Responsibilities
- Evaluate potential participants for study eligibility in alignment with protocol criteria
- Keep precise and up-to-date records including case report forms, source documents, study files, and regulatory paperwork
- Offer guidance, instruction, and daily supervision to junior coordinators and research assistants
- Ensure all research operations follow protocol specifications, Good Clinical Practice standards, sponsor mandates, and relevant legal and institutional guidelines
- Gather, verify, and input study data with strong accuracy and meticulous attention to detail
- Assist leadership in interviewing, selecting, onboarding, and training new team members
- Support study initiation, ongoing management, and conclusion processes across assigned projects and team efforts
- Work jointly with research investigators, sponsors, contract research organizations, and internal units to ensure smooth operations and resolve issues
- Show independent judgment in organizing tasks and adjusting to evolving study demands
- Act as a go-to reference for team staff on study workflows, protocol rules, and site-specific procedures
Work Arrangement
On-site
