Clinical Research Coord 1

Baylor Scott & White Health

Plano, TXFull-timePosted Apr 20, 2026

Behavioral Health Market Context

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Benefits

Our benefits are designed to help you live well no matter where you are on your journeyImmediate eligibility for health and welfare benefits401(k) savings plan with dollar-for-dollar match up to 5%Tuition ReimbursementPTO accrual beginning Day 12 more items(s)

Qualifications

  • 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
  • EDUCATION - Bachelor's or 4 years of work experience above the minimum qualification
  • EXPERIENCE - Less than 1 Year of Experience
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Responsibilities

  • The 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
  • Implements 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
  • 16 more items(s)


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