Job Description
The Clinical Research Associate 2 plays a vital role in the Clinical Operations group, overseeing site management, monitoring tasks, and operational support for clinical trials.
Responsibilities include coordinating investigator and site selection, completing monitoring activities, preparing site evaluation reports, negotiating site budgets, and ensuring timely site payments.
Required Skills & Qualifications
* Tertiary qualifications in a related science or healthcare discipline
* Previous experience in clinical trials within an academic, CRO, or pharmaceutical environment with 2-5 years of monitoring and site management experience
* Demonstrate practical knowledge of ICH-GCP guidelines and global/local ethical and regulatory research requirements
* Display competence in technical areas such as ethical/participant safety considerations, site start-up management, site conduct management, risk management, quality management, supply management, scientific concepts, and issue escalation management
* Business skill areas including negotiation/conflict resolution, critical thinking/problem-solving, decision making/strategic thinking, solid interpersonal communication/presentation skills, and flexibility to work in a multi-disciplinary team
Benefits
* Competitive compensation package
* Flexible/hybrid working arrangements
* Career growth opportunities
* Employee wellbeing initiatives
* Global opportunities for professional development
Why Join Us?
At our core, we're committed to transforming clinical research by prioritizing people – patients and employees alike. Join us to contribute to trials that genuinely improve lives, fostering collaboration and innovation while connecting with local communities.