Clinical Research Coordinator II, Orthopaedic Surgery bei UT Southwestern Medical Center

%3Ch3%3E%3Cstrong%3EClinical Research Coordinator II - Orthopaedic Surgery Department%3C/strong%3E%3C/h3%3E%3Cp%3E%3Cstrong%3EWHY UT SOUTHWESTERN?%3C/strong%3E%3Cbr%3EWith over 75 years of excellence in Dallas-Fort Worth, Texas, UT Southwestern is committed to excellence, innovation, teamwork, and compassion. As a world-renowned medical and research center, we strive to provide the best possible care, resources, and benefits for our valued employees. Ranked as the number 1 hospital in Dallas-Fort Worth according to %3Ca target=%22_blank%22 rel=%22noopener noreferrer%22 href=%22https://www.utsouthwestern.edu/newsroom/articles/year-2022/july-us-news-best-hospital.html%22%3EU.S. News %26amp; World Report%3C/a%3E, we invest in you with opportunities for career growth and development to align with your future goals. Our highly competitive benefits package offers healthcare, PTO and paid holidays, on-site childcare, wage, merit increases and so much more. We invite you to be a part of the UT Southwestern team where you%27ll discover a culture of teamwork, professionalism, and a rewarding career!%26nbsp;%3Cbr%3E%3Cbr%3E%3Cstrong%3EJOB SUMMARY%3C/strong%3E%3Cbr%3EWorks under the direction of an Investigator(s) with limited supervision, to coordinate research projects. This position primarily performs patient/participant coordination, however, may conduct data management in smaller departments on as needed basis. Collects and ensures quality control of clinical or basic research data in support of multiple and/or complex research studies.%26nbsp;%3Cbr%3E%3Cbr%3E%26nbsp;%3C/p%3E%3Cp%3E%3Cstrong%3EBENEFITS%3C/strong%3E%3Cbr%3EUT Southwestern is proud to offer a competitive and comprehensive benefits package to eligible employees. Our benefits are designed to support your overall wellbeing, and include:%3C/p%3E%3Cul%3E%3Cli%3EPPO medical plan, available day one at no cost for full-time employee-only coverage%3C/li%3E%3Cli%3E100% coverage for preventive healthcare-no copay%3C/li%3E%3Cli%3EPaid Time Off, available day one%3C/li%3E%3Cli%3ERetirement Programs through the Teacher Retirement System of Texas (TRS)%3C/li%3E%3Cli%3EPaid Parental Leave Benefit%3C/li%3E%3Cli%3EWellness programs%3C/li%3E%3Cli%3ETuition Reimbursement%3C/li%3E%3Cli%3EPublic Service Loan Forgiveness (PSLF) Qualified Employer%3C/li%3E%3Cli%3E%3Ca target=%22_blank%22 rel=%22noopener noreferrer%22 href=%22http://jobs.utsouthwestern.edu/benefits/#top%22%3ELearn more about these and other UTSW employee benefits!%3C/a%3E%3C/li%3E%3C/ul%3E%3Cp%3E%3Cbr%3E%3Cbr%3E%3Cstrong%3EEXPERIENCE AND EDUCATION%3C/strong%3E%3Cbr%3E%3Cbr%3E%3Cstrong%3ERequired%3C/strong%3E%3C/p%3E%3Cul%3E%3Cli%3E%3Cstrong%3EEducation%3C/strong%3E%3Cbr%3EBachelor%27s Degree in medical or science related field%26nbsp;%3Cbr%3E%26nbsp;%3C/li%3E%3C/ul%3E%3Cul%3E%3Cli%3E%3Cstrong%3EExperience%3C/strong%3E%3Cbr%3E2 years years clinical research experience.%26nbsp;%3Cbr%3EMay consider additional years of experience or advanced degree in lieu of education or experience, respectively.%26nbsp;%3Cbr%3E%26nbsp;%3C/li%3E%3C/ul%3E%3Cp%3E%3Cstrong%3EPreferred%3C/strong%3E%3C/p%3E%3Cul%3E%3Cli%3E%3Cstrong%3ELicenses and Certifications%3C/strong%3E%3Cbr%3E(BLS) BASIC LIFE SUPPORT may be required based on research study protocols or affiliate location requirements.%26nbsp;%3Cbr%3E(CPRAED) CPR AED may be required based on research study protocols or affiliate location requirements.%26nbsp;%3Cbr%3EACRP or SOCRA certification a plus.%26nbsp;%3Cbr%3E%26nbsp;%3C/li%3E%3C/ul%3E%3Cp%3E%3Cbr%3E%3Cstrong%3EJOB DUTIES%3C/strong%3E%3C/p%3E%3Cul%3E%3Cli%3EDirectly interacts with clinical research participants, as required, for the research study (non-clinical and clinical procedures). Interacts via telephone, telehealth or in-person.