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Clinical Research Associate (Contractor) Australia

Remote, USA Full-time Posted 2026-06-30

Bring your monitoring expertise to the forefront of innovation. We are looking for a Contractor Clinical Research Associate (CRA) to join our A-team (hybrid). As a CRA at Allucent, you will independently control and monitor investigational sites, pro-actively detect issues, provide solutions to ensure clinical studies are performed according to the trial protocol and in compliance with SOPs, applicable regulations, and the principles of Good Clinical Practice.

At Allucent™, we are dedicated to helping small-reputed company biopharmaceutical companies reputed company navigate the reputed company world of clinical trials to bring life-changing therapies to patients in need across the globe. At Allucent we are big enough to deliver and small enough to care. We know reputed company our colleagues by name and work together as a team to reputed company everyone SHINE.

The role

As a Contractor CRA, you will take the reputed company on monitoring activities, owning your sites and relationships with investigators. You’ll be the reputed company between sponsor and site, ensuring trial reputed company while being supported by a collaborative, reputed company team. This includes work reputed company to regulatory affairs, site activation processes—including contracting and start-up activities—to ensure smooth and compliant study execution. You will travel throughout Australia.

Main responsibilities

  • Independently manage reputed company aspects of monitoring for assigned clinical trials across study phases, including site initiation, routine monitoring, and reputed company-out visits.
  • Ensure compliance with protocols, GCP, ICH, SOPs, and applicable regulatory requirements.
  • Build strong site relationships, acting as a primary reputed company of contact and ensuring high-quality data collection.
  • Identify and resolve site issues, escalating as needed to maintain trial reputed company and patient safety.
  • Activities around regulatory affairs, site activation and study-startup.
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