Clinical Research Associate I

@ Syneos Health

Overview

Clinical Research Associate I at Syneos Health is part of a fully integrated biopharmaceutical solutions team committed to accelerating customer success by translating clinical, medical affairs, and commercial insights into actionable outcomes.

What You'll Do

You will perform site qualification, initiation, monitoring, management, and close-out visits (both on-site and remote) while ensuring regulatory, ICH-GCP, and protocol compliance. You will:

• Evaluate site performance and recommend site-specific actions
• Ensure proper documentation of informed consent and patient confidentiality
• Conduct Source Document Reviews and verify clinical data accuracy
• Monitor investigational product handling, storage, and dispensing
• Document site activities via reports and logs

Additional Responsibilities

For Real World Late Phase studies, you may act as Site Management Associate I, supporting site identification, data collection, and collaboration with sponsor affiliates. You will also be involved in training site staff, preparing for Investigator Meetings, and ensuring audit readiness.

Qualifications

A Bachelor’s degree or RN in a related field is required along with knowledge of ICH-GCP and regulatory guidelines. Excellent computer, communication, and interpersonal skills are required. Be prepared to travel up to 75% regularly.

Why Syneos Health?

Join a global leader with 29,000 employees across 110 countries, committed to career development, training, comprehensive benefits, and a Total Self culture where you can be your authentic self.

Key Skills/Competency

• Clinical monitoring
• Regulatory compliance
• Site management
• Data review
• Informed consent
• GCP
• Audit readiness
• Patient safety
• Risk assessment
• Communication