Senior CRA

Anywhere in UK.
Negotiable and dependant on experience
15 Aug 2019
14 Sep 2019
Part Time
Contract Type
Experience Level
Experienced (non-manager)

This Position is: Permanent and Home Based

We will consider someone 4 days/week.

Covance is looking to recruit an experienced UK based monitor (to work in multiple therapeutic areas) -  at Senior Clinical Research Associate or CRAII level.  This role offers excellent exposure to a range of disease areas.

Team member expertise is matched to projects where possible and we offer a positive and friendly working environment.  Strong team spirit where staff are all pulling together as a cohesive unit with a genuine contribution to global research.

  • The successful applicant will be responsible for coordinating Phase I-IV clinical trials in Europe
  • Perform all types of site visits including, but not limited to, qualification visits, initiation visits, monitoring visits, motivational visits, audit support visits, and termination visits.
  • Assist with document submissions to local authorities
  • To identify potential sites for a proposed study in conjunction with the Project Team, and conduct feasibility assessment of sites as required
  • Ensure that all study related communication including e-mail is tracked, printed and filed as required
  • To track patient recruitment by contacting investigators as specified for the study, and discuss potential study risks and opportunities with the Project Manager and LCRA
  • To liaise with all other appropriate departments within Covance to ensure the smooth running of the study

Additional Information:-

  • Full time permanent position in the UK
  • Applicants must be able to work full time in the UK without restrictions
  • Please send your CV and cover letter to or contact Marc on 0044 1753 216664


  • UK accredited Life Sciences degree or nursing qualification is essential
  • Previous experience of monitoring multiple sites for commercial studies is a must (Please make your experience clear in your application)
  • Significant work experience within the CRA job function
  • Understanding of the principles of ICH GCP and regulatory requirements
  • Good oral and written communication, organizational skills and personal presentation
  • The ability to communicate effectively in English
  • Experience working within a team environment under time and resource pressures
  • Proven experience in clinical trials with knowledge of SOPs, regulatory reporting requirements and accepted practices
  • Confident dealing with external and internal clients and providers

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