Clinical Research Coordinator – Houston, Texas Leading Clinical Research Organisation

Green Life Science; Houston (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

Green Life Science is seeking two Clinical Research Coordinators to join our Houston, TX site. You will collaborate with the Principal Investigator and Site Director to coordinate, manage, and implement clinical trials in compliance with FDA regulations and GCP guidelines.

The role requires a high school diploma (college degree preferred) and CRC experience, with proficiency in Word, Excel, and study management tools.

Qualifications

• Former CRC experience required.
• High School Diploma required; college degree preferred.
• Knowledge of medical terminology and regulatory requirements (GCP/ICH).
• Strong communication skills - interpersonal, written, and verbal.
• Proficiency in Word, Excel, and clinical research applications (e.g. Study Manager).
• Ability to work independently, exercise sound judgement, and adapt in a dynamic environment.

Responsibilities

• Review and analyse study protocols prior to study start-up.
• Manage studies in collaboration with the Principal Investigator, Site Director, and Recruitment Manager.
• Screen and enrol subjects; schedule and conduct study visits.
• Obtain informed consent from study volunteers.
• Maintain accurate, organised, and complete study records.
• Enter data via paper or electronic data capture systems.
• Track and report adverse events per protocol requirements.
• Liaise with sponsors, IRBs, labs, and regulatory organisations.
• Support SOP development and study close-out procedures.

Skills

Medical terminology

Regulatory knowledge

Communication skills

Word & Excel

Clinical research apps

Education

High School Diploma

College degree preferred

Tools

Study Manager

Job description

Clinical Research Coordinator - Houston, Texas

Location: Houston, Texas (TX)

Headcount: 2 Openings

About The Role

We are partnered with a leading clinical research organisation dedicated to delivering high-quality Phase I-IV clinical trial execution. Our client has completed over 5,000 trials with deep expertise in neuroscience, clinical pharmacology, psychiatry, neurology, acute pain, and metabolic disorders, with affiliate sites across the U.S.

Why join them? Our client offers a supportive culture, meaningful work, and the opportunity to contribute to cutting-edge research alongside industry leaders - plus competitive benefits including medical and dental coverage, a matching 401(k), and paid time off.

Our client is seeking 2 Clinical Research Coordinators. The successful candidates will be responsible for the coordination, management, and implementation of clinical trials. Working under the direction of the Principal Investigator and Site Director, you will complete study-related procedures, manage documentation, and ensure compliance with FDA regulations, GCP guidelines, and company SOPs.

Key Responsibilities

• Review and analyse study protocols prior to study start-up
• Manage studies in collaboration with the Principal Investigator, Site Director, and Recruitment Manager
• Screen and enrol subjects; schedule and conduct study visits
• Obtain informed consent from study volunteers
• Maintain accurate, organised, and complete study records
• Enter data via paper or electronic data capture systems
• Track and report adverse events per protocol requirements
• Liaise with sponsors, IRBs, labs, and regulatory organisations
• Support SOP development and study close-out procedures

What We’re Looking For

• Former CRC experience required
• High School Diploma required; college degree preferred
• Knowledge of medical terminology and regulatory requirements (GCP/ICH guidelines)
• Strong communication skills - interpersonal, written, and verbal
• Proficiency in Word, Excel, and clinical research applications (e.g. Study Manager)
• Ability to work independently, exercise sound judgement, and adapt in a dynamic environment