Clinical Research Coord 1

Job ID: 26012689Company: Baylor Scott & White HealthLocation: Red Oak, Texas, United StatesJob Type: Full TimeHire Type: ProfessionalJob Level: Individual ContributorFLSA Status: ExemptShift: Day JobCategory: Allied HealthIndustry: HealthcarePosted Date: 2026-09-18About UsHere at Baylor Scott & White Health we promote the well-being of all individuals, families, and communities. Baylor Scott and 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 Clinical Research Coordinator 1 helps Principal Investigators (PI) with clinical trials. This includes all trial phases, from pre-study to closure, following federal, state, and Institutional guidelines. This position will learn to assist on complex studies and seek guidance from senior roles when needed. *This position is primarily based at the Irving location.Essential Functions of the RoleImplements various protocols for assigned research projects with appropriate departments. Interacts with PIs, clinical managers, and supervisors.Creates, facilitates, or executes various project workflows based on clinical trial protocol needs. Examples include providing in-service education for healthcare professionals and working with Pharmacy to ensure smooth project flow.Ensures appropriate billing mechanisms are in place for research charges. Requires familiarity with research study budgets. Provides feedback on budgets for new clinical trials.Performs research subject informed consent and entry into appropriate research studies ensuring that all inclusion and exclusion criteria are met.Partners and coordinates with regulatory compliance. Prepares Institutional Review Board (IRB) materials for protocol amendments. Submits Investigational New Drug (IND) Safety forms. Ensures all study documents are complete. Retains records per federal, state, and institutional standards.Obtains knowledge of departmental functions through reading literature, attending workshops, seminars and conferences and participating in professional organizations.Conducts and coordinates study-monitoring visits. Conducts audits and quality checks to ensure research studies are accurate, consistent, and have integrity.Key Success FactorsResearch certification or other certifications per specialty area preferred.Proven written and oral communication skills.Exceptional computer skills, including Microsoft Office.Ability to manage time reactive projects in order to meet deadlines.Exceptional ability to establish and maintain effective working relationships.Belonging StatementWe believe that all people should feel welcomed, valued and supported.QUALIFICATIONSEDUCATION - Bachelor's or 4 years of work experience above the minimum qualificationEXPERIENCE - Less than 1 Year of ExperienceSkillsclinical trial coordinationinformed consent administrationregulatory complianceinstitutional review board (irb) materialsinvestigational drug (ind) safety formsstudy monitoringquality auditsresearch subject entryresearch subject informed consentproject workflow managementbudget feedbackresearch subject retentionmicrosoft officeresearch certificationin-service educationpharmacy collaborationwritten communicationoral communicationrelationship management