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Clinical Study Start up specialist Madrid

Permanent / Spain

from

Study Start up Specialist - office based Madrid

Our client is one of the best CRO on a global level, currently supporting Pharma and Biotech companies on a variety of Global trials from Phase I - Phase IV. They are currently expanding the team in Madrid and are looking for Study start up Specialists to work office based inMadrid.

Responsibilities

  • Responsible for start-up activities
  • Collecting documents from sites and review
  • EC submissions
  • Contract negotiations
  • Collaborate with site staff regarding patient recruitment
  • Collect Confidentially Agreements

Requirements

  • Previous experience as CRA/ inhouse CRA or Clinical Regulatory Specialist
  • Bachelor degree
  • Good written and verbal communication skills
  • Excellent knowledge of Microsoft Word, Excel, PowerPoint, Outlook
  • Fluent in Spanish and English language
  • Desirable knowledge of Portugese language

 

keywords - ec submissions/ ca submission, cta , clinical trial applications, regulatory specialist, start up specialist, country submission associate, regulatory coordinator

If you have difficulty in applying, have any questions or you cannot find what you are looking for please contact us on 0044 (0) 207 421 0000 or email info@life-science.co.uk. We regard all communication and correspondence as confidential. Full job descriptions are available on request.

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About us

Resourcing Life Science is a specialist recruitment agency, providing career advice and employment opportunities within the Pharmaceutical, Biotechnology, Medical Devices and Clinical Research industries across the globe.

Contact

info@life-science.co.uk

0044 (0) 207 421 0000

Resourcing Life Science Ltd.
226 High Road
London
NW10 2NX