Clinical Research Coordinator

ALS Global • Irving, TX

10d

About The Position

The Clinical Research Coordinator plans, coordinates, and executes clinical research studies, including collecting and managing clinical trial data. The role supports safety and efficacy studies under the supervision of the Principal Investigator and in accordance with approved protocols, company standard operating procedures, and current Good Clinical Practice guidelines. The coordinator performs assigned responsibilities to support compliant, accurate, and efficient study execution. Duties may vary according to the assigned site, study type, protocol requirements, testing methodology, instrumentation, and operational needs.

Requirements

• Bachelor’s degree from a four-year university.
• Computer skills.
• One to two years of clinical industry experience may be substituted for a bachelor’s degree.

Nice To Haves

• Bachelor of Science or Bachelor of Arts degree in life sciences.
• Current certificates in Human Protections, Good Clinical Practices, and Bloodborne Pathogens.

Responsibilities

• Coordinate and support the planning, initiation, implementation, and day-to-day execution of clinical research studies according to study protocols, sponsor requirements, company procedures, and Good Clinical Practice guidelines.
• Prepare, organize, and maintain study materials and documentation, including consent forms, screening materials, source documents, study calendars, diaries, sign-in sheets, and administrative notebooks.
• Explain study procedures to participants, obtain informed consent, and help confirm eligibility and entrance criteria with the Recruitment Department and study team.
• Prepare study areas, patch booths, test materials, patches, dilutions, supplies, and related logs.
• Receive, log, weigh, prepare, fill, refill, rinse, and dispose of test articles and related materials according to protocol and safety requirements.
• Coordinate daily study activities, scheduling, workflow, and participant throughput while maintaining compliance.
• Monitor participant responses, assign or enter protocol-defined scoring, document observations, and record adverse events and other study data.
• Operate study instruments and equipment, support data collection, maintain study images and electronic files, and ensure equipment is shut down and stored properly.
• Prepare and maintain study data tables, subject databases, logs, and tracking tools.
• Collaborate with investigators, project managers, clinical management, and internal departments on study progress, status updates, protocols, reports, and sponsor deliverables.
• Provide participant-facing and administrative support, including greeting participants, recording attendance, and performing routine clerical tasks.
• Maintain complete, current, organized, and inspection-ready study files and administrative records.
• Order, stock, restock, and maintain laboratory, clinic, and study supplies.
• Perform routine facility and study-area opening and closing procedures, including securing entrances, managing alarms, and preparing work areas for study activities.
• Perform cleaning, disposal, and housekeeping tasks associated with study execution and maintain related records and logs.
• Support senior clinical research staff and management and perform other related duties as assigned.

Benefits

• Programs and opportunities to develop new skills and build a diverse career.
• Reasonable adjustments to support candidates throughout the recruitment process are available upon request.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level