities :
Participant Management
- Responsible for participant recruitment, informed consent process, and regular follow-ups as per study protocol.
Field Work & Sample Collection
Conduct field visits for community-based or site-based recruitment and collect biological samples such as swabs, blood, etc., adhering to study-specific protocols and safety procedures.Monitoring & Coordination
Assist senior team members with coordination of clinical trial activities, including scheduling and conducting monitoring visits.Training & Compliance
Undergo training on Good Clinical Practice (GCP) and study-specific procedures; train site personnel on GCP and protocol adherence.Documentation & Support
Maintain accurate records of all participant interactions and sample collections; support the team with any other study-related tasks as needed.Skills Required
Clinical Assessment, care coordination , Patient Education, Data Analysis, Regulatory Compliance, Quality Improvement