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Manchester   •  £43,000 - 45,000  •  Permanent, Full time

Clinical Research Associate (CRA) 45,000 + Car Allowance Regional Monitoring

A global CRO now has a requirement for a Clinical Research Associate (CRA) to work alongside a team of specialists for a ground-breaking trial. The role will be home based and require travelling to sites regionally.

The successful Clinical Research Associate (CRA) will have experience of working within multiple phases and have experience submitting packages to regulatory authorities and ethical committees.

Essential Skills/Experience: -

Tracking and reporting of essential documents
2 years Independent Monitoring experience
Updating clinical trial systems and databases (CTMS)
Collating, archiving, and distributing study documents (TMF)
Updating study materials (e.g. Patient diaries, instructions)
Organising and supporting meetings, including investigator meetings
Life Sciences / Healthcare Degree
Strong organisational and communication skills
Ability to work in a cross functional team

Desired Skills/Experience: -

Updating investigator lists for site evaluation and start up activities
Preparing packages for submissions to Regulatory authorities and Ethical committees
Working closely with finance teams for tracking and reporting of budget negotiations, contract development and management of investigator and site payments

If you feel as though you, or someone you know, would be suitable for the position of a Clinical Research Associate (CRA) feel free to get in touch on 01189 594990. Alternatively, you can email me directly at fawad.siddiqui@cpl.com

  • Agency: Cpl Life Sciences
  • Contact: Fawad Siddiqui
  • Reference: JO-2101-461659
  • Posted: 2nd June 2021
  • Expires: 30th June 2021

Cpl Life Sciences

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