Remote Clinical Research Associate – Site Monitoring

Syneos Health, Inc.; Florida; On-site; USD 80,000 - 120,000; Full time

Job summary

Syneos Health is seeking an Experienced Clinical Research Associate (CRA) to support site monitoring activities across the United States. The role requires handling site qualification, initiation, monitoring visits and data verification in alignment with ICH-GCP guidelines.

The CRA will work regionally, collaborating with cross-functional teams to ensure protocol compliance, data integrity and timeliness of trial deliverables. Travel up to 75% may be required depending on study needs.

Qualifications

• Bachelor’s degree or RN in a related field.
• Knowledge of Good Clinical Practice/ICH Guidelines.
• Good computer skills and ability to learn new technologies.
• Excellent communication, presentation and interpersonal skills.
• Ability to travel up to 75% regularly.
• US-only privacy notice—employment may involve sharing data with sites as required.

Responsibilities

• Performs site qualification, initiation, interim monitoring, site management and close-out visits (on-site or remotely).
• Verifies informed consent and protects subject confidentiality.
• Reviews CRF data quality, performs query resolution and supports data integrity.
• Manages IP inventory and ensures protocol-compliant dispensing/reconciliation.
• Maintains ISF alignment with TMF; ensures archiving per guidelines.
• Supports site recruitment, retention and tracking of study observations.

Skills

ICH-GCP Knowledge

Site Monitoring

Communication Skills

Travel Readiness

Team Collaboration

Education

Bachelor's degree or RN

Job description

Syneos Health is seeking an Experienced Clinical Research Associate (CRA) to support site monitoring activities across the United States. The role requires handling site qualification, initiation, monitoring visits and data verification in alignment with ICH-GCP guidelines.

The CRA will work regionally, collaborating with cross-functional teams to ensure protocol compliance, data integrity and timeliness of trial deliverables. Travel up to 75% may be required depending on study needs.