Clinical Research Coordinator - Onsite - North Houston

Advanced Rheumatology of Houston • The Woodlands, TX

4d • Onsite

About The Position

ARH Research is seeking a motivated, detail-oriented, and patient-focused Clinical Research Coordinator (CRC) to join their team in The Woodlands, Texas. This full-time, on-site position involves conducting clinical trials focused on rheumatologic, autoimmune, and inflammatory conditions. The role offers the opportunity to work directly with patients, contribute to the development of new treatments, and be involved in the entire clinical trial process from startup to closeout. The CRC will take ownership of studies, work closely with experienced investigators, and interact directly with research participants.

Requirements

• 2+ years of Clinical Research Coordinator experience.
• RN/LVN must have clinical research experience.
• Strong knowledge of GCP, FDA regulations, informed consent, and clinical trial processes.
• Excellent organizational and time-management skills.
• Strong communication and documentation skills.
• Ability to independently manage multiple studies and competing priorities.
• Experience with EMRs, EDC systems, CTMS platforms, and clinical research technology.
• Ability to work on-site in The Woodlands, Texas.
• Must be legally authorized to work in the United States.

Nice To Haves

• Rheumatology, autoimmune, or inflammatory disease research experience.
• CCRC, CCRP, or similar certification.
• Nursing (RN & LVN) or other clinical experience.
• Bachelor’s degree preferred; however, candidates with a strong work history and medical office experience will also be considered.
• Phlebotomy and specimen-processing experience.
• Experience working with pharmaceutical sponsors and CROs.
• Spanish fluency.

Responsibilities

• Coordinate studies from startup through closeout.
• Identify, screen, recruit, and consent research participants.
• Conduct and coordinate study visits.
• Educate and support research participants throughout their study.
• Maintain accurate source documentation and study records.
• Manage visit schedules, windows, deadlines, and follow-up.
• Maintain regulatory files and essential study documents.
• Communicate with sponsors, CROs, monitors, investigators, and laboratories.
• Respond to data queries and maintain audit-ready documentation.
• Prepare for and assist with monitoring visits, audits, and inspections.
• Collect, process, package, and ship biological specimens.
• Work collaboratively with clinical and research staff to provide an exceptional participant experience.

Benefits

• Competitive compensation based on experience.
• Health, dental & vision insurance.
• 401(k) retirement plan.
• Scrub allowance.
• Paid time off.
• Paid holidays.
• Supportive, collaborative work environment.
• Professional development and career growth opportunities.
• Opportunity to work alongside experienced investigators and research professionals.
• Exposure to a variety of rheumatology and autoimmune clinical trials.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level