Senior Clinical Research Associate

  • Melbourne, Victoria
  • Permanent

Our client seeks an experienced Senior Clinical Research Associate (CRA) to oversee and monitor clinical trials across diverse therapeutic areas.

Founded in the late 1990s, this award-winning firm has established itself as a global leader, operating in over 30 countries.

They offer a supportive work environment with flexible onsite requirements and manageable workloads.

Ideal for a seasoned Clinical Research Associate with a minimum of 2 years' CRO/Pharma monitoring experience.

Key Responsibilities:

  • Initiate, monitor, and conclude site visits globally, ensuring adherence to protocols and regulatory standards.
  • Identify suitable global clinical trial sites through site selection and qualification activities.
  • Collaborate with cross-functional teams, including investigators and project managers, to ensure seamless trial execution.
  • Verify clinical data accuracy and compliance with study protocols and regulatory requirements.
  • Maintain essential study documentation, including regulatory submissions and monitoring reports.
  • Address and escalate issues related to patient safety, data integrity, or study conduct.
  • Contribute to protocol development, case report forms (CRFs), and other study-related documents.
  • Train and mentor junior CRAs, offering support as required.


  • Bachelor's degree in a scientific or healthcare discipline; advanced degree preferred.
  • Minimum 2 years' experience as a Clinical Research Associate, ideally in global clinical trials.
  • Proficiency in ICH-GCP guidelines, local and international regulatory requirements, and industry standards.

Position Details:

Title: Senior CRA

Salary: $120,000 - $155,000 plus superannuation

Location: Melbourne, South Australia, Western Australia

To apply for this opportunity, please submit your updated resume or contact Keeley Munday at 02 8310 5854.

Related Keywords: Clinical Research Associate, CRA, Global Clinical Research Organisation, global clinical trials, therapeutic areas, ICH-GCP guidelines, site selection, data integrity, patient safety, regulatory compliance, cross-functional teams, site visits, biotech-sponsored projects, mentoring, junior CRAs, EDC systems, global travel, professional growth, innovation, impactful research, healthcare

Keeley Munday Principal Candidate Consultant

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