Clinical Research Associate I/II – Remote/Onsite

Syneos Health Clinical; Australia; Híbrido; AUD 70.000 - 110.000; Jornada completa

Descripción de la vacante

Syneos Health Clinical is seeking a Sr. CRA I to support site qualification, initiation, monitoring, and close-out visits. You will ensure regulatory, ICH-GCP and local requirements are met while protecting patient safety and data integrity.

The role involves on-site and remote work with substantial travel (up to 75%) to sites, sponsors, and meetings. Strong communication and organizational skills are essential for success in a fast-paced, global environment.

Formación

• 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.
• Excellent communication, presentation and interpersonal skills.
• Basic level of critical thinking skills expected.
• Ability to manage required travel up to 75% on a regular basis.

Responsabilidades

• Performs site qualification, initiation, interim monitoring, site management and close-out visits (on-site or remote) ensuring regulatory, ICH-GCP and/or GPP compliance.
• Verifies informed consent has been adequately performed and documented for each subject/patient as required.
• Conducts Source Document Review and verifies CRF data accuracy and completeness.
• Applies query resolution techniques remotely and on site to drive timely closure.
• Maintains ISF/TMF and supports audit readiness; assists with site training and mentoring junior staff.
• Supports subject recruitment, retention and awareness strategies; tracks observations and action items.

Conocimientos

Bachelor's degree or RN

GCP/ICH knowledge

Strong communication

Presentation skills

Interpersonal skills

Critical thinking

Travel ability

Educación

Bachelor's degree or RN in life sciences

Herramientas

Microsoft Office

Computer skills

Descripción del empleo

Syneos Health Clinical is seeking a Sr. CRA I to support site qualification, initiation, monitoring, and close-out visits. You will ensure regulatory, ICH-GCP and local requirements are met while protecting patient safety and data integrity.

The role involves on-site and remote work with substantial travel (up to 75%) to sites, sponsors, and meetings. Strong communication and organizational skills are essential for success in a fast-paced, global environment.