Responsibilities
- Handles, prepares, administers, and manages inventory of investigational products as required.
- Delivers patient education and consultations in outpatient environments under physician oversight for clinical trials.
- Follows assigned research study protocols accurately and consistently.
- Keeps accurate and timely records, including source documentation.
- Ensures all clinical tasks comply with research protocols, regulations, and legal standards.
- Works collaboratively with healthcare teams, sponsors, contract research organizations, and vendors.
- Engages in clear communication with study participants and their designated caregivers or support persons.
- Attends and completes all required training sessions, including ongoing professional development activities.
- Completes assigned training modules, including mandatory Good Clinical Practice certification.
