Remote Clinical Research Associate: Site Monitoring

Syneos Health, Inc.; Minnesota; Hybrid; USD 75,000 - 105,000; Full time

Benefits offered by this job

Health benefits

401k match

Employee Stock Purchase Plan

Bonus program

Car allowance

Job summary

Syneos Health, Inc. in the United States is seeking a Clinical Research Associate - Full-Service to monitor sites remotely or on-site as needed. You will perform site qualification, initiation, monitoring, and close-out activities to ensure GCP compliance across trials.The role emphasizes collaboration with sponsor teams, data integrity, and audit readiness, with up to 75% travel and a supportive culture that emphasizes development and total rewards.

Qualifications

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

Responsibilities

• Performs site qualification, initiation, monitoring, and close-out visits ensuring regulatory compliance.
• Verifies informed consent documentation and protects subject confidentiality.
• Reviews ISF and TMF, and supports audit readiness and data integrity.
• Manages site-level activities and communicates to ensure project objectives and timelines.
• Prepares for Investigator Meetings and sponsor meetings.
• Provides guidance to site staff on SOPs and regulatory requirements.

Skills

GCP/ICH knowledge

Communication

Travel up to 75%

Computer literacy

Education

Bachelor’s degree or RN

Job description

Syneos Health, Inc. in the United States is seeking a Clinical Research Associate - Full-Service to monitor sites remotely or on-site as needed. You will perform site qualification, initiation, monitoring, and close-out activities to ensure GCP compliance across trials.The role emphasizes collaboration with sponsor teams, data integrity, and audit readiness, with up to 75% travel and a supportive culture that emphasizes development and total rewards.