Remote-Ready Clinical Research Associate II

Syneos Health; Kansas; On-site; USD 70,000 - 100,000; Full time

Job summary

Syneos Health is seeking an Experienced Clinical Research Associate II to support site monitoring across multiple studies. You will conduct qualification, initiation, monitoring, and close-out visits, ensuring GCP/ICH compliance and subject protection.

The role requires strong communication, data quality focus, and the ability to travel up to 75% while collaborating with sponsors and sites to meet study timelines.

Qualifications

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

Responsibilities

• Conduct site qualification, initiation, interim monitoring, and close-out visits per protocol (on-site or remote).
• Verify informed consent and protect subject confidentiality; assess patient safety and data integrity.
• Perform source data review and CRF data reconciliation; drive timely query resolution.
• May handle IP inventory, labeling, and reconciliation according to protocol.
• Maintain ISF and TMF accuracy; ensure archiving per local guidelines.

Skills

Communication skills

Interpersonal skills

Presentation skills

Computer skills

Travel readiness

Education

Bachelor’s degree or RN in a related field

Tools

MS Office

Job description

Syneos Health is seeking an Experienced Clinical Research Associate II to support site monitoring across multiple studies. You will conduct qualification, initiation, monitoring, and close-out visits, ensuring GCP/ICH compliance and subject protection.

The role requires strong communication, data quality focus, and the ability to travel up to 75% while collaborating with sponsors and sites to meet study timelines.