Senior Clinical Research Coordinator

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.

Associate's degree with 6 years' experience in clinical research or related field OR Bachelor's degree with 3 years' experience in clinical research with primary responsibility in FDA regulated clinical trials OR Bachelor's degree with 4 years' experience in clinical research OR Relevant Master's degree with 1 year of experience in clinical research.

SoCRA or ACRP certification preferred.