Apply for Job Job ID366500 LocationTwin Cities Job FamilyResearch Full/Part TimeFull-Time Regular/TemporaryRegular Job Code8351RC Employee ClassCivil Service Add to Favorite Jobs Email this Job About the Job Research Professional 1 or 2 Research Coordinator - Clinical Interventional/Therapeutic, DOQ Working Title: Clinical Research Coordinator Supervisor: Deb Mailand DESCRIPTION The Clinical Research Coordinator works under the direction of the Program Manager(s) and is responsible for day-to-day study activities including: participant screening and consent; study visits; data abstraction and entry; implementation of the study protocol; lab kit preparation and collection. The Clinical Research Coordinator will work across multiple study protocols, supporting various divisions in the Departments served (Department of Surgery and Department of Radiology). This position primarily supports the research conducted by the Department Radiology, specifically the division of Interventional Radiology. Projects include observational, data-driven outcomes research, as well as interventional research projects. This hybrid position will primarily work independently with day-to-day activities; and report to a Program Manager within the team. Given the need to consent in the clinics and coordinate biospecimens, the successful candidate should expect to be in the office routinely, 3+ days per week. The ability to work remotely exists and is dependent on work duties (i.e. data only days can be remote). A RP2RC will be expected to have more direct research experience, require less training to get started, work more independently, and be able to manage a larger workload independently. JOB DUTIES 1. Patient Screening, Recruitment, and Consent- 20% * Develop methods to identify potential participants such as via database searches and collaboration with internal and external partners. * Determine subject eligibility, and maintain compliance with protocol eligibility requirements. * Recruit potential subjects * Obtain or confirm subject's consent to participate in research. * Assess the subject's understanding of the research process, procedures and plan; implement and conduct subject and family education in response to identified needs. 2. Coordinate Participant Activities in Protocol- 30% * Assists PI, Program Manager and Research team with all activities relative to initiation of assigned clinical trials. * Assists Regulatory Specialist and Program Manager with drafting study-specific subject consent form documents and recruitment materials according to sponsor and University requirements. * Coordinate the implementation of the IRB approved protocol. * Develop and maintain accurate source documentation. * Develop methods to identify potential participants such as via database searches and collaboration with internal and external partners. Maintain accurate and complete study records and supplies. * Collect and ship specimens for research, laboratory, or clinical testing as required, often in repetitive and concise fashion to maintain integrity across all subject visits. * Monitor subject responses to protocol defined treatments/interventions, and schedule required visits and tests. * Evaluate laboratory and other findings to determine the presence of expected and unexpected subject reactions or outcomes * Assess, troubleshoot, and report problems with data collection or other research processes. * Under the supervision of the PI, report study/medical/test results for subjects and/or families and report significant findings to the appropriate study staff. * Correctly interpret and comply with applicable Federal Regulations, Good Clinical Practice, and local research regulatory requirements 3. Collect & Abstract Data- 25% * Abstract data from medical records and directly enter it into appropriate Research Database. * Perform study data collection and entry; collect enrollment and treatment data, using charts, correspondence, electronic medical recor s, and personal communications with other healthcare workers. * Complete and maintain essential source documentation, regulatory documents, and case-report forms (CRFs) * Receive and respond to data queries and monitoring action items as assigned 4. Communication and Training- 15% * Coordinate communication between all individuals involved in the research studies (PI, co-PI, sponsor, monitor, clinical staff, other members of the research team, and student employees) * Write routine correspondence for research projects including letters, memos, and instructional study forms * Interact with study monitors, department, University, and clinical staff to successfully carry out study requirements. * Provide ongoing and timely communication on the progress of the study to relevant parties * Assist in the training of local staff on the protocol. This includes, but is not limited to: assisting in creation of training materials, delivering education to research and clinical staff, and continually re-educating during the active phase of the active phase of the research project. 5. Other Duties as Assigned - 10% * Assist in REDCap eCRF, consent, or database build-outs and edits * Supports other special projects and program initiatives as directed. * Attends professional development and training sessions to ensure compliance with newest policies and procedures. * Serve as subject matter expert resource for others on the team with less experience The employer reserves the right to change or assign other duties to this position. Qualifications All required qualifications must be included in the application materials Required Qualifications for RP1RC: * BA/BS degree, or a combination of education and relevant work experience to equal at least four years. Required Qualifications for RP2RC: * BA/BS degree plus at least two years of relevant experience, or a combination of education and relevant work experience to equal at least six years. Required Qualifications for RP1RC and RP2RC: * Computer proficiency, and ability to navigate multiple software applications * Ability to work independently, make decisions, problem solve and prioritize the simultaneous management of multiple clinical studies. * Possess excellent communication skills; verbal and written. * Ability to work flexible work hours, including some early mornings, evenings, and weekends and on call as needed for studies. Typical hours will be Monday through Friday, but hours may vary based on study needs, which are based on case times. * Detail-oriented with exceptional organizational, planning and problem-solving skills * Ability to work independently, as part of a team, with changing priorities * Demonstrated ability to independently meet deadlines and prioritize assignments * Ability to interact with patient, staff, and research collaborators on a professional level Preferred Qualifications: * Familiarity with standard medical terminology, research terminology, laboratory environments, basic experimental techniques * Experience working in a clinical setting * Experience with human subjects research. * Certification: National certification in area... For full info follow application link. The University recognizes and values the importance of diversity and inclusion in enriching the employment experience of its employees and in supporting the academic mission. The University is committed to attracting and retaining employees with varying identities and backgrounds. The University of Minnesota provides equal access to and opportunity in its programs, facilities, and employment without regard to race, color, creed, religion, national origin, gender, age, marital status, disability, public assistance status, veteran status, sexual orientation, gender identity, or gender expression. To learn more about diversity at the U: http://diversity.umn.edu.