Covance

Senior CRA

Company
Covance
Location
Anywhere in UK.
Salary
Negotiable and dependant on experience
Posted
15 Aug 2019
Closes
14 Sep 2019
Ref
MLJSCRA
Hours
Part Time
Contract Type
Permanent
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 marc.joseph@covance.com or contact Marc on 0044 1753 216664

Requirements:-

  • 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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