Clinical Research Coordinator II — Drive Cutting-Edge Trials

Evolution Research Group; Bellaire (TX); On-site; USD 55,000 - 75,000; Full time

Benefits offered by this job

Medical and dental coverage

401(k) matching

Paid time off

Job summary

Evolution Research Group is seeking a Clinical Research Coordinator II (CRC-II) for full-time work at our Bellaire, TX site. You will coordinate trial activities, manage regulatory documentation, and ensure accurate data capture under the direction of the Principal Investigator and Site Director.

This role supports multiple studies per FDA and GCP standards. The CRC-II collaborates with investigators, nurses, and sponsors to screen and enroll subjects, obtain informed consent, and maintain

Qualifications

• Strong communication skills, both written and verbal, with healthcare teams.
• Knowledge of medical terminology to communicate with clinicians and labs.
• Ability to act independently and make decisions within study protocols and regulations.

Responsibilities

• Coordinate and manage clinical trials per protocol and SOPs.
• Screen, enroll subjects and schedule visits with investigators.
• Obtain informed consent from potential volunteers and maintain records.
• Ensure regulatory documentation, IRB communications, and drug dispensing logs are complete.
• Report adverse events per protocol and track study progress with sponsors.

Skills

Communication skills

Medical terminology

Independent initiative

Team collaboration

Regulatory knowledge

Education

High School Diploma

College degree preferred

CRC certification

Tools

Word

Excel

Study Manager

Job description

Evolution Research Group is seeking a Clinical Research Coordinator II (CRC-II) for full-time work at our Bellaire, TX site. You will coordinate trial activities, manage regulatory documentation, and ensure accurate data capture under the direction of the Principal Investigator and Site Director.

This role supports multiple studies per FDA and GCP standards. The CRC-II collaborates with investigators, nurses, and sponsors to screen and enroll subjects, obtain informed consent, and maintain