Listed on Nemours Foundation’s own careers site. You apply with them directly — we never stand between you and the employer.
What this role is
This role supports clinical research operations by managing the administrative, regulatory, and participant-facing aspects of research studies and trials. It suits someone organized and detail-oriented who can juggle compliance paperwork, participant recruitment and education, data management, and coordination with sponsors and auditors.
Our summary, not Nemours Foundation’s wording. The full posting is on their site.
What they ask for
Required
- Assist with regulatory document preparation and collection
- Recruit and enroll study participants
- Obtain informed consent, assent, and parental permission forms
- Educate participants and parents about study procedures
- Schedule and conduct study procedures
- Collect and record study data accurately
- Maintain detailed study records and databases
- Coordinate with study sponsors
- Participate in sponsor monitoring visits
- Prepare for and participate in research audits