Clinical Research Coordinator - Limited TenureJob ID 160956BR Date posted 10/06/2021
- Rochester, Minnesota
- Full Time
- Medical Oncology
Mayo Clinic is the nation's best hospital (U.S. News & World Report, 2020-2021) and ranked #1 in more specialties than any other care provider. We have a vast array of opportunities ranging from Nursing, Clinical, to Finance, IT, Administrative, Research and Support Services to name a few. Across all locations, you’ll find career opportunities that support diversity, equity and inclusion. At Mayo Clinic, we invest in you with opportunities for growth and development and our benefits and compensation package are highly competitive. We invite you to be a part of our team where you’ll discover a culture of teamwork, professionalism, mutual respect, and most importantly, a life-changing career!
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- 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.
- Protocol Development and Maintenance Activities Responsibilities may include, but are not limited to: ongoing management of the protocol document and process through editing, amendments, proofing, coordination of study logistics (i.e. blood collection kits, data collection booklets, use of CRU, etc.), and verification of content to meet institutional and federal standards; communication with study sites and/or federal agencies regarding study status changes; Federal and Institutional Review Board (IRB) document preparation and submission; and provides consultative expertise regarding regulatory and policy requirements.
- Accurately applies investigators' scientific data into a cohesive format for the protocol document and associated procedures that are consistent with internal and external policies and regulatory requirements.
- Participates in other protocol development activities and executes other assignments as warranted and assigned.
This is a limited tenure position that has been approved for approximately one year, that may the possibility of turning into a regular position.
**Visa sponsorship is not available for this position. This position is not eligible for F-1 OPT STEM extension.**
- HS Diploma with at least 7 years of clinical research coordination experience OR
- Associate’s degree with at least 2 years clinical research coordination experience OR
- Bachelors with at least 1 year of experience in clinical research
- Graduate or diploma from a study coordinator training program is preferred.
- Medical terminology course preferred.
License or certification
Education, experience and tenure may be considered along with internal equity when job offers are extended. The minimum pay rate is $23.56 per hour.
Hours / Pay period
M-F, normal business hours
Mayo Clinic is located in the heart of downtown Rochester, Minnesota, a vibrant, friendly city that provides a highly livable environment for more than 34,000 Mayo staff and students. The city is consistently ranked among the best places to live in the United States because of its affordable cost of living, healthy lifestyle, excellent school systems and exceptionally high quality of life.
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