Clinical Research Associate/ Clinical Research Scientist job at Axess Ltd in Belfast

Axess Ltd is employing Clinical Research Associate/ Clinical Research Scientist on Wed, 03 Apr 2013 12:21:50 GMT. JOB SUMMARY: Fantastic opportunity for a Clinical Research Associate/ Scientist who will monitor phase 1 studies in Northern Ireland. 6month contract. This is a field-based role which has the flexibility to work from home 2 - 3 days/week. BACKGROUND: Global Pharma PRIMARY DUTIES * Set-up and monitor clinical trials, including pharmacogenetic sub-studies at an allocated number of...

Clinical Research Associate/ Clinical Research Scientist

Location: Belfast Northern Ireland

Description: Axess Ltd is employing Clinical Research Associate/ Clinical Research Scientist right now, this job will be placed in Northern Ireland. More complete informations about this job opportunity kindly read the description below. JOB SUMMARY:
Fantastic opportunity for a Clinical Research Associate/ Scientist who will monitor phase 1 studies in North! ern Ireland. 6month contract. This is a field-based role which has the flexibility to work from home 2 - 3 days/week.

BACKGROUND:
Global Pharma

PRIMARY DUTIES

  • Set-up and monitor clinical trials, including pharmacogenetic sub-studies at an allocated number of investigational sites, within defined therapy area(s), ensuring adherence to local and corporate SOPs, code of practice and GCP/ICH guidelines
  • Determine the feasibility of conducting protocols with reference to study complexity, clinical facilities and potential for recruiting patients and site selection
  • Agree appropriate targets for projects with CSM and Field Team Manager
  • Ensure targets for patient recruitment, data and audit quality and site related milestones are achieved for local and corporate clinical trials
  • Participate fully as a member of the clinical project team for investigator selection, trial status and progress and therapy ! specific training and provide relevant feedback relating to CR! F design and other study related documentation as appropriate
  • Maintain up to date and accurate central investigator documentation
  • Track and manage trial related payments to investigational sites
  • Adopt new initiatives and procedures and provide feedback where appropriate, e.g. patient recruitment initiatives and effective use of SMOs
  • Collection and feedback of competitor intelligence to the evidence planning process
  • Appropriate Key Opinion Leader liaison
  • Maintain links with commercial colleagues to share information and maximise opportunities
  • Be responsible for own development including monitoring, technical and therapeutic knowledge and skills by attending training as appropriate and undertaking background reading
QUALIFICATIONS / EXPERIENCE REQUIRED:
  • Degree in life sciences, pharmacy, pharmacology, nursing qualifications or equivalent qualification
  • Evidence of ability to ! deliver above responsibilities, e.g. likely to include experience of set-up and monitoring of investigational sites in one or more phases of clinical research, across one or more therapy areas, and evidence of delivery to time- and quality-related milestones
TO APPLY:
For a confidential discussion please telephone Caitlin Davies at AXESS Limited on 020 8560 2300. To apply, please send your CV to jobs@axess.co.uk quoting reference EM5524

Only candidates with EU work authorisation will be considered.

Keywords:
Belfast, Northern Ireland, Phase 1, CRA, Clinical Research Scientist, Senior CRA, Junior PM, Clinical Research Associate

ABOUT AXESS:
AXESS has been operating since 1990
We are a recruitment business dedicated to the pharmaceutical industry, specialising in Medical Affairs, Regulatory Affairs & Clinical Development
We match professional candidates to the best permanent, contract and interim r! oles in the market
Visit us at URL removed
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If you ! were eligible to this job, please email us your resume, with salary requirements and a resume to Axess Ltd.

If you interested on this job just click on the Apply button, you will be redirected to the official website

This job starts available on: Wed, 03 Apr 2013 12:21:50 GMT



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