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Job Details

Senior Clinical Research Associate - UK - Can Offer 4 or 5 Days Per Week

Company: Barrington James Clinical
Reference: ACCRAUK100418
Closing Date: 01 Jun 18
Type: Permanent
Salary (£): Competitive

Job Summary:

Exciting oncology division of growing CRO, great culture


Role: Senior Clinical Research Associate (Can consider CRA II)

Location: Home based in the UK

Salary: £40-47,000 + package (Can offer 4 or 5 days per week)


Barrington James are partnering an exciting, financially backed mid-sized CRO as they continue to expand across Europe. Although they have experience in a wide variety of therapy areas, they are well known for the strategic oncology team. You will have the opportunity to work on a number of high profile molecular target cancer therapies, traditional chemotherapy as well as those involving targeted therapies with small molecules, immunotherapy and vaccine, virus and gene therapies.

This is a smaller business unit meaning you have genuine opportunities to grow and take on more responsibility whilst knowing you are working within a stable, global CRO. Also, team member expertise is matched to projects where possible and there is a great team atmosphere.

The role:

  • 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 the CRO to ensure the smooth running of the study
  • To assemble files and ensure documents for the trial master file accurately reflect the progress of the study
  • Other Ad-Hoc CRA duties


To apply:


  • Life Sciences degree
  • Must have strong oncology experience
  • At least 3 years of independent monitoring in a CRO or Pharma
  • ICH GCP and regulatory requirements
  • Experience working within a team environment under time and resource pressures
  • Confident dealing with external and internal clients and providers


For further information on this exciting opportunity, email me via

Apply for this job: Senior Clinical Research Associate - UK - Can Offer 4 or 5 Days Per Week

Contact Information:

Address:  Head Office
Victoria House Consort Way Horley Surrey
Tel:  01293 776644
Fax:  01293 822333
Website:  Visit Our Web Site

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