Research Enrollment Anlst

Job ID: 26012690Company: Baylor Scott & White HealthLocation: Dallas, Texas, United StatesJob Type: Full TimeHire Type: ProfessionalJob Level: Individual ContributorFLSA Status: Non-exemptShift: Day JobCategory: Allied HealthIndustry: HealthcarePosted Date: 2026-07-23About UsHere at Baylor Scott & White Health we promote the well-being of all individuals, families, and communities. Baylor Scott & White is the largest not-for-profit healthcare system in Texas that empowers you to live well.Our Core Values are:We serve faithfully by doing what's right with a joyful heart.We never settle by constantly striving for better.We are in it together by supporting one another and those we serve.We make an impact by taking initiative and delivering exceptional experience.BenefitsOur benefits are designed to help you live well no matter where you are on your journey. For full details on coverage and eligibility, visit the Baylor Scott & White Benefits Hub to explore our offerings, which may include:Immediate eligibility for health and welfare benefits401(k) savings plan with dollar-for-dollar match up to 5%Tuition ReimbursementPTO accrual beginning Day 1Note: Benefits may vary based upon position type and/or level.Job SummaryThe Research Enrollment Analyst, under general supervision, is accountable for enrolling participants in research projects, and developing and working on a self-directed research project that furthers the goals of the Investigators and Research Department.Essential Functions of the RoleCoordinates non-therapeutic (i.e. minimal risk, survey, chart review) clinical research protocols with direction from the principal investigator and/or supervisor in compliance with regulatory laws and institutional guidelines. May assist in complex studies with direction but does not have overall responsibility for these studies.Communicates with research participants via phone calls, mail-outs, and Internet to maintain the highest level of research participant retention possible.Maintains relationships with targeted research communities and investigators, patients, clinical managers, and supervisors.Screens potential research participants by reviewing inclusion and exclusion criteria.Enters new research participants in database and updates existing databases. Obtains and maintains consent forms. Documents the informed consent process.Ensures compliance with the internal policies and procedures, and standards of JCAHO, federal, state and local governments. Submits documentation to the Institutional Review Board (IRB) autonomously and follows the process to ensure approval.Attends research meetings, reads assigned literature, and makes presentations on projects at the request of the Principal Investigator (PI).Works with PIs to initiate research projects. Partners with the PI to establish and implement data collection procedures and protocols and assists with the preparation of documentation to ensure compliance with regulations and submissions required for current research projects. Assists in maintaining regulatory binders.Assists research physicians with study proposal development and helps to ensure that appropriate billing and charging mechanisms are in place for research charges.Assists research staff to ensure that applicable study supplies are received prior to study initiation and throughout the study period.Reviews data for completion and quality control and prepares data for further investigation. Works with biostatistical team as needed to create projects.Key Success FactorsPhlebotomy experience required and phlebotomy certification is preferredBiospecimen (e.g. urine, blood, stool, tissue) handling experience preferredExperience with Epic EMR, REDCap Database and/or Verily CTMS is preferredEnjoys predictable, process-oriented work and can maintain focus and quality when performing repetitive tasksAbility to independently troubleshoot routine challenges, resolve issues, and identify process improvementsProven written and oral communication skillsExcellent computer skills, including Microsoft Office, Excel, and PowerPointAbility to establish and maintain effective working relationships.Ability to manage time reactive projects in order to meet deadlinesAbility to effectively and efficiently perform data entries in large patient databases.Belonging StatementWe believe that all people should feel welcomed, valued and supported.QUALIFICATIONSEDUCATION - Associate's or 2 years of work experience above the minimum qualificationEXPERIENCE - Less than 1 Year of ExperienceSkillsphlebotomyinformed consent documentationregulatory complianceelectronic medical recordsdata entryjcaho complianceinclusion and exclusion screeningdatabase managementepic emrredcap databaseverily ctmsstudy protocol developmentquality controlmicrosoft officemicrosoft excelmicrosoft powerpointresearch participant retentionresearch proposal developmentbilling and charging mechanismsprocess improvementstakeholder communicationrelationship management