Remote Clinical Research Associate — Site Monitoring Expert

Syneos Health, Inc.; Indiana; On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Company car / car allowance

Health, dental, and vision benefits

401k with employer match

Employee Stock Purchase Plan

Commissions/bonus based on performance

Flexible PTO and sick time

Job summary

Syneos Health, Inc. is seeking an Experienced Clinical Research Associate (CRA II) regionally aligned across the US.

The role focuses on site qualification, initiation, monitoring, data integrity, and close-out visits, with extensive travel and strong regulatory knowledge. You will collaborate with site staff and sponsor teams to ensure protocol compliance and high-quality data, participating in investigator meetings and audit readiness.

Qualifications

• Bachelor's degree or RN required.
• Knowledge of Good Clinical Practice/ICH Guidelines and regulatory requirements.
• Excellent communication, presentation and interpersonal skills.
• Ability to travel up to 75% regularly.
• Must embrace new technologies and have solid computer skills.

Responsibilities

• Performs site qualification, initiation, monitoring, and close-out visits (on-site/remote).
• Verifies informed consent documentation and patient safety considerations.
• Reviews ISF and TMF, ensures archiving per local guidelines.
• Maintains site regulatory data, supports IP inventory and handling per protocol.
• Supports site staff training, audit readiness, and escalation of issues.
• Acts as liaison with study sites and sponsor meetings; supports recruitment and data quality.

Skills

GCP knowledge

Computer skills

Communication skills

Travel readiness

Education

Bachelor's degree or RN (related field)

Job description

Syneos Health, Inc. is seeking an Experienced Clinical Research Associate (CRA II) regionally aligned across the US.

The role focuses on site qualification, initiation, monitoring, data integrity, and close-out visits, with extensive travel and strong regulatory knowledge. You will collaborate with site staff and sponsor teams to ensure protocol compliance and high-quality data, participating in investigator meetings and audit readiness.