Associate Clinical Research Coordinator-Cerebrovascular Diseases Research
Job description
Mayo Clinic has been ranked the #1 hospital in the nation by U.S. News & World Report, as well as #1 in more specialties than any other care provider. As we work together to put the needs of the patient first, we are also dedicated to our employees, investing in competitive compensation and comprehensive benefit plans – to take care of you and your family, now and in the future. And with continuing education and advancement opportunities at every turn, you can build a long, successful career with Mayo Clinic. You’ll thrive in an environment that supports innovation, is committed to ending racism and supporting diversity, equity and inclusion, and provides the resources you need to succeed.
Responsibilities
Coordinates non-therapeutic (i.e. minimal risk, survey, chart review) clinical research protocols with direction from the principal investigator and/or supervisor in compliance with regulatory laws and institutional guidelines. May assist in complex (i.e. interventional, therapeutic, greater than minimal risk) studies with direction but does not have overall responsibility for these studies. Screens, enrolls, and recruits research participants. Coordinates schedules and monitors research activities and subject participation. Recognizes adverse events, protocol deviations, and other unanticipated problems and reports appropriately. Collects, abstracts, and enters research data. Performs administrative and regulatory duties related to the study as assigned. Some travel may be required.
Protocol Development and Maintenance Activities Responsibilities may include, but are not limited to: ongoing management of the protocol document and process through editing, amendments, proofing, coordination of study logistics (i.e. data collection booklets, use of CRU, etc.), and verification of content to meet institutional and federal standards; Institutional Review Board (IRB) submission; and communication with study sites and/or federal agencies regarding study status changes.
Participates in other protocol development activities and executes other assignments as warranted and assigned.
This ACRC will support the Determinants of Incident Stroke Cognitive Outcomes and Vascular Effects on RecoverY (DISCOVERY) study by performing cognitive assessments on research participants who have had strokes. Prior experience with cognitive testing and/or coordinating neurology research studies in preferred.
Qualifications
HS Diploma with at least 3 years' experience in the clinical setting or related experience including competency in Outlook, Excel, and Epic OR Associates degree or completion of a college Diploma or Certificate Program with at least 1-year experience in the clinical setting or related experience including competency in Outlook, Excel, and Epic OR Bachelor's degree, healthcare or science related field preferred.
Graduate or diploma from a study coordinator training program is preferred. One year clinical research experience preferred. Medical terminology course preferred. No licensure/certification is required.
Bilingual Spanish/English required for this position.
**This position is not eligible for visa sponsorship; Also, Mayo Clinic DOES NOT participate in the F-1 STEM OPT extension program.
Exemption Status
Nonexempt
Compensation Detail
$22.91- $33.27 / hour
Benefits Eligible
Yes
Schedule
Full Time
Hours/Pay Period
80
Schedule Details
Training to occur on site during orientation. Availability to work on a hybrid schedule after orientation/training. Standard hours: 8:00 am - 4:30 pm, Mon-Fri. Schedule may vary based on participant needs, including working past 5:00 pm.
Weekend Schedule
Occasional weekends may be required
International Assignment
No
Site Description
As an Affirmative Action and Equal Opportunity Employer Mayo Clinic is committed to creating an inclusive environment that values the diversity of its employees and does not discriminate against any employee or candidate. Women, minorities, veterans, people from the LGBTQ communities and people with disabilities are strongly encouraged to apply to join our teams. Reasonable accommodations to access job openings or to apply for a job are available.
Recruiter
Chelsea Crosby
Department Title
Research
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