CRA I/II — Site Management & Data Integrity

Parexel International; Sydney; On-site; AUD 90,000 - 120,000; Full time

Job summary

Parexel International is seeking a Clinical Research Associate I/II for the Core Team, based in Sydney or Melbourne. The role involves on-site monitoring, site liaison, and ensuring protocol adherence across trial activities.

You will manage site relationships, coordinate visits, ensure training, and support data integrity, with travel as required. Strong communication and problem-solving are essential, along with experience in clinical trials and ICH-GCP.

Qualifications

• Site management experience in clinical research.
• Degree in biological science or health-related discipline.
• Strong communication and problem-solving skills.

Responsibilities

• Act as Parexel's contact with assigned sites through lifecycle.
• Monitor site activities to ensure protocol compliance.
• Facilitate site access to study systems and training.
• Coordinate site visits and remote contacts.
• Review and approve site documentation and TMF submissions.
• Support data quality and query resolution at sites.
• Prepare reports and participate in audits or inspections.

Skills

Site management

Clinical monitoring

Data quality

Problem solving

Independent work

Travel flexibility

Education

Biological science degree

Tools

CTMS

EDMS

MS Office

Job description

Parexel International is seeking a Clinical Research Associate I/II for the Core Team, based in Sydney or Melbourne. The role involves on-site monitoring, site liaison, and ensuring protocol adherence across trial activities.

You will manage site relationships, coordinate visits, ensure training, and support data integrity, with travel as required. Strong communication and problem-solving are essential, along with experience in clinical trials and ICH-GCP.