Clinical Research Quality Assurance Lead

1 week ago

Sydney, New South Wales, Australia On Q Recruitment Full time

Are you passionate about delivering the highest standards of quality in clinical trials?

  • Contribute to groundbreaking cancer research that improves outcomes and quality of life for the patient.
  • Part-Time, open to 3 to 4 days work per week.
  • Flexible working arrangement - can be based in Sydney or Melbourne.

Join a Leading Gynaecological Cancer Research Organization, committed and working tirelessly to develop groundbreaking treatments and improve the quality of life for patients.

They are a growing cancer trial collaborative group that accelerated their team growth over the last 4 years and has been working closely with over 1400 members across the life science industries with a vision to make a difference in advancing research that has the potential to transform the lives of patients with gynaecological and ovarian cancer.

We are seeking a dedicated Clinical Research Quality Assurance Lead to join this peak national gynaecological cancer research organization where you will play an important role in enhancing quality systems.

This is a newly created role where you will establish and implement a robust clinical quality assurance framework, strengthening their existing standard operating procedures, policies, and QMS system. You will be working alongside the leadership team, showcasing your ability to provide strategic input and corrective actions on quality-related matters, and your ability to recommend with confidence on a series of initiatives in oncology research.

Guided by your expertise in GCP, you will be a subject matter expert in finessing and improving quality as the trial groups grow, ensuring auditing and quality compliance with relevant regulations while driving continuous improvement such as overseeing site vendor selection and performance and delivering and monitoring GCP training compliance.

To be successful in this role:

  • Tertiary degree or equivalent work experience in a discipline relevant to clinical trials; Oncology clinical trials experience is preferred.
  • An in-depth understanding of health research and the clinical trials operations processes.
  • Comprehensive knowledge of clinical trial quality management, GCP, compliance audits, and other regulatory requirements.
  • High level of organisation, problem-solving, and analytical skills.
  • Demonstrated competency in strategic thinking; capable of influencing senior leadership and working collaboratively with changing stakeholders.

What else is on offer:

  • Part-Time position, looking at between 3 to 4 days of work per week.
  • Flexible working arrangement - can be based in Sydney or Melbourne.
  • Offering a hybrid working arrangement of 1 day per fortnight in the office.
  • Competitive salary packaging with NFP benefits - ability to salary sacrifice up to $16k per year. This means you can expense a portion of your salary on expenses to increase take-home pay.
  • Work alongside a multidisciplinary team of dedicated professionals in a supportive and inclusive environment.
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