Associate Clinical Research Coordinator - Comprehensive Cancer Center
Associate Clinical Research Coordinator - Comprehensive Cancer Center
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Not Disclosed
Salary Not Disclosed
1 Vacancy
Job Description
- Coordinates nontherapeutic (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.
***Visa sponsorship is not available for this position. This position is not eligible for F1 OPT STEM extension.***
**This position is 50 or more remote and requires the candidate to live within driving distance of the Mayo Clinic campus in Rochester Minnesota.**
**During the selection process you will participate in anOnDemand (prerecorded)interviewthatyou can complete at your convenience. During the OnDemandinterview a question will appear on your screen and you will have time to consider eachquestion before responding. You will have the opportunity to rerecord your answer toeach question Mayo Clinic will only see the final recording. The complete interviewwillbe reviewed by a Mayo Clinic staff member and you will be notifiedof next steps.**
Qualifications
- HS Diploma with at least 3 years of experience OR
- Associates degree/college Diploma/Certificate Program with at least 1 year of experience Associates in Clinical Research from an accredited academic institution without experience OR
- Bachelors degree. Experience should be in the clinical setting or related experience.
Additional Qualifications
- Graduate or diploma from a study coordinator training program is preferred.
- One year of clinical research experience is preferred.
- Medical terminology course is preferred.
Required Experience:
IC
Employment Type
Full-Time
