Clinical Research Coordinator I

Location: Richardson, Texas, USA; full-time onsite role

Company

A global testing, inspection, and certification company operating offices and laboratories worldwide.

What you will do

• Coordinate assigned clinical studies as lead coordinator and execute follow-up visits.
• Set up and conduct studies according to protocols, SOPs, applicable regulations, and GCP guidelines.
• Perform document review, data entry, clinical data collection, instrumentation duties, and test-material preparation.
• Prepare and maintain study documentation, including protocol amendments, case report forms, EDC records, and study-specific materials.
• Coordinate subject scheduling, monitor panelist compliance, and resolve issues and queries from Quality Assurance and Statistics teams.
• Coordinate study staff, meetings, budgets, and other tasks assigned by the Clinic Manager or Supervisor.

Requirements

• Associate degree, or at least two years of relevant experience with a GED or high school diploma.
• Basic understanding of clinical research and the ability to learn and perform clinical study duties.
• Language, mathematical, reasoning, and computer skills.
• Ability to manage and coordinate multiple projects in a fast-paced professional environment.
• Ability to address panelist issues, arrange study work, and make decisions as a study leader.

Culture & Benefits

• Work is performed in a highly professional clinical research environment.
• Responsibilities are carried out in accordance with quality, regulatory, and GCP standards.
• Reasonable accommodations are available for qualified individuals with disabilities.
• Equal employment opportunity is provided across job classifications.