Clinical Research Coordinator Job in Rochester (Minnesota, USA, United States)

Job Description:

Analyzes and develops a study protocol. Manages all phases of studies. Serves as an expert resource and mentors other internal and external study/protocol personnel. Troubleshoots and resolves problems and contributes significantly to discussions on research study design, overall project management, and study results. Participates in designing, organizing, and monitoring protocols including budget elements. Writes sections of grant applications, abstracts/posters, and manuscripts. Participates in the education of staff in areas required to carry out the #

Basic Qualifications:

Bachelor’s degree in a business, science or healthcare field required with a minimum of three years of experience in a clinical research setting.

Other Qualifications:

Graduate or diploma from a study coordinator training program is preferred. Medical terminology course preferred. SoCRA or ARCP certification is preferred.

Benefit Eligible: Yes
Exemption Status: Non-Exempt
Hours/Pay Period: 40 to 80
Schedule Details: Monday - Friday
Compensation Detail: Education, experience, and tenure may be considered along with internal equity when job offers are extended. The minimum pay rate is $19.11 per hour.
Staffing Specialist: Brent Helgren

Mayo Clinic is an affirmative action / equal opportunity educator and employer.