Senior Clinical Research Associate – Remote & Travel‑Ready

Syneos Health, Inc.; Charleston (WV); Remote; USD 85,000 - 125,000; Full time

Benefits offered by this job

Company car or car allowance

Health benefits

401k / retirement savings

Job summary

Syneos Health is seeking an Experienced Clinical Research Associate (CRA) regionally aligned across the US. The role focuses on site qualification, initiation, monitoring and close-out visits, ensuring ICH-GCP and protocol compliance, with remote options and travel up to 75%.

Strong GCP knowledge, data integrity and site management skills are required. Responsibilities include data capture, IP handling, ISF/TMF reconciliation, audit readiness, and collaboration with sponsor teams.

Qualifications

• Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements
• Must demonstrate good computer skills and be able to embrace new technologies
• 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, management and close-out visits ensuring ICH-GCP, GPP and protocol compliance.
• Verifies informed consent procedures and protects subject confidentiality; assesses safety and data integrity risks.
• Per CMP/SMP: assesses site processes, performs source data review, ensures CRF accuracy and query resolution.
• May handle IP inventory, reconciliation, and storage security; ensures IP dispensing per protocol.
• Reviews ISF for accuracy and reconciles with TMF; ensures archiving per guidelines.
• Documents activities and supports recruitment/retention; enters data to tracking systems.
• Manages scope, budgets, and timelines; adapts to changing priorities to meet goals.
• Acts as liaison with site personnel or with Central Monitoring Associate; ensures training and compliance.
• Prepares for Investigator Meetings and sponsor meetings; participates in global meetings and training.
• Guides audit readiness and supports audit preparation and follow-up actions.
• Maintains knowledge of ICH/GCP; for Real World Late Phase SMA II site lifecycle support.

Job description

Syneos Health is seeking an Experienced Clinical Research Associate (CRA) regionally aligned across the US. The role focuses on site qualification, initiation, monitoring and close-out visits, ensuring ICH-GCP and protocol compliance, with remote options and travel up to 75%.

Strong GCP knowledge, data integrity and site management skills are required. Responsibilities include data capture, IP handling, ISF/TMF reconciliation, audit readiness, and collaboration with sponsor teams.