Clinical Research Associate: Remote/On-Site Trials

Syneos Health; United States; Hybrid; USD 47,000 - 74,000; Full time

Job summary

Syneos Health is seeking a Clinical Research Associate to support UK multi-sponsor studies. The role involves site qualification, initiation, monitoring, and close‑out visits, on-site or remote, ensuring ICH-GCP compliance and accurate data capture.

You will verify consent, protect patient data, manage ISF/TMF, support recruitment, and help prepare for audits while traveling up to 75%. Bachelor’s degree or RN required; strong communication and computer skills are essential.

Qualifications

• Bachelor’s degree or RN in a related field or equivalent combination of education, training and experience.
• GCP/ICH guidelines knowledge and regulatory requirements.
• Must demonstrate good computer skills and be able to embrace new technologies.
• Excellent communication, presentation and interpersonal skills.
• Ability to travel up to 75% regularly.

Responsibilities

• Performs site qualification, initiation, interim monitoring, site management and close-out visits, on-site or remote, ensuring regulatory, ICH-GCP and/or Good Pharmacoepidemiology Practice (GPP) and protocol compliance.
• Verifies the process of obtaining informed consent and protects subject confidentiality; assesses factors affecting safety and data integrity at investigator sites.
• Conducts Source Document Review of site documents; verifies CRF data accuracy and timeliness; supports query resolution.
• Manages IP inventory and ensures proper dispensing per protocol; handles labeling and release/return as required.
• Maintains ISF vs TMF reconciliation and ensures archiving per local guidelines.
• Documents activities via letters, logs and reports; supports recruitment, retention and data tracking.

Skills

GCP knowledge

Communication

Computer skills

Travel willingness

Education

Bachelor’s degree or RN

Job description

Syneos Health is seeking a Clinical Research Associate to support UK multi-sponsor studies. The role involves site qualification, initiation, monitoring, and close‑out visits, on-site or remote, ensuring ICH-GCP compliance and accurate data capture.

You will verify consent, protect patient data, manage ISF/TMF, support recruitment, and help prepare for audits while traveling up to 75%. Bachelor’s degree or RN required; strong communication and computer skills are essential.