Senior Clinical Research Coordinator - Nursing Research - Limited Tenure

Receives direction from principal investigator, supervisor, or other staff involved in complex, multi-center projects/research programs. Gives direction to and works cooperatively with research fellows and other research staff. Collaborates and interacts with various departments within the institution and with organizations/agencies external to Mayo. Works cooperatively with other investigators and personnel at all levels. Interacts with research participants, other research centers, and sponsoring companies to resolve problems and ensure efficient completion of research studies. 

Position Overview: (Major Functions and Non-Essential Functions): 
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. 

This is a Limited Tenure role.

Minimum Education and/or Experience Required: (Education Requirements and Experience): 
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 Experience and/or Qualifications: (Has Achieved Competency in the Following Areas, Job Knowledge and Additional Considerations):

Master's degree preferred. Experience/responsibility in FDA regulated clinical trials is preferred.
Licensure/Certification Required: 
SoCRA or ACRP certification preferred.