Site Monitoring Pro for Clinical Trials

Syneos Health, Inc.; Adelaide; On-site; AUD 70,000 - 95,000; Full time

Job summary

Syneos Health, Inc. in Australia is seeking a Clinical Research Associate I for Real World Late Phase studies. The role supports site qualification, initiation, and monitoring visits, ensuring regulatory compliance and data integrity.

Responsibilities include source data verification, IP handling, and ISF/TMF reconciliation, with collaboration across sponsor teams. Travel up to 75% is required, with on-site or remote activities as applicable.

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 (on-site or remote) ensuring regulatory, ICH-GCP and/or GPP compliance.
• Verifies informed consent and protects subject confidentiality; assesses safety and data integrity at sites.
• Documents activities and supports audit readiness; conducts Source Document Review and data verification.
• Manages IP inventory, labeling, storage, and route to ensure protocol compliance.
• Supports recruitment, tracking observations, and communication with sponsor teams.

Skills

Communication skills

Interpersonal skills

Presentation skills

Computer skills

Travel readiness

Education

Bachelor’s degree or RN in a related field

Job description

Syneos Health, Inc. in Australia is seeking a Clinical Research Associate I for Real World Late Phase studies. The role supports site qualification, initiation, and monitoring visits, ensuring regulatory compliance and data integrity.

Responsibilities include source data verification, IP handling, and ISF/TMF reconciliation, with collaboration across sponsor teams. Travel up to 75% is required, with on-site or remote activities as applicable.