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Clinical Research Coordinator

Advanced Rheumatology of Houston

The Woodlands, Texas

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JOB DETAILS
SALARY
$50,000–$85,000
SKILLS
Autoimmune Disease, Certified Clinical Research Coordinator (CCRC), Clinical Information Systems, Clinical Nursing, Clinical Practices/Protocols, Clinical Research, Clinical Support, Clinical Trial, Clinical Trial Management, Communication Skills, Conduct Studies, Contract Research Organization (CRO), Detail Oriented, Disease Investigation, Documentation, Electronic Medical Records, FDA Requirements, GCP (Good Clinical Practices), Healthcare Quality, IRB/IEC (Institutional Review Board/Independent Ethics Committee), Maintain Compliance, Organizational Skills, Patient Care, Patient Education, Patient Follow-up, Regulations, Regulatory Requirements, Regulatory Submissions, Research Protocols, Rheumatology, Spanish Language, Startup, Team Player, Time Management
LOCATION
The Woodlands, Texas
POSTED
6 days ago
Experienced Clinical Research Coordinator (Rheumatology)
Location: The Woodlands, Texas
Job Type: Full-Time

We are a growing private rheumatology practice in The Woodlands seeking an experienced Clinical Research Coordinator (CRC) to support and manage clinical trials focused on autoimmune and inflammatory conditions. This role is ideal for a detail-oriented professional who thrives in a fast-paced clinical environment and is passionate about advancing patient care through research.

Key Responsibilities:
  • Coordinate and manage all aspects of clinical trials from startup through closeout.
  • Screen, recruit, and consent eligible patients for research studies.
  • Ensure compliance with study protocols, GCP guidelines, and regulatory requirements.
  • Collect, document, and maintain accurate study data and source documentation.
  • Serve as liaison between investigators, sponsors, CROs, and regulatory bodies.
  • Schedule and conduct study visits, including patient education and follow-up.
  • Maintain IRB submissions, regulatory binders, and study documentation.
  • Assist with monitoring visits, audits, and data queries.

Qualifications:
  • Minimum 2–3 years of clinical research coordination experience required.
  • Experience in rheumatology or autoimmune disease studies strongly preferred.
  • Strong understanding of GCP, FDA regulations, and clinical trial processes.
  • Excellent organizational, communication, and patient interaction skills.
  • Ability to manage multiple studies and deadlines independently.
  • Proficiency in EMR systems and clinical trial management software..
  • Certification (CCRC, CCRP, or equivalent) preferred but not required.
  • Nursing/Clinical background a plus.
  • Fluency in Spanish is a plus.

What We Offer:
  • Competitive salary based on experience.
  • Health, dental, and vision insurance.
  • Paid time off and holidays.
  • Supportive team environment in a reputable private practice.
  • Opportunity to contribute to meaningful advancements in rheumatologic care.

Join a dedicated team committed to improving patient outcomes through high-quality clinical research in a collaborative and patient-centered setting.

About the Company

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Advanced Rheumatology of Houston