Clinical Research Coordinator — Study Data & Patient Impact

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

Job summary

ALS is seeking a Clinical Research Coordinator to plan, coordinate, and execute clinical studies in Irving, Texas. You will handle informed consent, screening, and documentation, while ensuring adherence to protocols and GCP guidelines.

The role involves daily study activities, data management, and collaboration with investigators and sponsors. Requirements include a 4-year degree (life sciences preferred), relevant certifications (GCP, Human Protections, Bloodborne Pathogens), computer skills,

Qualifications

• Bachelor’s degree from a 4 year university.
• Bachelor of Science or Arts degree in life sciences preferred.
• Certificates, licenses, and registrations 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 and GCP guidelines.
• Prepare, organize, and maintain study materials and documentation (informed consent, screening materials, source documents, etc.).
• Explain procedures to research participants, obtain informed consent, ensure eligibility criteria are met with Recruitment Department.
• Prepare study areas, patches, materials, and supplies for study conduct.
• Receive, log, prepare, and dispose of test articles per protocol and safety procedures.
• Coordinate daily clinical study activities to support efficient workflow and subject throughput.
• Monitor subjects’ responses, record adverse events and study data in records.
• Operate study instruments, download and maintain study data and images, ensure proper shutdown.
• Maintain study data tables, databases, and tracking tools for oversight.
• Communicate progress with investigators, project managers, and management; support protocol/doc deliverables.
• Provide front-desk and clerical support; maintain organized study files and archives.
• Order, stock, and maintain laboratory and study supplies; ensure readiness of study areas.
• Perform opening/closing procedures and housekeeping for study areas.
• Support senior clinical staff and other duties as assigned.

Skills

Computer skills

Education

Bachelor’s degree from a 4 year university

Bachelor of Science or Arts in life sciences preferred

Certificates for Human Protections

Good Clinical Practices certificate

Bloodborne Pathogens certificate

1–2 years’ clinical industry experience

Job description

ALS is seeking a Clinical Research Coordinator to plan, coordinate, and execute clinical studies in Irving, Texas. You will handle informed consent, screening, and documentation, while ensuring adherence to protocols and GCP guidelines.

The role involves daily study activities, data management, and collaboration with investigators and sponsors. Requirements include a 4-year degree (life sciences preferred), relevant certifications (GCP, Human Protections, Bloodborne Pathogens), computer skills,