• Senior Clinical Research Associate II

    Job Location(s) AU-Sydney | AU-Melbourne
    Job Number
    Job Category
    Clinical Research Associates
    Position Type
  • Job Overview

    Are you an exceptional Senior Clinical Research Associate (SCRA) based in Australia that has independent trial site monitoring experience and would like to experience working at a client site while remaining an employee of Covance?


    Our Flexible Solutions Clinical Research Associates enjoy the best of both worlds, you are a permanent employee of a growing Clinical Research Organisation; Covance while developing your knowledge in a global pharmaceutical company. You will join an exceptional team with talented managers who will support you and help grow your career across the Covance family. 


    Your responsibilities include:

    • Lead all aspects of study site monitoring according to Covance/Chiltern SOP, GCP, and ICH guidelines
    • Partner with investigators and study coordinators on pre-study qualification and site initiation visits
    • Conduct routine study site monitoring visits
    • Close-out clinical sites, and ensure study files are up to date to maintain the success of the study.

    Covance Australia is committed to providing Clinical Research Associates; flexibility to work from home, the freedom to grow your career across all phases and areas of clinical trial operations, and provides you with cutting edge technology and processes that help to manage your time and workload.


    Want to learn more? Hear from some of the team through our Covance Australia CRA microsite.


    About Covance:


    Covance is one of the world’s largest and most comprehensive drug development services companies, with more than 13,000 employees in 60 countries. We began operations Asia Pacific in 1988 and today have more than 1000 employees in 14 countries across the region.Covance has helped pharmaceutical and biotech companies develop one-third of all prescription medicines in the market today.


    Why Covance?


    At Covance, you will join like-minded collaborative professionals who, together, build our reputation as one of the world's largest and most respected contract research organizations. In choosing Covance, you will be part of a dedicated team that makes a difference in helping to deliver life-saving and life-enhancing medicines to people around the world.


    Discover your potential in a company that truly invests in you. Talk to us to learn more and explore your career. Apply online today.


    • Degree Qualified 


    • Ability to monitor study sites independently according to protocol monitoring guidelines, SOPs, GCP and ICH Guidelines
    • Excellent understanding of Serious Adverse Event (SAE) reporting
    • Typically 3+ years of clinical research monitoring experience (including pre-study, initiation, routine monitoring and closeout visits).
    • Knowledge of the Australian site and regulatory environment is beneficial
    • Previous experience monitoring Oncology clinical trials is preferred


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