Key skills
CommunicationCollaboration
About this role
Role Overview
- Recruit, screen, enroll, and obtain informed consent from study participants
- Maintain Volunteer database and manage recruitment efforts
- Coordinate and oversee research sessions
- Ensure compliance with the study protocol and internal processes
- Maintain all study documentation
- Assist Principal Investigator with Ethics Committee applications
- Conduct training and provide guidance to study staff
- Serve as main point of contact for research volunteers
- Maintain facilities and track spend
- Implement process improvement activities as needed
Requirements
- Bachelor's degree in social, life science, or research related fields
- Previous experience with a minimum of 1 year in clinical research
- Outstanding organizational skills
- Proficient at Microsoft Office (Excel, Outlook, Word)
- Meticulous attention to detail
- Excellent communication skills (written and verbal)
Benefits
- Total Rewards designed to unlock ambition
- Health insurance
- Flexible working arrangements
- Support for career opportunities in a culture that fosters collaboration