Regional Clinical Research Associate - Remote/On-Site

Syneos Health, Inc.; Washington; Remote; USD 70,000 - 110,000; Full time

Benefits offered by this job

Health benefits (medical, dental, VIs)

Company car or car allowance

401k with company match

Employee Stock Purchase Plan

Bonus eligibility

Flexible paid time off

Job summary

Syneos Health is seeking an Experienced Clinical Research Associate to support regionally aligned monitoring across the United States. The role involves site qualification, initiation, monitoring, and close-out visits, conducted on-site or remotely, with up to 75% travel.

You will verify consent, protect patient safety, review ISF/TMF, and support data integrity. You will collaborate with sponsor teams, ensure regulatory compliance, and participate in Investigator Meetings.

Qualifications

• Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements.
• Excellent communication, presentation and interpersonal skills.
• Ability to manage required travel of up to 75% on a regular basis.

Responsibilities

• Performs site qualification, initiation, monitoring and close-out visits (on-site or remotely) ensuring regulatory and protocol compliance.
• Verifies informed consent processes and protects patient confidentiality.
• Reviews site documents, enters data, and supports recruitment and retention efforts.
• Ensures site and project team are trained and compliant with applicable requirements.
• Participates in investigator meetings and sponsor meetings; prepares for audits and follow-up actions.

Skills

GCP/ICH Knowledge

Communication Skills

Interpersonal Skills

Travel Readiness

Tech Savvy

Education

Bachelor's degree or RN

Job description

Syneos Health is seeking an Experienced Clinical Research Associate to support regionally aligned monitoring across the United States. The role involves site qualification, initiation, monitoring, and close-out visits, conducted on-site or remotely, with up to 75% travel.

You will verify consent, protect patient safety, review ISF/TMF, and support data integrity. You will collaborate with sponsor teams, ensure regulatory compliance, and participate in Investigator Meetings.