Clinical Trial Pre-Screen Coordinator II

Alliance Clinical Network; San Diego (CA); On-site; USD 55,000 - 75,000; Full time

Job summary

Alliance Clinical Network is seeking a Pre-Screen Coordinator II in San Diego to coordinate site screening schedules, oversee pre-screening operations, and assess participant eligibility. The role also involves maintaining contact logs and coordinating with investigators to meet screening and randomization goals.

The candidate will review protocols and informed consent, conduct pre-screen visits, maintain records, explain study procedures, and ensure compliance with GCP and study guidelines.

Qualifications

• Associate’s degree in healthcare or related field preferred.
• Bachelor’s degree in biology, life sciences, public health, or related field preferred.
• A master’s degree is a plus.

Responsibilities

• Coordinate and oversee site screening schedules and pre-screening operations.
• Oversee patient eligibility assessments and QA to ensure regulatory compliance.
• Review protocols and informed consent documents for eligibility and recruitment.
• Explain study procedures, risks, benefits, and follow-up to potential participants.
• Maintain detailed records of candidate information and screening results.
• Support development of HCP network to drive referrals and maintain partnerships.

Skills

Analytic reasoning

Problem solving

Attention to detail

Communication skills

Multitasking

Education

Associate degree in healthcare

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

Master’s degree is a plus

Job description

Alliance Clinical Network is seeking a Pre-Screen Coordinator II in San Diego to coordinate site screening schedules, oversee pre-screening operations, and assess participant eligibility. The role also involves maintaining contact logs and coordinating with investigators to meet screening and randomization goals.

The candidate will review protocols and informed consent, conduct pre-screen visits, maintain records, explain study procedures, and ensure compliance with GCP and study guidelines.