Job Overview :
Are you an exceptional Clinical Research Associate (CRA) based in Taiwan that has independent trial site monitoring experience and would like to experience working as a CRA at a pharmaceutical company while remaining a permanent employee of Covance?
Our Flexible Solutions Clinical Research Associates are based at our pharmaceutical client sites and manage all aspects of study site monitoring according to Client SOP, GCP, and ICH guidelines, including pre-study qualification and initiation visits, routine monitoring, close-out of clinical sites, and maintenance of study files.
query generation and resolution against established data review guidelines on Covance or client data management systems as assigned by management May support in organization of meetings and other tasks as instructed by supervisor
Covance Taiwan is committed to providing Clinical Research Associates; the flexibility to work from home, the freedom to grow careers across all phases and areas of clinical trial operations as well as providing technology and processes that help to manage time and workload.
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.
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.
Education / Qualifications :
University / college degree (life science preferred), or certification in a related allied health profession from an appropriately accredited institution (e.
g., nursing certification, medical or laboratory technology) Experience : In lieu of the above requirement, candidates with two (2) or more years of relevant clinical research experience in pharmaceutical or CRO industries may be considered Basic understanding of ICH Guidelines and GCP including a basic understanding of regulatory requirements Basic understanding of the clinical trial process