Clinical Research Coordinator — Drive Trials & Data

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

Job summary

ALS is seeking a Clinical Research Support role in Texas. The duties include coordinating the planning, initiation, and day-to-day execution of clinical studies, ensuring compliance with study protocols and GCP guidelines.

The position requires a 4-year degree, preferred life sciences degree, and certificates in Human Protections/GCP/Bloodborne Pathogens, along with 1–2 years of clinical industry experience. Computer skills are required.

Qualifications

• Bachelor's degree is required.
• BS/BA in life sciences preferred.
• Current certificates for Human Protections, Good Clinical Practices, Bloodborne Pathogens preferred.

Responsibilities

• Coordinate and support planning, initiation, implementation, and day-to-day execution of clinical research studies per protocols and GCP guidelines.
• Prepare, organize, and maintain study materials and documentation including informed consent forms and study calendars.
• Explain study procedures to participants and obtain informed consent with recruitment team collaboration.

Skills

Computer skills

Education

Bachelor's degree from a 4 year university

BS/BA in life sciences preferred

Certifications for Human Protections, GCP, Bloodborne Pathogens

Job description

ALS is seeking a Clinical Research Support role in Texas. The duties include coordinating the planning, initiation, and day-to-day execution of clinical studies, ensuring compliance with study protocols and GCP guidelines.

The position requires a 4-year degree, preferred life sciences degree, and certificates in Human Protections/GCP/Bloodborne Pathogens, along with 1–2 years of clinical industry experience. Computer skills are required.