Hybrid Clinical Research Associate 2

Posted last week

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About the role

  • Join a dynamic team driving cutting-edge clinical trials! As a CRA, you'll be the key link between sponsors and trial sites—ensuring studies run smoothly, data is accurate, and compliance is top-notch. This role is Perth or Brisbane based. Minimum of 18 months monitoring experience is required. Key Responsibilities include leading site visits (selection, initiation, monitoring, close-out), driving subject recruitment and site engagement to meet study goals, delivering protocol training and maintaining strong site communication, monitoring site performance, escalating quality issues, tracking study progress, maintaining Trial Master File (TMF) and Investigator Site File (ISF), documenting findings and collaborating with cross-functional teams to support project execution, and managing site budgets and invoicing.

Requirements

  • Bachelor’s in science or healthcare (or equivalent experience).
  • 2+ year of on-site monitoring experience.
  • Haematology and Oncology experience.
  • Strong grasp of GCP/ICH and clinical trial protocols.
  • Tech-savvy: MS Office, iPhone/iPad, and remote tools.
  • Excellent communication, organization, and problem-solving skills.
  • Ability to build strong relationships with sites and teams.

Job title

Clinical Research Associate 2

Job type

Experience level

JuniorMid level

Salary

Not specified

Degree requirement

Bachelor's Degree

Location requirements

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