Clinical Research Coordinator I - Trial Ops & Compliance

Baylor Scott & White Health

Plano (TX)

On-site

USD 52,000 - 70,000

Full time

7 days ago
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Benefits offered by this job

Health benefits
401(k) matching
Tuition Reimbursement
PTO Day 1

Job summary

Baylor Scott & White Health is seeking a Clinical Research Coordinator I in Plano, TX to support Principal Investigators across all trial phases in compliance with federal, state, and institutional guidelines. You will learn to assist on complex studies and collaborate with senior staff for guidance.

The role emphasizes documentation, budgeting, and coordinating with regulatory teams to ensure study integrity and patient safety.

Qualifications

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

Responsibilities

  • Implements protocols for assigned research projects with appropriate departments.
  • Creates, facilitates, or executes project workflows per protocol needs.
  • Ensures appropriate billing mechanisms for research charges.
  • Performs research subject informed consent and entry into studies.
  • Coordinates with regulatory compliance; prepares IRB materials and IND safety forms.
  • Learns departmental functions via literature and trainings; participates in professional organizations.
  • Conducts study-monitoring visits and quality checks for data integrity.

Skills

Research coordination
Written communication
Microsoft Office
Budget awareness
IRB familiarity

Education

Bachelor's degree or 4 years of work experience above the minimum qualification

Tools

IRB processes

Job description

Baylor Scott & White Health is seeking a Clinical Research Coordinator I in Plano, TX to support Principal Investigators across all trial phases in compliance with federal, state, and institutional guidelines. You will learn to assist on complex studies and collaborate with senior staff for guidance.

The role emphasizes documentation, budgeting, and coordinating with regulatory teams to ensure study integrity and patient safety.

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