Clinical Trial Nurse at Vial Health Technology
Sydney, New South Wales, Australia -
Full Time


Start Date

Immediate

Expiry Date

28 Nov, 25

Salary

0.0

Posted On

29 Aug, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Good communication skills

Industry

Pharmaceuticals

Description

WHO WE ARE

Battery Bio is the Australian arm of Vial, a cutting-edge clinical research organization dedicated to advancing innovative therapeutics through efficient clinical trials. Based in Australia, Battery Bio leverages local expertise and infrastructure to conduct high-quality clinical trials for Vial’s extensive drug portfolio.
Our mission is to bring transformative medicines to patients by executing world-class clinical research in Australia. We combine Vial’s innovative approach to clinical trials with Australia’s robust regulatory framework and experienced clinical research community.
Battery Bio operates as a key strategic partner in Vial’s global clinical development programs, providing access to Australia’s diverse patient populations and streamlined regulatory pathways. We are committed to maintaining the highest standards of clinical research while accelerating the development of life-changing therapies.

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Responsibilities

WHAT YOU’LL DO

Reporting into Battery Bio’s clinical operations team, we are seeking a Clinical Trial Nurse to support our Phase 1 Clinical trials in Australia. This role is pivotal in executing high-quality clinical research and will play a critical role in bringing new medicines to patients. The ideal candidate will work collaboratively with our clinical team and be comfortable managing multiple responsibilities in a fast-paced environment.

KEY RESPONSIBILITIES

  • Support the Principal Investigator and Sub-Investigators in executing all aspects of the clinical trial protocol
  • Perform clinical procedures including drug dosing, lab draws, vital signs monitoring, and other protocol-required assessments
  • Ensure smooth patient flow through study visits
  • Maintain accurate and timely source documentation and patient records in compliance with GCP standards
  • Collaborate with the clinical research team, including coordinators and site staff, to ensure trial success
  • Monitor patient safety and promptly report any adverse events or protocol deviations
  • Contribute to regulatory compliance activities and support audit preparation
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