Senior / Clinical Research Associate

IQVIA ANZ | Global CRO | Career Growth + Variety

Perth WA

Ready to take your CRA career somewhere it can grow?

At IQVIA, we’re not just running studies—we’re shaping the future of healthcare. We’re looking for a Clinical Research Associates (CRA) at all levels who want more than just another monitoring job: someone who wants exposure, development, and meaningful impact.

Why this role stands out

As a CRA at IQVIA, you’ll go beyond compliance checking—you’ll be a trusted partner to sites, helping them succeed and deliver high-quality outcomes across diverse clinical programs.

You’ll gain:

• Exposure to a broad range of therapeutic areas (not stuck in just one)

• Global CRO backing with local flexibility

• Structured training + mentoring to accelerate your career

• Opportunities to work closely with leading sponsors and research sites

What you’ll be doing

• Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International

• Conference on Harmonization (ICH) guidelines

• Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.

• Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.

• Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.

• Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution.

• May support start-up phase.

• Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.

• Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.

• Collaborate and liaise with study team members for project execution support as appropriate.

Qualifications:

• Bachelor’s degree in a scientific or healthcare discipline preferred.

• At least 4 years of on-site monitoring experience (across ANZ)

• Prior Oncology trial management exposure ideal.

• Strong knowledge of GCP and ICH guidelines.

• Proficiency in Microsoft Office and relevant technology.

• Excellent written and verbal skills.

• Strong organizational and problem-solving abilities.

• Effective in managing time and finances.

• Ability to build and maintain strong relationships with coworkers, managers, and clients.

• Full time permanent working rights in Australia
  

Recruitment Process

To help us get to know you better, shortlisted candidates will complete a short video screening step as part of the process.

IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world.

Learn more at  https://jobs.iqvia.com