Clinical Trials Pre-Screen Coordinator II

Alliance Clinical; San Diego (CA); On-site; USD 30,000 - 33,000; Full time

Job summary

Alliance Clinical seeks a Pre-Screen Coordinator II in San Diego, CA to coordinate and oversee site screening schedules and pre-screening operations. You will manage patient eligibility assessments, consent review, and documentation to ensure protocol compliance.

The role requires attention to detail, strong communication, and the ability to multitask in a fast-paced clinical research environment. Prior clinical trial experience is preferred.

Qualifications

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

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, risks and benefits to participants before entry.
• Create and maintain detailed records of candidate information and visit notes.
• Coordinate site screening schedules and workflow to meet targets.
• Monitor QA findings and ensure compliance across visits.

Skills

Attention to detail

Communication skills

Analytical reasoning

Multitasking

Education

Associate’s degree in healthcare or related field

Bachelor’s degree in biology/life sciences/public health or related field

Master’s degree is a plus

Job description

Alliance Clinical seeks a Pre-Screen Coordinator II in San Diego, CA to coordinate and oversee site screening schedules and pre-screening operations. You will manage patient eligibility assessments, consent review, and documentation to ensure protocol compliance.

The role requires attention to detail, strong communication, and the ability to multitask in a fast-paced clinical research environment. Prior clinical trial experience is preferred.