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Job Details

Clinical Research Associate

Company: Chiltern
Location: Anywhere in UK
Reference: MLJ NOV 123
Closing Date: 02 Jan 17
Type: Permanent
Salary (£): 30,000 - 40,000
Benefits: competitive salary, car/car allowance, pension, LI, 25 days leave

Job Summary:

We have a number of current opportunities with a top ten pharmaceutical company. These are all home based full time CRA positions. Chiltern have enjoyed a long and partnered approach with this company and both organisations are focused on the wellbeing and career development of this large team.

Requirements:

You would be permanently employed by Chiltern on PAYE salary and benefits, and seconded to our client. We offer a competitive salary, car/car allowance, pension, LI, 25 days leave (increasing to 30) and other pastoral/quality of life benefits including contributions towards health club membership.

We are looking for dynamic CRAs – individuals who enjoy the thrill of building relationships with sites, are interested in career development and appreciate the benefits of being “employed” for example, career development opportunities hand in hand with Chiltern and our client.

You will receive full support in terms of line management/pastoral care, full administrative support, and access to excellent training in both soft skills and technical advancement courses.
Working within a large cross section of therapy areas, this is a rolling and renewable contract starting as a 12 months secondment. Opportunities currently exist in the following regions; Southeast, Southwest, Midlands, the North of England and throughout Ireland.

You would typically be monitoring around 3 days/week, sometimes more sometimes less. Sites are all very regional so travel distance is minimal but there will be multiple protocols.

IMPORTANTLY - We are looking for CRAs who have at least 12 months independent monitoring experience at hospital sites either in the UK or Ireland. You may have been doing this within an academic setting and/or within an NHS trust - that is fine, as long as you have the independent monitoring skills to include site selection, initiation, monitoring and close out.

DUTIES

  • Contribute to the nomination of new sites for clinical trials; analyse capability and make recommendation for trial inclusion
  • Assume ambassadorial role to facilitate communication between sites and Operations to increase value proposition to investigators
  • Facilitate preparation and collection of site level documents during all phases of the trial; resolve problems as required
  • Execute site initiation and training
  • Implement total site management including monitoring visits, regulatory assessment, drug supply management and resolution of site problems to ensure compliance
  • Identify problems at sites; resolve issues and escalate as appropriate
  • Collaborate with the clinical study manager (CSM) to ensure recruitment and execute contingency plans, as needed
  • Complete preparation and generation of study monitoring reports
  • Review and manage data remotely and at site; resolve technical and content issues on a continuous basis in order to achieve timely database lock targets
  • Implement site close-out activities.

Please contact Marc.Joseph@chiltern.com for further information on the role.

About Chiltern:

Chiltern is the leading, global mid-sized contract research organization that listens to client needs to deliver customized clinical development solutions. Chiltern’s team of more than 4,200 works across 47 countries to provide flexible, specialized services, with core competencies in Biopharma, Medical Device and Diagnostics, Oncology, Clinical Analytics and Source. Visit www.Chiltern.com to learn more about responsive solutions that are Designed Around You®.

key words clinical research associate, monitoring, monitor, CRA

 

 

Apply for this job: Clinical Research Associate

Contact Information:

Address:  London, UK
171 Bath Road Slough Berkshire
SL1 4AA, UK
England
Tel:  +44 (0) 1753 512000
Fax:  +44 (0) 1753 511116
Website:  Visit Our Web Site

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