• Independently directs large, complex, multi-center clinical research protocols/programs in collaboration with the principal investigator and in compliance with regulatory laws and institutional guidelines. 
• In collaboration with the principal investigator, researches, develops, and submits to appropriate agencies the study protocol in support of research programs. 
• 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. 
• Manages research activities and subject participation including screening, enrollment, and recruitment. 
• Identifies, reviews, and reports adverse events, protocol deviations, or other unanticipated problems appropriately. 
• Oversees and monitors research data to maintain quality. 
• Performs administrative and regulatory duties related to the study as assigned. 
• Applies statistical/analytical methods to studies and contributes to/authors/co-authors grant applications, abstracts/posters, and manuscripts. 
• May present research results/abstracts internally and externally. 
• Represents Mayo and principal investigator at meetings and in the administration of research protocols. 
• Educates and serves as an expert resource for other research personnel that may include residents and fellows. In addition to technical duties above, this position serves as the working supervisor over study coordinators in a program or across multiple programs. 
• Supervisory duties performed will vary based on the percentage of time dedicated to supervision. 
  

***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/related experience OR 
• Associate's degree/college Diploma/Certificate Program with 5 years of experience in clinical research/related field OR 
• Bachelor's degree with 3 years of experience in clinical research OR 
• Master's degree with 1 year of experience in clinical research.
  
  

Additional Qualifications

• Master's degree preferred. 
• Experience/responsibility in FDA regulated clinical trials is preferred.
  

License or Certification

• SoCRA or ACRP certification preferred.