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Tech Stack
Tools & technologiesGoogle Cloud Platform
About the role
Key responsibilities & impact- Maintenance (from initiation through close out): Act as Parexel’s direct contact with assigned sites
- Assess and ensure overall integrity of study implementation and adherence to study protocol at clinical sites
- Build relationships with investigators and site staff
- Facilitate and support site with access to relevant study systems
- Evaluate if on-site staff assignment is still accurate
- Address and resolve issues at sites
- Collect, review, and approve updated/amended site documentation
- Monitor and maintain compliance with ICH-GCP and applicable international and local regulations
- Ensure timely and accurate completion of project goals
- Maintain a positive, results-orientated work environment.
Requirements
What you’ll need- CRA experience from AUS or NZ is required (at least 1 year of independent monitoring)
- Sound problem solving skills
- Able to take initiative and work independently
- Advance presentation skills
- Client focused approach to work
- Ability to interact professionally within a client organization
- Flexible attitude with respect to work assignments and new learning
- Ability to prioritize multiple tasks and achieve project timelines
- Strong computer skills including but not limited to the knowledge of a Clinical Trial Management System (CTMS), Electronic Document Management System (EDMS), and MS-Office products such as Excel and Word
- Developing ability to work across cultures.
Benefits
Comp & perks- Open to consider experienced CRAs based in Melbourne or Sydney.
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
CRA experienceindependent monitoringproblem solvingpresentation skillsproject managementcompliance monitoring
Soft Skills
initiativeindependenceclient focusprofessional interactionflexibilityprioritizationcross-cultural communication
