Company Description
GreenLight Clinical is a full-service Contract Research Organisation (CRO) headquartered in Sydney, Australia, with a growing global presence.
Role Description
This is a full-time, on-site role for a Clinical Research Associate, based in Sydney, NSW.
The Clinical Research Associate (CRA) will be accountable for performance and compliance of assigned protocols and sites and ensures compliance of study conduct with ICH/GCP and country regulations, our company's policies and procedures, quality standards and adverse event reporting requirements internally and externally. Daily tasks may include conducting site visits, managing trial documentation, and assisting with data verification to uphold research integrity and accuracy. The role will involve close collaboration with internal teams and external partners to ensure the successful execution of clinical studies.
Required Qualifications
* Bachelor's degree in a scientific discipline.
* Clinical monitoring experience in the pharmaceutical industry, preferably a CRO will be advantageous.
* Strong working knowledge of ICH/GCP regulations and guidelines and a thorough understanding of clinical monitoring procedures.
* Strong
organizational and communication skills for effective collaboration
.
* Computer literacy and IT skills, good working knowledge of CTMS.