Clinical Research Coordinator: End-to-End Trials

Baylor Scott & White Health

Dallas (TX)

On-site

USD 52,000 - 68,000

Full time

7 days ago
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Benefits offered by this job

Immediate health and welfare benefits
401(k) with 5% match
Tuition Reimbursement
PTO from Day 1

Job summary

Baylor Scott & White Health in Irving, TX seeks a Clinical Research Coordinator I to support Principal Investigators across all trial phases, from pre-study to closure, following federal and institutional guidelines.

This role primarily operates from the Irving location, coordinating protocols, budgets, informed consent, and regulatory materials while collaborating with study teams to ensure quality and compliance.

Qualifications

  • Bachelor's degree or 4 years of work experience above the minimum qualification.
  • Less than 1 year of experience.

Responsibilities

  • Implements protocols for assigned research projects with appropriate departments.
  • Creates, facilitates, or executes project workflows and educates healthcare professionals.
  • Ensures billing mechanisms for research charges and assists with budgeting for trials.
  • Performs research subject informed consent and enrollment ensuring inclusion/exclusion criteria.
  • Coordinates with regulatory compliance; prepares IRB materials and Regulatory documents.
  • Keeps knowledge of departmental functions via literature, workshops and professional groups.
  • Coordinates study-monitoring visits and conducts audits to ensure integrity.

Skills

Research coordination
Communication
Time management
Budgeting
Team collaboration

Education

Bachelor's degree or 4 years experience

Tools

Microsoft Office

Job description

Baylor Scott & White Health in Irving, TX seeks a Clinical Research Coordinator I to support Principal Investigators across all trial phases, from pre-study to closure, following federal and institutional guidelines.

This role primarily operates from the Irving location, coordinating protocols, budgets, informed consent, and regulatory materials while collaborating with study teams to ensure quality and compliance.

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