Senior CRA/Specialty Pharma/South East UK career at Applitracker in Uxbridge

Applitracker is employing Senior CRA/Specialty Pharma/South East UK on Sun, 08 Sep 2013 15:49:59 GMT. We currently have a new requirement for a SCRA. This is a full time position offering significant exposure to national and international clinical trials and monitoring. Role Our client is an exciting and dynamic specialty pharmaceutical company with trials in the Gastroenterology/GI space, currently offering a new opportunity for a seasoned Clinical Research Associate (CRA/SCRA). They require a...

Senior CRA/Specialty Pharma/South East UK

Location: Uxbridge England

Description: Applitracker is employing Senior CRA/Specialty Pharma/South East UK right now, this career will be placed in England. More complete informations about this career opportunity kindly see the descriptions. We currently have a new requirement for a SCRA. This is a full time position offering significant exposure to national and international clinical trials and monitoring.
Role

Our client is an exciting and dynamic specialty pharmaceutical company with trials in the Gastroenterology/GI space, currently offering a new opportunity for a seasoned Clinical Research Associate (CRA/SCRA). They require a Snr CRA level professional to join part of a growing team and be responsible for national an international monitoring of clinical trials in UK, Europe and potentially the US and RoW.

Essential Skills/Experience

  • BSc in life science or nursing qualification with minimum 3 years' experience in the healthcare sector (pharmaceutical, biotechnology, national healthcare or CRO) of which at least 1-5 years of which should be in a clinical trial monitoring role experience (at least 1 year for CRA role, >3 years for CRAII role and >5 years for SCRA role) and including pan-European experience.
  • Recent experience of coordinating other CRAs/CTAs in a pharma or CRO setting (SCRA role)
  • Strong attention t! o detail in clinical study implementation, with good working k! nowledge of ICH/GCP Guidelines.
  • Able to resolve routine issues independently. Must have demonstrated problem-solving abilities in overseeing clinical sites, and demonstrated tactfulness and diplomacy in dealing with study coordinators and physicians.
  • Ability to work in a team as well as independently
  • Good time management skills
  • Effective interpersonal skills
  • Good command of written and spoken English language
Desired Skills/Experience

  • Knowledge of gastroenterology, hepatology or cancer supportive care preferred
  • Some experience in the use of EDC and IXRS platforms
  • Some experience in study / site set up
  • Knowledge of requirements for ethics and regulatory approvals and other 'Green Light' documentation.
This opportunity is based out of our clients offices I South East of England, within commutable distance from West London. Our client is ideally looking for an indivi! dual to be based locally to their offices and work in-house when not monitoring, however this is negotiable.

For more information call Bernardo on (0) or alternatively send your latest CV to .

Join me on LinkedIn and keep up to date with my latest vacancies and industry news ch.linkedin.com/in/bernardoreveco
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If you were eligible to this career, please email us your resume, with salary requirements and a resume to Applitracker.

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

This career starts available on: Sun, 08 Sep 2013 15:49:59 GMT



Apply Senior CRA/Specialty Pharma/South East UK Here

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