Supervisor - Senior Clinical Research Coordinator - Cardiovascular Research
Job ID 342965 Date posted 10/01/2024- Rochester, MN
- Full Time
- Research
- Remote: No
Mayo Clinic is top-ranked in more specialties than any other care provider according to U.S. News & World Report. 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
- 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. In addition to technical duties above, this position serves as the working supervisor over study coordinators in a program or across multiple programs.
- Supervisory duties performed will vary based on the percentage of time dedicated to supervision.
***Visa sponsorship is not available for this position. This position is not eligible for F-1 OPT STEM extension.***
Qualifications
- HS Diploma with at least 7 years of clinical research coordination/related experience OR
- Associate's degree/college Diploma/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 Qualifications
- Master's degree preferred.
- Experience/responsibility in FDA regulated clinical trials is preferred.
License or Certification
- SoCRA or ACRP certification preferred.
Exemption Status
Exempt
Compensation Detail
Education, experience and tenure may be considered along with internal equity when job offers are extended.
Benefits Eligible
Yes
Schedule
Full Time
Hours/Pay Period
80 hours
Schedule Details
Monday thru Friday, between the hours of 6 am to 6 pm
Weekend Schedule
None
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
Chad Musolf
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