Join a Purpose-Driven Organisation Advancing Early-Phase Clinical Research

Are you passionate about quality, detail-oriented, and ready to take the next step in your QA career? This is an exciting opportunity to join a pioneering clinical research organisation at the forefront of early-phase trials. With a dedicated focus on patient safety, innovation, and regulatory excellence, this team is making a meaningful impact on the future of medicine.

As a Quality Associate, you’ll play a vital role in supporting clinical study compliance, ensuring adherence to global standards, and contributing to process improvement across the board. This is a dynamic role ideal for someone who thrives in a collaborative environment, enjoys problem-solving, and is eager to grow their career in the clinical research space.

Responsibilities:

Support the maintenance and improvement of the Quality Management System (QMS).

Assist in the development and review of SOPs and quality documentation.

Manage electronic quality systems including Dot Compliance and SiteDocs.

Support audits, inspections, and CAPA tracking.

Assist with equipment calibration, validation, and computer system validation (CSV).

Monitor training, deviations, and quality events via eQMS reporting.

Support internal audits and vendor qualification activities.

Contribute to the delivery of quality training for clinical teams.

Skills:

Bachelor’s or advanced degree in life sciences, healthcare, or a related field.

Experience in a quality-focused role — clinical research or GCP experience is highly regarded but not essential.

Strong attention to detail and a commitment to quality and compliance.

Comfortable working with systems and databases (training can be provided).

Proactive and curious, with a willingness to ask questions, learn, and grow within the role.

Able to work both independently and collaboratively in a fast-paced, evolving environment.

Apply directly now, or send your updated CV to Ben Byrne at [email protected] OR 0421776703.