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Clinical Research Associate - Leading Global CRO

Your new company
You will be working for an established, full-service CRO based in Manchester.  You will be working in a company with a strong focus on developing their employees.  This is an exciting time to join as the company is gaining strong results and will need a CRA to hit the ground running.

Your new role
You will be working as an office based CRA, monitoring on studies predominantly in Phases II and III.

  • Ensure investigator compliance with protocol, study procedures, regulatory requirements and timelines
  • Interact directly with clinical sites, including clinical investigators and other health care professionals involved in the clinical study and maintain a positive rapport with each site
  • Collection of essential documents from site applicable for submission and trial master file
  • Oversight and support of sites with recruitment and retention strategies and perform motivational visits if needed
  • Site management and remote monitoring in order to support investigational sites

What you'll need to succeed
You will need at least 6 months of monitoring experience, ideally within Phases II and III.  You will need to have a proactive attitude to facing challenges.

What you'll get in return
You will be working for a global CRO with an excellent reputation within the market.  You will gain excellent experience on top of strong scope for career development.

What you need to do now
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.
If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career.


Job Type:
Life Sciences
Apply Now

Talk to a Consultant

Talk to Alexander Clark, the specialist consultant managing this position, located in London City

107 Cheapside, London, EC2V 6DN

Telephone: 02034650079

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