Senior Clinical Research Coordinator - Nursing Research - Limited Tenure

About Mayo Clinic

Mayo Clinic is top‑ranked in more specialties than any other care provider according to U.S. News & World Report. We prioritize the needs of patients while investing in competitive compensation and comprehensive benefit plans—providing care for you and your family, now and in the future. With continuing education and advancement opportunities at every turn, you can build a long, successful career with Mayo Clinic.

City:
Rochester

State: MN

Remote:
No

Department:
Nursing

• Medical:
  Multiple plan options.
• Dental:
  Delta Dental or reimbursement account for flexible coverage.
• Vision:
  Affordable plan with national network.
• Pre‑Tax Savings: HSA and FSAs for eligible expenses.
• Retirement:
  Competitive retirement package to secure your future.

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.

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.

Minimum Education and/or Experience

Required:

• HS Diploma with at least 7 years of clinical research coordination/related experience OR

• Associate's degree, college diploma, or 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:

• Master’s degree preferred.

• Experience/responsibility in FDA‑regulated clinical trials is preferred.

• SoCRA or ACRP certification preferred.

Compensation range is $67,454.40 – $ per year.

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender identity, sexual orientation, national origin, protected veteran status, or disability status. Mayo Clinic participates in E‑Verify and may provide the Social Security Administration and, if necessary, the Department of Homeland Security with information from each new employee’s Form I‑9 to confirm work authorization.