Covance Clin Res Assoc II in Brussels, Belgium

Job Overview

Covance is looking for a seasoned CRA to join our team and the one of one of our main client in Belgium!

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)

  • In lieu of the above requirement, candidates with three (3) or more years of relevant clinical research experience in pharmaceutical or CRO industries may be considered

  • Thorough knowledge of ICH Guidelines and GCP including a basic understanding of regulatory requirements

  • Thorough knowledge of monitoring procedures

  • Basic understanding of the clinical trial process

Experience

Required:

  • Minimum of two (2) years of clinical research monitoring experience (including pre-study, initiation, routine monitoring and closeout visits)

  • Ability to monitor study sites independently according to protocol monitoring guidelines, SOPs, GCP and ICH Guidelines

  • Have a full understanding of the Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs

  • Good planning, organization and problem solving abilities

  • Ability to work with minimal supervision

  • Good communication and interpersonal skills

  • Good analytical and negotiation skills

  • Computer competency

  • Fluent in local office language and in English, both written and verbal

  • Works efficiently and effectively in a matrix environment

Preferred:

  • One (1) or more additional years of experience in a related field (i.e. medical, clinical, pharmaceutical, laboratory, research, data analysis, data management or technical writing) is preferred

Job Number 2018-24300

Job Category Clinical Research Associate

Position Type Full-Time

Covance is committed to diversity in the workplace and is an equal opportunity employer (Minority/Female/Individual with Disability/Veteran/Sexual Orientation/Gender Identity). Your confidentiality and privacy are important to us.