Remote Clinical Research Associate – Site Management

Syneos Health, Inc.; Boston (MA); Remote; USD 85,000 - 130,000; Full time

Job summary

Syneos Health is seeking an Experienced Clinical Research Associate (CRA) regionally aligned across the US. The CRA will monitor sites, ensure regulatory compliance, and collaborate with cross-functional teams to accelerate trial delivery.

This role requires up to 75% travel, strong knowledge of ICH-GCP, data integrity, and excellent communication. On-site or remote monitoring, ISF/TMF coordination, and audit readiness are part of daily responsibilities.

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.

Responsibilities

• Performs site qualification, site initiation, interim monitoring, site management activities and close-out visits (performed on-site or remotely) ensuring regulatory, ICH-GCP and/or GPP and protocol compliance.
• Verifies the process of obtaining informed consent and protects subject confidentiality; assesses factors affecting subject safety and data integrity.
• Assesses site processes, conducts Source Document Review, verifies CRF data accuracy, and drives query resolution.
• Manages IP inventory and ensures proper dispensing per protocol; handles IP labeling/importing as required.
• Prepares for Investigator Meetings and sponsor meetings; supports audit readiness and maintains project documentation.

Skills

Excellent communication

Travel up to 75%

Technical proficiency

Education

Bachelor's degree or RN

Job description

Syneos Health is seeking an Experienced Clinical Research Associate (CRA) regionally aligned across the US. The CRA will monitor sites, ensure regulatory compliance, and collaborate with cross-functional teams to accelerate trial delivery.

This role requires up to 75% travel, strong knowledge of ICH-GCP, data integrity, and excellent communication. On-site or remote monitoring, ISF/TMF coordination, and audit readiness are part of daily responsibilities.