Remote-Eligible Clinical Research Associate

Syneos Health, Inc.; Miami (FL); On-site; USD 70,000 - 110,000; Full time

Benefits offered by this job

Company car

Health benefits

401k

Stock purchase plan

Bonus potential

PTO

Job summary

Syneos Health seeks an Experienced Clinical Research Associate to support regionally across the US. The role involves site qualification, initiation, monitoring, and close-out visits with a focus on regulatory compliance and patient safety.

You will work with site staff to ensure data integrity, perform source data reviews, and assist with audit readiness while traveling up to 75% across the United States. A strong background in GCP/ICH and excellent communication are essential.

Qualifications

• Bachelor's degree or RN in a related field plus experience in clinical monitoring.
• Knowledge of Good Clinical Practice/ICH Guidelines and applicable regulatory requirements.
• Able to use computer systems effectively and adapt to new technologies.
• Excellent communication, presentation and interpersonal skills; travel up to 75% regularly.

Responsibilities

• Performs site qualification, initiation, interim monitoring, and close-out visits (onsite/remote) with regulatory and protocol adherence.
• Verifies informed consent and maintains subject confidentiality; monitors safety and data integrity.
• Reviews ISF/TMF, conducts source data reviews, and guides site staff to timely query resolution.
• Manages IP inventory and ensures proper labeling, storage, and dispensing per protocol.
• Maintains audit readiness and supports site training; documents activities per SOPs and plans.
• Collaborates with sponsor/global teams; supports recruitment, retention, and tracking of actions.

Skills

ICH-GCP knowledge

Excellent communication

Travel up to 75%

Site qualification monitoring

Education

Bachelor's degree or RN

Job description

Syneos Health seeks an Experienced Clinical Research Associate to support regionally across the US. The role involves site qualification, initiation, monitoring, and close-out visits with a focus on regulatory compliance and patient safety.

You will work with site staff to ensure data integrity, perform source data reviews, and assist with audit readiness while traveling up to 75% across the United States. A strong background in GCP/ICH and excellent communication are essential.