Remote CRA: Site Monitoring & Compliance

Syneos Health, Inc.; Nevada; Remote; USD 75,000 - 130,000; Full time

Benefits offered by this job

Company car or car allowance

Health benefits (medical, dental, VSP)

401(k) with company match

Employee stock purchase plan

Bonuses based on performance

Flexible PTO and sick time

Job summary

Syneos Health, Inc. seeks an Experienced Clinical Research Associate regionally aligned across the US. The role focuses on site qualification, initiation, monitoring and close-out visits to ensure ICH-GCP compliance.

You will verify consent, data integrity and support IP handling while coordinating with sponsor teams. Travel up to 75% is expected, with remote site management as needed. You'll work within a dynamic global CRO setting, contributing to audit readiness, TMF accuracy, and site

Qualifications

• Bachelor's degree or RN in related field or equivalent experience.
• Knowledge of Good Clinical Practice/ICH Guidelines and regulatory requirements.
• Excellent computer, communication and interpersonal skills.

Responsibilities

• Performs site qualification/initiation, monitoring and close-out visits (on-site or remote) with regulatory/ICH-GCP compliance.
• Verifies informed consent procedures and protects subject confidentiality and data integrity.
• Conducts source data review, CRF data verification and remote query resolution.
• Manages IP inventory, labeling, storage, and reconciliation per protocol.
• Maintains ISF/TMF quality and aids in audit readiness and site training.
• Supports recruitment/retention strategies and tracks observations and actions.
• Collaborates with sponsor and country staff; participates in meetings and training.

Skills

Bachelor's degree or RN

GCP knowledge

Computer skills

Communication skills

Travel up to 75%

Education

Bachelor's degree or RN

Job description

Syneos Health, Inc. seeks an Experienced Clinical Research Associate regionally aligned across the US. The role focuses on site qualification, initiation, monitoring and close-out visits to ensure ICH-GCP compliance.

You will verify consent, data integrity and support IP handling while coordinating with sponsor teams. Travel up to 75% is expected, with remote site management as needed. You'll work within a dynamic global CRO setting, contributing to audit readiness, TMF accuracy, and site