Clinical Research Coordinator - SW Wisconsin
Position description
- Independently coordinates complex (i.e. interventional, therapeutic greater than minimal risk) clinical research protocols with minimal direction from the principal investigator and/or supervisor in compliance with regulatory laws and institutional guidelines.
- Collaborates with research team to assess feasibility and management of research protocols.
- Ensures implementation of research protocols after IRB approval and provides information as appropriate for progress reports.
- Screens, enrolls, and recruits research participants.
- Coordinates schedules and monitors research activities and subject participation. Identifies, reviews, and reports adverse events, protocol deviations, and other unanticipated problems appropriately.
- Manages, monitors, and reports research data to maintain quality and compliance.
- Provides education/training for others within the department.
- Performs administrative and regulatory duties related to the study as appropriate.
- Some travel may be required.
Qualifications
HS Diploma with at least 7 years of clinical research coordination experience or related experience OR
Associate's degree with at least 2 years clinical research coordination experience or related experience
OR
Bachelors with at least 1 year of experience in clinical research or related experience.
Preferred additional qualifications
Graduate or diploma from a study coordinator training program is preferred. Medical terminology course preferred. SoCRA or ARCP certification is preferred.
Pay range
$24.03 - $35.62 / hour
Schedule details
Day shift
Monday to Friday
Flexible 8 hour day shifts, starting at 7:00am, 7:30am, or 8:00am, based on patient need.