Covance Sr Clin Res Assoc in Paris, France

Job Overview

Covance is recruiting an experienced CRA to be dedicated to a very innovative biotech. This role is office-based in the paris area, North of France or Nantes. This is a great opportunity to join our organisation and to be part of a very dynamic and motivationf work environment.

This is time to join our EMEA FSPx Team!

Education / Qualifications

  • External Candidates

  • University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure),

AND

  • a minimum of 4 years of Clinical Monitoring experience

  • In lieu of the above education requirement, external candidates with a minimum of 6 years recent clinical monitoring experience will be considered

  • Internal Candidates

  • Internal candidates with a minimum of 4 years of clinical monitoring experience.

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

  • Thorough understanding of the drug development process

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

Experience

  • External Candidates

  • University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure),

AND

  • a minimum of 4 years of Clinical Monitoring experience

  • In lieu of the above education requirement, external candidates with a minimum of 6 years recent clinical monitoring experience will be considered.

  • Internal Candidates

  • Internal candidates with a minimum of 4 years of clinical monitoring experience.

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

  • Advanced site monitoring skills

  • Advanced study site management skills

  • Advanced registry administration skills

  • Ability to work with minimal supervision

  • Good planning and organization skills

  • Good computer skills with good working knowledge of a range of computer packages

  • Advanced verbal and written communication skills

  • Ability to train and supervise junior staff

  • Ability to resolve project-related problems and prioritizes workload for self and team

  • Ability to work within a project team

  • Works efficiently and effectively in a matrix environment

Job Number 2018-24303

Job Category Clinical Research Associate

Position Type Full-Time

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