Clinical Research Coordinator II: Drive Critical Trials

Evolution Research Group; Bellaire (TX); On-site; USD 34,000 - 37,000; Full time

Benefits offered by this job

Medical and dental coverage

401(k) match

Paid time off

Job summary

Evolution Research Group is seeking a Clinical Research Coordinator II for HDR First Surgical Hospital in Bellaire, TX. This full-time role handles study coordination, medication distribution, and regulatory documentation under PI guidance.

The CRC II will maintain accurate records, screen and enroll subjects, obtain informed consent, and ensure adherence to GCP, FDA regulations, and SOPs. Two to four years’ experience or certification is preferred.

Qualifications

• High School Diploma or equivalent; College degree preferred.
• Two to four years of experience OR certification as a Clinical Research Coordinator.
• Excellent communication with providers, coworkers, sponsors, and others.
• Knowledge of medical terminology to communicate with physician office and lab staff.
• Ability to act independently and make decisions within study protocols and regulatory requirements.

Responsibilities

• Coordinate overall clinical trial management under PI direction.
• Distribute study medication and instructions to subjects per protocol.
• Maintain accurate and confidential study records and regulatory documents.
• Ensure compliance with FDA regulations, GCP, and SOPs.
• Screen, enroll, and schedule visits with subjects; obtain informed consent.

Skills

Excellent communication skills

Medical terminology knowledge

Independent initiative

Regulatory knowledge (GCP/ICH)

Collaboration with study team

Education

High School Diploma

College degree preferred

Tools

Microsoft Word

Microsoft Excel

Study Manager

Job description

Evolution Research Group is seeking a Clinical Research Coordinator II for HDR First Surgical Hospital in Bellaire, TX. This full-time role handles study coordination, medication distribution, and regulatory documentation under PI guidance.

The CRC II will maintain accurate records, screen and enroll subjects, obtain informed consent, and ensure adherence to GCP, FDA regulations, and SOPs. Two to four years’ experience or certification is preferred.