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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 position that has been approved for one year that may have 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.***
Additional Qualifications
License or Certification
Required Experience:
Senior IC
Part-Time