Clinical Research Coordinator

About Medrasa Clinical Research

Medrasa Clinical Research is a clinical trial site in Wylie, TX focused on delivering high-quality data across metabolic, renal, and pulmonary studies. We partner with leading pharmaceutical sponsors and CROs to execute complex, procedure-driven trials with strong patient retention and operational excellence.

Position Summary

We are hiring an experienced Clinical Research Coordinator (CRC) to independently manage clinical trials from startup through closeout. This role is ideal for candidates with prior CRC experience who are comfortable working directly with sponsors, managing patients, and ensuring full protocol and regulatory compliance.

Key Responsibilities

• Serve as primary coordinator for assigned clinical trials
• Manage study startup, maintenance, and closeout activities
• Coordinate patient visits, scheduling, and follow-ups
• Conduct patient screening, recruitment, and enrollment
• Perform clinical procedures and patient assessments per protocol
• Maintain accurate source documentation and EDC data entry
• Ensure ICH-GCP compliance and protocol adherence
• Communicate with sponsors, CROs, and monitors
• Prepare for and support monitoring visits, audits, and inspections
• Resolve data queries, deviations, and study-related issues
• Collaborate with the Principal Investigator (PI) on eligibility, safety, and oversight

Required Qualifications

• 2–3+ years of Clinical Research Coordinator (CRC) experience
• Strong knowledge of ICH-GCP, FDA regulations, and clinical trial operations
• Experience with patient recruitment, screening, and consent
• Experience with EDC systems and source documentation
• Ability to manage multiple studies and deadlines independently
• Strong communication and organizational skills

Preferred Qualifications

• Experience with complex or procedure-heavy trials
• Phlebotomy and clinical procedures experience
• Experience with sponsor/CRO interactions and monitoring visits
• Bilingual (Spanish)

Why Join Medrasa

• Work at a high-enrolling, sponsor-preferred site
• Exposure to complex clinical trials and advanced protocols
• Direct interaction with top pharmaceutical sponsors and CROs
• Growth opportunities into senior and leadership roles
• Collaborative, high-performance team environment

Job Type: Full-time

Pay: $23.00 - $26.00 per hour

Benefits:

• Flexible schedule
• Paid time off

Work Location: In person