Remote Clinical Research Associate - Drive Global Trials

Syneos Health, Inc.; Wyoming (OH); Hybrid; USD 70,000 - 110,000; Full time

Job summary

Syneos Health in the United States is seeking a Clinical Research Associate for Full-Service operations. This role emphasizes remote site monitoring, regulatory compliance, and collaboration with cross-functional teams to accelerate trial delivery.

The CRA will perform site qualification, initiation, monitoring, and close-out visits (on-site or remote); verify informed consent; manage data quality; and support IP handling. Excellent communication and travel up to 75% are required.

Qualifications

• Bachelor’s degree or RN in related field or equivalent.
• Knowledge of Good Clinical Practice/ICH Guidelines.
• Strong computer skills and ability to adopt new technologies.
• Excellent communication, presentation and interpersonal skills.
• Ability to travel up to 75%.

Responsibilities

• Performs site qualification, initiation, interim monitoring, site management activities and close-out visits (on-site or remotely) ensuring regulatory, ICH-GCP and/or GPP and protocol compliance.
• Verifies informed consent processes and protects confidentiality; assesses safety and data integrity at investigator sites.
• Reviews ISF/TMF, ensures data accuracy, performs query resolution, and supports monitoring processes.
• Manages IP inventory, labeling, storage, and release according to protocol; ensures compliance with regulations.
• Documents activities, supports recruitment and data tracking, and maintains project documentation.

Skills

GCP/ICH knowledge

Strong communication

Computer skills

Travel readiness

Education

Bachelor’s degree or RN

Job description

Syneos Health in the United States is seeking a Clinical Research Associate for Full-Service operations. This role emphasizes remote site monitoring, regulatory compliance, and collaboration with cross-functional teams to accelerate trial delivery.

The CRA will perform site qualification, initiation, monitoring, and close-out visits (on-site or remote); verify informed consent; manage data quality; and support IP handling. Excellent communication and travel up to 75% are required.