Remote Clinical Research Associate – Full-Service Trials

Syneos Health, Inc.; Washington (District of Columbia); Hybrid; USD 65,000 - 90,000; Full time

Benefits offered by this job

Company car or car/allowance

Health benefits (Medical, Dental, VIs)

401k match

Employee Stock Purchase Plan

Commissions/bonus eligibility

Flexible PTO and sick time

Job summary

Syneos Health is seeking a Clinical Research Associate for a Full-Service role that supports remote and on-site site activities in the U.S. The role emphasizes regulatory compliance, data integrity, and collaboration with investigators to ensure high-quality trial execution.

The CRA will verify informed consent, manage source data, and maintain trial documentation while traveling up to 75% as needed. This position enables contributions across sponsor partnerships and global studies.

Qualifications

• Bachelor’s degree or RN in a related field or equivalent
• Knowledge of GCP/ICH guidelines and regulatory requirements
• Strong computer skills and ability to adopt new technologies
• Excellent communication, presentation and interpersonal skills
• Willingness to travel up to 75% US-wide

Responsibilities

• Performs site qualification, initiation, monitoring, and close-out visits (onsite or remote) ensuring ICH-GCP/regulatory compliance.
• Verifies informed consent processes and protects subject confidentiality.
• Conducts Source Document Review and CRF data validation; guides site staff to resolution.
• Manages IP inventory, labeling, storage per protocol, and dispensing verification.
• Prepares for and participates in Investigator Meetings and sponsor meetings; supports audit readiness.

Skills

Bachelor’s degree or RN

GCP/ICH knowledge

Computer skills

Communication skills

Travel readiness

Education

Bachelor’s degree or RN

Job description

Syneos Health is seeking a Clinical Research Associate for a Full-Service role that supports remote and on-site site activities in the U.S. The role emphasizes regulatory compliance, data integrity, and collaboration with investigators to ensure high-quality trial execution.

The CRA will verify informed consent, manage source data, and maintain trial documentation while traveling up to 75% as needed. This position enables contributions across sponsor partnerships and global studies.