Senior Clinical Research Associate - Remote & Regional

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

Job summary

Syneos Health, Inc. is seeking an Experienced Clinical Research Associate to support regionally aligned trials across the United States. You will monitor sites, ensure compliance with ICH-GCP and study protocols, and collaborate with investigational teams to keep studies on track.

The role emphasizes remote work flexibility, timely data capture, and proactive issue escalation. You will partner with cross-functional groups to drive patient safety, data integrity, and regulatory readiness across

Responsibilities

• Performs site qualification, site initiation, interim monitoring, site management activities and close-out visits (performed on-site or remotely) ensuring regulatory, ICH-GCP and/or Good Pharmacoepidemiology Practice (GPP) and protocol compliance.
• Verifies the process of obtaining informed consent has been adequately performed and documented for each subject/patient, as required/appropriate.
• Per the Clinical Monitoring/Site Management Plan (CMP/SMP): Assesses site processes. Conducts Source Document Review of appropriate site source documents and medical records.
• Verifies required clinical data entered in the case report form (CRF) is accurate and complete.
• Applies query resolution techniques remotely and on site, and provides guidance to site staff as necessary, driving query resolution to closure within agreed timelines.
• Utilizes available hardware and software to support the effective conduct of the clinical study data review and capture.
• Verifies site compliance with electronic data capture requirements.
• May perform investigational product (IP) inventory, reconciliation and reviews storage and security.
• Verifies the IP has been dispensed and administered to subjects/patients according to the protocol.

Job description

Syneos Health, Inc. is seeking an Experienced Clinical Research Associate to support regionally aligned trials across the United States. You will monitor sites, ensure compliance with ICH-GCP and study protocols, and collaborate with investigational teams to keep studies on track.

The role emphasizes remote work flexibility, timely data capture, and proactive issue escalation. You will partner with cross-functional groups to drive patient safety, data integrity, and regulatory readiness across