Clinical Trial Pre-Screening Coordinator II

Alliance Clinical Network; Lewisville (TX); On-site; USD 55,000 - 75,000; Full time

Job summary

Alliance Clinical Network in Lewisville, TX seeks a Pre-Screen Coordinator II to coordinate site screening schedules, manage pre-screening operations, and oversee patient eligibility assessments.

The role requires reviewing protocols and informed consent, conducting pre-screen visits, and maintaining accurate records while ensuring compliance with FDA regulations and GCP. Excellent communication and organizational skills are essential in a fast-paced research environment.

Qualifications

• Associate or higher degree preferred.
• 2 years of experience in running research protocols preferred.
• Knowledge of FDA regulations and GCP preferred.
• Strong verbal and written communication skills required.

Responsibilities

• Review protocols and informed consent for eligibility and recruitment.
• Conduct pre-screen visits and assessments.
• Maintain records including contact info, birth dates, and eligibility data.
• Explain study procedures, risks, benefits, and follow-up to potential participants.

Skills

Analytical thinking

Attention to detail

Communication skills

Multitasking

Education

Associate’s degree

Bachelor’s degree

Master’s degree

Job description

Alliance Clinical Network in Lewisville, TX seeks a Pre-Screen Coordinator II to coordinate site screening schedules, manage pre-screening operations, and oversee patient eligibility assessments.

The role requires reviewing protocols and informed consent, conducting pre-screen visits, and maintaining accurate records while ensuring compliance with FDA regulations and GCP. Excellent communication and organizational skills are essential in a fast-paced research environment.