Remote Clinical Research Associate – Site Monitoring Expert

Syneos Health, Inc.; Helena (MT); On-site; USD 65,000 - 95,000; Full time

Benefits offered by this job

Health benefits

401k match

Stock Purchase Plan

Bonuses

PTO

Job summary

Syneos Health, Inc. is seeking an Experienced Clinical Research Associate to support regionally aligned activities across the US. The role involves site qualification, initiation, monitoring, and close-out visits with adherence to ICH-GCP and protocol requirements.

Candidates should travel up to 75% and collaborate across sponsor and site teams to ensure data integrity and regulatory compliance. This position emphasizes strong communication, site management, and the ability to adapt to varying

Qualifications

• Bachelor's degree in life sciences or nursing or equivalent.
• Knowledge of Good Clinical Practice/ICH Guidelines and other regulatory requirements.
• Strong communication and interpersonal skills; able to adapt to travel up to 75%.
• Experience with site monitoring, ISF/TMF relationships, and data quality processes.

Responsibilities

• Performs site qualification, initiation, interim monitoring, site management and close-out visits (on-site or remote).
• Verifies informed consent procedures and protects subject confidentiality.
• Reviews CRF data, performs query resolution, and ensures data integrity in tracking systems.
• Manages IP inventory, storage, and labeling per protocol.
• Maintains ISF accuracy and ensures archiving per guidelines.
• Coordinates site communications, timelines, and risk management.
• Prepares for Investigator Meetings and sponsor meetings; supports audit readiness.

Skills

Excellent communication

Project coordination

ICH-GCP knowledge

Travel readiness

Education

Bachelor's degree in life sciences or nursing

Tools

EDC systems

MS Office

Job description

Syneos Health, Inc. is seeking an Experienced Clinical Research Associate to support regionally aligned activities across the US. The role involves site qualification, initiation, monitoring, and close-out visits with adherence to ICH-GCP and protocol requirements.

Candidates should travel up to 75% and collaborate across sponsor and site teams to ensure data integrity and regulatory compliance. This position emphasizes strong communication, site management, and the ability to adapt to varying