Clinical Research Coordinator — Data-Driven Trials

ALS; Irving (TX); On-site; USD 25,000 - 33,000; Full time

Job summary

ALS is seeking a Clinical Research Coordinator in Irving, TX. The role involves planning, coordinating, and executing clinical studies under PI supervision per GCP guidelines. You will manage documentation, consent, and study materials while ensuring compliance and data integrity.

The position requires a 4-year degree and life sciences background, with 1–2 years of clinical experience preferred. Salary is hourly at $21, with duties spanning site operations, data collection, and participant

Qualifications

• Bachelor's degree from a 4 year university.
• BS/BA in life sciences preferred.
• Current certificate for: Human Protections, Good Clinical Practices, Bloodborne Pathogens
• Computer skills required.
• 1–2 years’ experience in clinical industry experience (substitute for BS or BA).

Responsibilities

• Coordinate and support planning, initiation, implementation, and day-to-day execution of clinical research studies in accordance with protocols, sponsor requirements, SOPs, and GCP guidelines.
• Prepare, organize, and maintain study materials and documentation (informed consent, screening, medical history, source documents, study calendars, diaries, sign-in sheets).
• Explain procedures to participants, obtain informed consent, and verify eligibility with recruitment team.
• Prepare study areas, patches, materials, dilutions, and supplies for study conduct and logs.
• Handle test articles and materials per protocol, safety procedures, and guidelines.
• Conduct daily clinical study activities to support workflow and subject throughput while ensuring compliance.
• Monitor subjects’ responses, document observations, and record adverse events in study records.
• Operate study instruments, collect data, download images, and store files properly.
• Update and maintain study data tables, databases, and tracking tools for oversight and reporting.
• Collaborate with investigators and management to communicate progress and support protocol/report production.
• Provide front-desk and administrative support including participant greeting and attendance.

Skills

Computer skills

Education

Bachelor's degree (4-year)

BS/BA in life sciences

Job description

ALS is seeking a Clinical Research Coordinator in Irving, TX. The role involves planning, coordinating, and executing clinical studies under PI supervision per GCP guidelines. You will manage documentation, consent, and study materials while ensuring compliance and data integrity.

The position requires a 4-year degree and life sciences background, with 1–2 years of clinical experience preferred. Salary is hourly at $21, with duties spanning site operations, data collection, and participant