Clinical Research Coordinator - Orthopedics

The Mayo Clinic Orthopedics Research Department is seeking an individual who is passionate or has knowledge in the hockey field and who is comfortable traveling between local ice arenas and meeting players at rinks during the critical hours of 47pm 1 or 2 days a week with the occasional weekend.

As a Clinical Research Coordinator you will:

• Independently coordinate 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.
• Collaborate with research team to assess feasibility and management of research protocols.
• Ensure implementation of research protocols after IRB approval and provide information as appropriate for progress reports.
• Screen enroll and recruit research participants.
• Coordinate schedules and monitor research activities and subject participation.
• Identify review and report adverse events protocol deviations and other unanticipated problems appropriately.
• Manage monitor and report research data to maintain quality and compliance.
• Provide education/training for others within the department.
• Perform administrative and regulatory duties related to the study as appropriate.
• Be involved with protocol development and maintenance activities with responsibilities that 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 provide consultative expertise regarding regulatory and policy requirements.
• Accurately apply 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.
• Participate in other protocol development activities and execute other assignments as warranted and assigned.

***Visa sponsorship is not available for this position. This position is not eligible for F1 OPT STEM extension.***

• HS Diploma with at least 5 years of clinical research coordination/related experience OR
• Associates degree/college Diploma/Certificate Program with at least 3 years of experience Associates in Clinical Research from an accredited academic institution without experience OR
• Bachelors with at least 1 year of experience or completion of a Mayo Clinicsponsored clinical research internship in lieu of 1 year of experience.
• Experience should be in the clinical setting or related experience.
  
  

Additional Qualifications

• Prefer an experienced clinical research coordinator with a deep understanding of IRB submissions particularly given the tight timelines involved as well as significant Sponsor communications.
• Strong knowledge in the field of clinical research coordination
• Graduate or diploma from a study coordinator training program is preferred.
• One year of clinical research experience is preferred.
• Medical terminology course is preferred.