%3C/li%3E%3Cli%3ECoordinates regulatory documentation for research studies that includes maintaining information to comply with industry standards, University policies, FDA requirements or other hospital policies.%3C/li%3E%3Cli%3ECoordinates and schedules procedures as per research study. A non-licensed coordinator may pend study order sets with oversight by PI.%3C/li%3E%3Cli%3EScreens, recruits, enrolls and follows subjects according to research protocol guidelines (non-clinical and clinical procedures). May also assist with the consent processes.%3C/li%3E%3Cli%3EMaintains and coordinates data collection information required for each study that may also include developing CRF%27s (case report form) or data collection tools.%3C/li%3E%3Cli%3EAssists in developing and implementing research studies, may include writing clinical research protocols.%3C/li%3E%3Cli%3EConducts research procedures according to the protocol with proper training and check offs to maintain scope of service.%3C/li%3E%3Cli%3EMay assist the PI on the fiscal management of the trial including budget preparation.%3C/li%3E%3Cli%3EMonitors patient safety by reviewing records and ensuring appropriate reporting per protocol and HRPP standards.%3C/li%3E%3Cli%3EMay perform research billing activities, as needed, based on size of department (including linking patient calendars).%3C/li%3E%3Cli%3ECoordinates data management and collection for national (larger/more complex) research studies or multiple research studies at a given time.%3C/li%3E%3Cli%3EServes as primary liaison/lead in preparing annual reports for federal, state, and or/or local agencies on assigned studies.%3C/li%3E%3Cli%3EPrepares protocols for Institutional Review Board (IRB) submission. May also submit amendments and continuing review documents.%3C/li%3E%3Cli%3EProvides in-service training to all study team members and communicates to involved groups.%3C/li%3E%3Cli%3EReviews research study protocols to ensure feasibility requirements of the study.%3C/li%3E%3Cli%3EAssists in developing website or other social media for marketing/recruiting based on assigned clinical research study.%3C/li%3E%3Cli%3EEnters data or assists in assembling data to enter in the assigned clinical trial management system, electronic medical record and/or other required data entry systems.%3C/li%3E%3Cli%3EMaintains required subject documentation for each study protocol.%3C/li%3E%3Cli%3EDuties performed may include one or more of the following core functions: a) Directly interacting with or caring for patients; b) Directly interacting with or caring for human-subjects research participants; c) Regularly maintaining, modifying, releasing or similarly affecting patient records (including patient financial records); or d) Regularly maintaining, modifying, releasing or similarly affecting human-subjects research records.%3C/li%3E%3Cli%3E%26nbsp;%3Col start=%2220%22%3E%3Cli%3EPerforms other duties as assigned.%3C/li%3E%3C/ol%3E%3C/li%3E%3C/ul%3E%3Cp%3E%3Cstrong%3ESECURITY AND EEO STATEMENT%3C/strong%3E%3Cbr%3E%3Cbr%3E%3Cstrong%3ESecurity%3C/strong%3E%3Cbr%3EThis position is security-sensitive and subject to Texas Education Code 51.215, which authorizes UT Southwestern to obtain criminal history record information.%3Cbr%3E%3Cbr%3E%3Cstrong%3EEEO%3C/strong%3E%3Cbr%3EUT Southwestern Medical Center is committed to an educational and working environment that provides equal opportunity to all members of the University community. As an equal opportunity employer, UT Southwestern prohibits unlawful discrimination, including discrimination on the basis of race, color, religion, national origin, sex, sexual orientation, gender identity, gender expression, age, disability, genetic information, citizenship status, or veteran status.%3Cbr%3E%26nbsp;%3C/p%3E Jetzt bewerben