Clinical Trials Pre-Screen Coordinator II

ALLIANCE CLINICAL LLC; Lewisville (TX); On-site; USD 42,000 - 60,000; Full time

Job summary

Alliance Clinical Network in Lewisville, TX is seeking a Pre-Screen Coordinator II to coordinate and oversee site screening schedules, manage pre-screening operations, and assess participant eligibility for multiple clinical studies.

You will review protocols and consent documents, conduct pre-screen visits, maintain records, and ensure compliance with FDA regulations and GCP. Strong organizational and communication skills are essential.

Qualifications

• 2 years of experience running research protocols.
• 2 years of experience with FDA regulations and GCP.
• Strong organizational and interpersonal skills.
• Excellent verbal and written communication skills.

Responsibilities

• Review and break down protocols and informed consent documents for patient eligibility and recruitment.
• Conduct pre-screen visits and assessments.
• Explain the study procedures and risks, benefits, and follow-up to participants.
• Create and maintain detailed records of candidate information.
• Oversee site screening schedules and ensure compliance and audit readiness.

Skills

FDA regulations

GCP

Analytical reasoning

Attention to detail

Communication skills

Multitasking

Education

Associate’s degree in healthcare or related field

Bachelor’s degree in biology/life sciences/public health

Master’s degree (plus)

Job description

Alliance Clinical Network in Lewisville, TX is seeking a Pre-Screen Coordinator II to coordinate and oversee site screening schedules, manage pre-screening operations, and assess participant eligibility for multiple clinical studies.

You will review protocols and consent documents, conduct pre-screen visits, maintain records, and ensure compliance with FDA regulations and GCP. Strong organizational and communication skills are essential.