Clinical Research Coordinator — Drive Impactful Studies

Als; Irving (TX); On-site; USD 37,000 - 50,000; Full time

Job summary

ALS is seeking a Clinical Research Coordinator to plan, coordinate, and execute clinical studies, including data collection and management.

Under supervision of the Principal Investigator, you will ensure compliance with GCP guidelines and SOPs and support study documentation and participant interactions.

This role requires a BS in life sciences and 1–2 years of clinical industry experience, with an hourly rate indicated.

Qualifications

• Bachelor’s degree from a 4 year university; life sciences preferred.
• Current certificates for Human Protections, Good Clinical Practices, Bloodborne Pathogens are preferred.

Responsibilities

• Coordinate and support planning, initiation, implementation, and day-to-day execution of clinical research studies in accordance with protocols and GCP guidelines.
• Prepare and maintain study materials and documentation (informed consent forms, screening materials, medical history forms, source documents, study logs).
• Explain procedures to participants and obtain informed consent; verify eligibility with the study team.
• Prepare areas and materials for study conduct, ensure proper preparation of equipment and supplies.
• Handle test articles and related materials per protocol and safety procedures.
• Monitor subjects and record adverse events; ensure accurate data entry in study records.
• Operate study instruments, collect data, and maintain study images/files.
• Maintain study data tables, logs, and tracking tools for oversight and reporting.

Education

Bachelor's degree in life sciences

Job description

ALS is seeking a Clinical Research Coordinator to plan, coordinate, and execute clinical studies, including data collection and management.

Under supervision of the Principal Investigator, you will ensure compliance with GCP guidelines and SOPs and support study documentation and participant interactions.

This role requires a BS in life sciences and 1–2 years of clinical industry experience, with an hourly rate indicated.