Research Associate Sr. in cancer research at Duke, developing T cell therapies and collaborating across teams. Ensuring research throughout preclinical models to clinical trials.
About the role
- CRA role overseeing clinical trial execution, ensuring compliance and communication between sponsors and sites. Focused on site performance and data accuracy while based in Brisbane or Perth.
Responsibilities
- 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
Job type
Experience level
Salary
Not specified
Degree requirement
Tech skills
Location requirements
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