Remote Clinical Research Associate – Site Management

Syneos Health, Inc.; Springfield (IL); On-site; USD 85,000 - 130,000; Full time

Benefits offered by this job

Company car or car allowance

Health benefits (Medical, Dental, and

401k match

Employee Stock Purchase Plan

Paid time off and sick leave

Job summary

Syneos Health is seeking an Experienced Clinical Research Associate regionally aligned across the United States. The role focuses on site qualification, initiation, monitoring, data integrity and regulatory compliance to support the Clinical Development program.

You will work on-site and remotely as needed, with up to 75% travel to sites. Responsibilities include investigator meetings, ensuring protocol adherence, and maintaining audit-ready documentation in line with CMP/SMP requirements.

Qualifications

• Bachelor's degree or RN in a related field; equivalent combination of education, training and experience.
• Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements.
• Excellent communication, presentation and interpersonal skills.

Responsibilities

• Performs site qualification, initiation, interim monitoring, site management activities and close-out visits (on-site or remote).
• Verifies informed consent and protects patient confidentiality.
• Maintains ISF/TMF accuracy and supports audit readiness.
• Coordinates IP inventory, labeling, and storage per protocol.
• Supports subject recruitment, data entry and reconciliation within timelines.
• Manages site-level activities and communications to meet project objectives.
• Attends investigator meetings and sponsor meetings as required.
• Prepares for audits and ensures compliance with SOPs.

Skills

Excellent communication

Interpersonal skills

Travel up to 75%

Computer skills

Education

Bachelor's degree or RN in a related field

Job description

Syneos Health is seeking an Experienced Clinical Research Associate regionally aligned across the United States. The role focuses on site qualification, initiation, monitoring, data integrity and regulatory compliance to support the Clinical Development program.

You will work on-site and remotely as needed, with up to 75% travel to sites. Responsibilities include investigator meetings, ensuring protocol adherence, and maintaining audit-ready documentation in line with CMP/SMP requirements.