Clinical Research Coordinator: Drive Trials + Benefits

Green Life Science; Houston (TX); Sur place; USD 55 000 - 75 000; Plein temps

Avantages offerts par ce poste

Medical and dental coverage

401(k) matching

Paid time off

Résumé du poste

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.

Responsabilités

• 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.

Connaissances

Medical terminology

Regulatory knowledge

Communication skills

Word & Excel

Clinical research apps

Formation

High School Diploma

College degree preferred

Outils

Study Manager

Description du poste

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.