Company: Barrington James Clinical
Closing Date: 29 Oct 16
Salary (£): Competitive
Begin to progress your career the minute you start! With this niche opportunity you will be working in very new markets on the latest projects!
My client are actively expanding their clinical division and are looking for a new team member! If you are tired of feeling like you are not appreciated, not feeling like you are getting the progression you deserve and are not working on exciting projects then this is the opportunity for you! Working in late phase you will be in a niche role exploring new therapeutic areas while working on the very latest projects!
You have the choice of being officebased or homebased so either join the active social environment that is within the office or work from your home and be more relaxed!
Working independently and proactively to coordinate all necessary activities required for setting up and monitoring a study, completing accurate study status reports and maintaining study documentation. You will be involved in the submission of protocol, consent documents for ethics/IRB approval and assist in the preparation of regulatory submissions as requested.
Managing sponsor generated queries efficiently and taking responsibility for study cost effectiveness; you will also participate in the preparation and review of study documentation and feasibility studies for new proposals as required.
Depending on your level of experience, you may assist in training and mentoring less experienced CRA’s and/or manage CRA’s working on international projects.
2 years independent monitoring
Experience in late phase (phase IIII and IV)
To get in contact and hear more about this exiting and unique opportunity please email me - firstname.lastname@example.org
Or call me here at Barrington James +44 (0) 1293 77 66 44 and ask for Josh Chart.
I look forward to hearing from you!
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