Senior Clinical Research Associate - Remote/Global Trials

Syneos Health, Inc.; Carson City (NV); On-site; USD 70,000 - 110,000; Full time

Job summary

Syneos Health is seeking an Experienced Clinical Research Associate to support regionally across the US. The role involves site qualification, initiation, monitoring, and close-out visits, on-site or remote, with strict adherence to ICH-GCP and study SOPs.

Strong communication and travel readiness are essential. The successful candidate will verify informed consent, perform source data review, and ensure data integrity while coordinating with site staff and project teams.

Qualifications

• Bachelor's degree or RN in a related field or equivalent combination of education, training and experience.
• 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.
• US ONLY: Deployment to sites needing access information per privacy notice; compliance required.

Responsibilities

• Performs site qualification, initiation, interim monitoring, management, and close-out visits; on-site or remote with regulatory compliance.
• Verifies informed consent process and protects subject confidentiality; assess safety and data integrity.
• Conducts source data review, CRF data accuracy, and query resolution; supports IP handling per SOPs.
• Maintains ISF/TMF accuracy; ensures archiving of essential documents per guidelines.
• Communicates project scope, budgets and timelines; adapts to changing priorities to meet targets.
• Acts as liaison with site personnel; ensures training and compliance of site team members.

Skills

Excellent communication

Presentation skills

Interpersonal skills

Computer skills

Willingness to travel

Education

Bachelor's degree or RN

Job description

Syneos Health is seeking an Experienced Clinical Research Associate to support regionally across the US. The role involves site qualification, initiation, monitoring, and close-out visits, on-site or remote, with strict adherence to ICH-GCP and study SOPs.

Strong communication and travel readiness are essential. The successful candidate will verify informed consent, perform source data review, and ensure data integrity while coordinating with site staff and project teams.