Thrive in a Collaborative Environment and Advance your Career
Are you an organized person who can work independently and take ownership of your career? Would you like to gain on-the-job skills while helping advance life-changing medicines?
If you are looking to enter a nurturing environment that provides a clear path to advancement, consider furthering your career as a Covance Clinical Research Associate (CRA). In this role, you will:
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) • 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
Minimum six (6) months of clinical research experience including demonstrated competency in site monitoring (including pre-study, initiation, routine monitoring and closeout visits) • In lieu of the above requirements, candidates with two (2) years of site management and/or study coordinator experience may be considered • Ability to monitor study sites according to protocol monitoring guidelines, SOPs, ICH Guidelines and GCP • Ability to work within a project team • Good planning, organization and problem solving abilities • Good communication skills, oral and written • Good computer skills • Works efficiently and effectively in a matrix environment • Fluent in local office language and in English, both written and verbal