Remote Clinical Research Associate - Regional Monitoring

Syneos Health, Inc.; Bridgeport (CT); On-site; USD 75,000 - 105,000; Full time

Benefits offered by this job

Company car or car allowance

Health benefits: Medical, Dental and V

401k

Employee Stock Purchase Plan

Bonus based on performance

Flexible PTO and sick time

Job summary

Syneos Health, Inc. is seeking an Experienced Clinical Research Associate to support regionally aligned monitoring across the US. The role emphasizes site qualification, initiation, monitoring, data accuracy, and regulatory compliance within ICH-GCP guidelines.

The position requires travel up to 75% and combines field work with collaboration across sponsor teams to ensure high-quality data and patient safety.

Qualifications

• Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements.
• Must demonstrate good computer skills and be able to embrace new technologies.
• Excellent communication, presentation and interpersonal skills.
• Ability to manage required travel of up to 75% on a regular basis.

Responsibilities

• Performs site qualification, site initiation, interim monitoring, site management activities and close-out visits (on-site or remote).
• Verifies informed consent procedures and protects patient confidentiality.
• Reviews ISF and TMF; ensures archiving per local guidelines.
• Maintains data quality in CRFs and supports source data verification.
• Supports recruitment, retention and site training; tracks observations and actions.

Skills

Good computer skills

Excellent communication

Interpersonal skills

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 support regionally aligned monitoring across the US. The role emphasizes site qualification, initiation, monitoring, data accuracy, and regulatory compliance within ICH-GCP guidelines.

The position requires travel up to 75% and combines field work with collaboration across sponsor teams to ensure high-quality data and patient safety.