Job Description
About the position
- Responsibilities
- Coordinates activities to identify patients eligible for clinical trials.
- Pre-screens patients for placement into open and enrolling clinical trials.
- Logs pre-screening information for reporting measures on patient demographics and disease type.
- Tracks updated lists of studies with open slots, cohorts, and wait lists.
- Provides timely feedback to referring physicians and CRCs about patient eligibility.
- Acts as an educational resource regarding protocol requirements and specific disease processes.
- Works directly with unit supervisors, coordinators, program managers, primary investigators, and research leadership.
- Requirements
- Registered Nurse licensure required.
- Basic Life Support Certification required.
- Three to five years of recent research experience required.
- Minimum of two years' experience in the Mayo Clinic system preferred.
- Knowledge of Institutional Review Board Guidelines, FDA Code of Federal Regulations, and ICH/GCP Guidelines required.
- Strong written communication skills required.
- Computer knowledge and skills required.
- Technical and analytical skills in the use of complex medical equipment.
- Nice-to-haves
- Certification through a national research organization (ACRP, SOCRA) preferred.
- Demonstrated ability to train, assist, and educate coordinators as necessary.
- Benefits
- Opportunities for advancement
- Comprehensive benefit plans
- Support for continuing education
Apply Now
Apply Now