Remote CRA II – Site Management & Trials

Syneos Health, Inc.; Illinois; On-site; USD 70,000 - 95,000; Full time

Benefits offered by this job

Company car/Car allowance

Medical, Dental, Vision benefits

401k match

Employee Stock Purchase Plan

Bonuses/variable compensation

Paid time off (PTO)

Job summary

Syneos Health, Inc. is seeking an Experienced Clinical Research Associate to work regionally across the US. You will perform site qualification, initiation, interim monitoring, and close-out visits, ensuring ICH-GCP and regulatory compliance, while protecting patient safety and data integrity.

This role involves significant travel and collaboration with sponsor teams. As part of the Clinical Development model, you’ll support site management, data review, IP inventory, and audit readiness.

Qualifications

• GCP/ICH knowledge and regulatory requirements lighter responsibilities.
• Good computer skills and adaptability to new technologies.
• Excellent communication, presentation and interpersonal skills.
• Willingness to travel up to 75% regularly.

Responsibilities

• Performs site qualification, initiation, interim monitoring, and close-out visits (on-site or remote) with regulatory, ICH-GCP and GPP compliance.
• Verifies informed consent procedures and protects patient confidentiality; assesses safety and data integrity.
• Conducts source document review, data entry checks, and supports query resolution to closure.
• Manages IP inventory, labeling, and storage per protocol; ensures regulatory compliance.
• Maintains ISF/TMF accuracy and archiving in accordance with guidelines.
• Documents activities via letters, trip reports, logs, and SOP-compliant records; supports recruitment and tracking.

Skills

GCP/ICH knowledge

Strong communication

Computer proficiency

Travel up to 75%

Education

Bachelor's degree or RN in related field

Job description

Syneos Health, Inc. is seeking an Experienced Clinical Research Associate to work regionally across the US. You will perform site qualification, initiation, interim monitoring, and close-out visits, ensuring ICH-GCP and regulatory compliance, while protecting patient safety and data integrity.

This role involves significant travel and collaboration with sponsor teams. As part of the Clinical Development model, you’ll support site management, data review, IP inventory, and audit readiness.