Senior Clinical Research Associate – Global Site Management

Syneos Health/ inVentiv Health Commercial LLC; Westerville (OH); On-site; USD 70,000 - 110,000; Full time

Benefits offered by this job

Company car or car allowance

Job summary

Syneos Health is seeking an Experienced Clinical Research Associate to support sponsor-dedicated trials. The role covers site qualification, initiation, interim monitoring, and close-out visits, with on-site or remote work as needed.

You will verify informed consent, monitor data integrity, and guide site staff to resolve issues in line with ICH-GCP and CMP/SMP. The role requires a Bachelor’s or RN and the ability to travel up to 75% regularly.

Qualifications

• Bachelor's degree or RN required or equivalent
• Knowledge of Good Clinical Practice/ICH Guidelines
• Excellent communication, presentation and interpersonal skills
• Ability to travel up to 75% regularly

Responsibilities

• Performs site qualification/initiation, interim monitoring, site management and close-out visits (on-site or remote) with regulatory and protocol compliance.
• Verifies informed consent processes and protects subject confidentiality; assesses safety and data integrity factors.
• Performs SDV/CRF data review, applies query resolution remotely or on-site, and drives timely issue resolution.
• Manages IP inventory, storage and labeling per protocol; ensures proper release and return.
• Maintains ISF/TMF accuracy and archiving; supports recruitment, retention and data tracking.

Skills

Excellent communication

Travel up to 75%

Site qualification/initiation/monitor

ICH-GCP knowledge

Computer literacy

Education

Bachelor's degree or RN in related field

Tools

Microsoft Office

Job description

Syneos Health is seeking an Experienced Clinical Research Associate to support sponsor-dedicated trials. The role covers site qualification, initiation, interim monitoring, and close-out visits, with on-site or remote work as needed.

You will verify informed consent, monitor data integrity, and guide site staff to resolve issues in line with ICH-GCP and CMP/SMP. The role requires a Bachelor’s or RN and the ability to travel up to 75% regularly.