Clinical Research Coordinator - Houston Trials & Compliance

Green Life Science; Houston (TX); On-site; USD 52,000 - 78,000; Full time

Benefits offered by this job

Medical and dental coverage

Matching 401(k)

Paid time off

Job summary

Green Life Science is seeking two Clinical Research Coordinators in Houston, TX to manage and implement clinical trials under the direction of the Principal Investigator and Site Director.

You will perform study-related procedures, maintain documentation, and ensure FDA/GCP compliance while collaborating with sponsors, labs, and IRBs. A strong emphasis on data integrity and patient safety guides daily responsibilities.

Qualifications

• Strong communication skills across interpersonal, written, and verbal channels.
• Ability to work independently and exercise good judgment in dynamic environments.
• Knowledge of FDA regulations and GCP/ICH guidelines.

Responsibilities

• Review and analyze study protocols prior to start-up.
• Coordinate trials with Principal Investigator, Site Director, and Recruitment Manager.
• Screen and enroll subjects; schedule and conduct visits.

Skills

Strong communication

Independent work

Regulatory knowledge

Education

High School Diploma

College degree preferred

Tools

Word

Excel

Study Manager

Job description

Green Life Science is seeking two Clinical Research Coordinators in Houston, TX to manage and implement clinical trials under the direction of the Principal Investigator and Site Director.

You will perform study-related procedures, maintain documentation, and ensure FDA/GCP compliance while collaborating with sponsors, labs, and IRBs. A strong emphasis on data integrity and patient safety guides daily responsibilities.