Job OverviewJob OverviewIn this role, you will:Partner with our Recruitment team to develop tools that help recruiters screen potential participants. This includes a thorough understanding of the trial criteria for participation, an understanding of the disease under study and our local population, the fit with current research portfolio, and any external resources that may be needed Conduct a detailed analysis of study protocol to support budget/contract negotiationsIdentifies and recommends start-up enrollment goals and recruitment strategies Creates study-specific tools in the EMR-Epic and materials for protocol implementationCollaborates with team members in preparing regulatory documents, including IRB application, informed consent, and recruiting materialsEducates internal and external parties about new studies, providing guidance in understanding and implementing study protocolsPartner with Physicians and Advanced Practice Providers (APPs) for trial visits, including providing needed resources and trial details on an enduring basis throughout the trialEnsures that the well-being of research participants is safeguarded, and that participant’s rights are protectedParticipates in site initiation meetingConducts the informed consent process with potential research subjects in accordance with all regulatory, ethical and Institutional Review Board (IRB) requirementsConducts follow up visits per protocol, within defined parameters, and ensures thorough and accurate documentation using Good Documentation PracticesEnsures study participant safety and clinical trial protocol adherence using Good Clinical PracticesEnsures timely reporting of study required data that is thorough, complete, and accurate Participates in sponsor study initiation meetings As needed, provide clinical care, within guidelinesSupport trial implementation in a variety of clinical settings including ambulatory clinic, inpatient areas, and procedure areasRequiredEducation:Associate's Degree in NursingExperience:2 years clinical nursing experience2 years Clinical Research experience1-5 years research experience PreferredEducation:BSN degreeExperience:Cardiology, Diabetes, Acute Care, Critical Care, Cardiovascular lab, and electrophysiology experienceLicense/Registration/Certification:BLSClinical Research Coordinator Certification (CCRC) through Association of Clinical Research Professionals Certified Clinical Research Professional (CCRP) through Society of Clinical Research Associates Benefit OverviewFairview offers a generous benefit package including but not limited to medical, dental, vision plans, life insurance, short-term and long-term disability insurance, PTO and Sick and Safe Time, tuition reimbursement, retirement, early access to earned wages, and more!
Please follow this link foradditional information: https://www.fairview.org/careers/benefits/noncontract Compensation DisclaimerThe posted pay range is for a 40-hour workweek (1.0 FTE). The actual rate of pay offered within this range may depend on several factors, such as FTE, skills, knowledge, relevant education, experience, and market conditions. Additionally, our organization values pay equity and considers the internal equity of our team when making any offer.
Hiring at the maximum of the range is not typical. If your role is eligible for a sign-on bonus, the bonus program that is approved and in place at the time of offer, is what will be honored. EEO StatementEEO/Vet/Disabled: All qualified applicants will receive consideration without regard to any lawfully protected status