On‑Site Clinical Research Coordinator — Data & Study Ops

ALS Limited; Irving (TX); On-site; USD 28,000 - 36,000; Full time

Job summary

ALS Limited in Irving, Texas is seeking a Clinical Research Coordinator to oversee planning, coordination, and execution of clinical studies. The role involves preparing study materials, obtaining informed consent, and ensuring compliant data collection under GCP guidelines.

Qualified candidates typically hold a Bachelor’s degree in life sciences, with 1–2 years of clinical experience and relevant certifications.

Qualifications

• Bachelor’s degree in life sciences preferred or related field.
• Current certificates for Human Protections, Good Clinical Practices, Bloodborne Pathogens preferred.
• 1–2 years’ experience in clinical industry is desirable.

Responsibilities

• Coordinate and support planning, initiation, and day-to-day execution of clinical research studies.
• Prepare materials, informed consent forms, screening materials, and study logs per protocols.
• Explain procedures to participants and obtain informed consent in collaboration with the study team.
• Maintain study areas, prepare supplies, and ensure proper handling and disposal of study materials.
• Monitor participant responses, record adverse events, and document data accurately.
• Operate study equipment, maintain data files, and ensure proper storage of study records.
• Collaborate with investigators and management to communicate progress and deliver sponsor reports.

Skills

Computer skills

Clinical experience

Education

Bachelor's degree

Job description

ALS Limited in Irving, Texas is seeking a Clinical Research Coordinator to oversee planning, coordination, and execution of clinical studies. The role involves preparing study materials, obtaining informed consent, and ensuring compliant data collection under GCP guidelines.

Qualified candidates typically hold a Bachelor’s degree in life sciences, with 1–2 years of clinical experience and relevant certifications.