Clinical Research Coordinator - SW Wisconsin
Company: Mayo Clinic
Location: La Crosse
Posted on: June 23, 2022
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Job Description:
**Why Mayo Clinic**Mayo Clinic is the nation's best hospital
(U.S. News & World Report, 2021-2022) and ranked #1 in more
specialties than any other care provider. We have a vast array of
opportunities ranging from Nursing, Clinical, to Finance, IT,
Administrative, Research and Support Services to name a few. Across
all locations, you'll find career opportunities that support
diversity, equity and inclusion. At Mayo Clinic, we invest in you
with opportunities for growth and development and our benefits and
compensation package are highly competitive. We invite you to be a
part of our team where you'll discover a culture of teamwork,
professionalism, mutual respect, and most importantly, a
life-changing career!Mayo Clinic offers a variety of employee
benefits. For additional information please visit Mayo Clinic
Benefits (https://jobs.mayoclinic.org/benefits/) . Eligibility may
vary.**Position description**+ Independently coordinates complex
(i.e. interventional, therapeutic greater than minimal risk)
clinical research protocols with minimal direction from the
principal investigator and/or supervisor in compliance with
regulatory laws and institutional guidelines.+ Collaborates with
research team to assess feasibility and management of research
protocols.+ Ensures implementation of research protocols after IRB
approval and provides information as appropriate for progress
reports.+ Screens, enrolls, and recruits research participants.+
Coordinates schedules and monitors research activities and subject
participation. Identifies, reviews, and reports adverse events,
protocol deviations, and other unanticipated problems
appropriately.+ Manages, monitors, and reports research data to
maintain quality and compliance.+ Provides education/training for
others within the department.+ Performs administrative and
regulatory duties related to the study as appropriate.+ 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. blood
collection kits, data collection booklets, use of CRU, etc.), and
verification of content to meet institutional and federal
standards; communication with study sites and/or federal agencies
regarding study status changes; Federal and Institutional Review
Board (IRB) document preparation and submission; and provides
consultative expertise regarding regulatory and policy
requirements.+ 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.+ 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 F-1 OPT STEM
extension.*******Qualifications**HS Diploma with at least 7 years
of clinical research coordination experience or related experience
OR Associate's degree with at least 2 years clinical research
coordination experience or related experience OR Bachelors with at
least 1 year of experience in clinical research or related
experience.**Additional qualifications**Graduate or diploma from a
study coordinator training program is preferred. Medical
terminology course preferred. SoCRA or ARCP certification is
preferred.**License or certification**N/A**Exemption
status**Non-exempt**Compensation Detail**$24.03 - $35.62 /
hour**Benefits eligible**Yes**Schedule**Full Time**Hours / Pay
period**80**Schedule details**Day shiftMonday to FridayFlexible 8
hour day shifts, starting at 7:00am, 7:30am, or 8:00am, based on
patient need.**Weekend schedule**No**International
Assignment**No**Site description**La Crosse, WI, is a city of
52,000 with a metro area of 120,000 in the Upper Mississippi River
Valley, located between Minneapolis/St. Paul, MN, and Madison, WI.
The area offers unlimited, four-season recreational opportunities
(biking, golf, hiking the bluffs and cross-country/downhill
skiing). We have a great family environment with safe and
high-quality schools, including two universities and a technical
college. There are sport events, a local symphony orchestra,
theaters, children's museum and a civic
center.**Recruiter**Chadwick Musolf**EOE**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.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.**Equal opportunity**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.
Keywords: Mayo Clinic, La Crosse , Clinical Research Coordinator - SW Wisconsin, Healthcare , La Crosse, Wisconsin
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