Clinical Research Coordinator - SW Wisconsin

Company: Mayo Clinic
Location: La Crosse
Posted on: June 23, 2022

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