Clinical Research Associate I – II

This is a fully remote position, open to applicants in Australia.

📋 Description

• Oversee maintenance activities (from initiation to close out): Serve as Parexel’s primary liaison with designated sites.

• Evaluate and ensure the overall integrity of study execution and compliance with the study protocol at clinical locations.

• Cultivate relationships with investigators and site personnel.

• Facilitate and assist sites in accessing pertinent study systems.

• Assess whether the on-site staff assignments remain accurate.

• Identify and resolve issues at the sites.

• Gather, review, and authorize updated or amended site documentation.

• Monitor and ensure compliance with ICH-GCP as well as relevant international and local regulations.

• Guarantee timely and precise completion of project objectives.

• Foster a positive, results-driven work atmosphere.

⛳️ Requirements

• A minimum of 1 year of independent monitoring CRA experience from AUS or NZ is essential.

• Strong problem-solving abilities.

• Capable of taking initiative and working autonomously.

• Advanced presentation skills.

• A client-focused approach to work.

• Proficient in interacting professionally within a client organization.

• Flexible attitude regarding work assignments and new learning opportunities.

• Ability to prioritize numerous tasks and meet project deadlines.

• Strong computer proficiency, including knowledge of a Clinical Trial Management System (CTMS), Electronic Document Management System (EDMS), and MS-Office applications like Excel and Word.

• Developing ability to work within diverse cultural environments.

🏝️ Benefits

• Open to considering experienced CRAs located in Melbourne or Sydney.