Clinical Research Associate: Site Management (Remote/Travel)

Syneos Health, Inc.; United States; Remote; USD 65,000 - 90,000; Full time

Job summary

Syneos Health is seeking a Clinical Research Associate I to perform site qualification, initiation, monitoring, and close-out visits, ensuring regulatory and GCP compliance. You will verify informed consent, monitor data quality, and manage site communications.

Role requires up to 75% travel, strong computer skills, and excellent communication. A Bachelor’s degree or RN is required. This position is based in the United States with on-site responsibilities.

Qualifications

• Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements.
• Bachelor’s degree or RN in related field.
• Excellent communication, presentation and interpersonal skills.
• Must demonstrate good computer skills and be able to embrace new technologies.
• 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 (on-site or remotely) ensuring regulatory, ICH-GCP and/or Good Pharmacoepidemiological Practices (GPP) and protocol compliance.
• Verifies informed consent processes and maintains patient confidentiality and data integrity.
• Conducts CMP/SMP activities, source data review, and data verification in CRFs.
• Manages IP inventory, reconciliation, labeling, and shipment according to protocol.
• Reviews Investigator Site Files for accuracy and archiving requirements.
• Documents activities and supports recruitment, retention and tracking of observations and actions.
• Coordinates with project team to ensure timelines and deliverables are met.
• Acts as liaison with site personnel and supports training and audit readiness.

Skills

GCP/ICH knowledge

Excellent communication

Strong computer skills

Travel up to 75%

Team collaboration

Education

Bachelor’s degree or RN in related field

Tools

MS Office

Job description

Syneos Health is seeking a Clinical Research Associate I to perform site qualification, initiation, monitoring, and close-out visits, ensuring regulatory and GCP compliance. You will verify informed consent, monitor data quality, and manage site communications.

Role requires up to 75% travel, strong computer skills, and excellent communication. A Bachelor’s degree or RN is required. This position is based in the United States with on-site responsibilities.