Clinical Trial Assiociate

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Irfa******

  • Netherlands Antilles 
  • Last Update: 10.06.2019 at 12:00

Job Type
Full Time
Start
ASAP
Duration
6 Month +
Place
Amsterdam, NL
Country
Netherlands Antilles

Category


Research Positions

Description


The Main Tasks Of The Project Specialist Are

  • Manage global contracting, funds and payments
  • Manage trial documents and data
  • Manage Investigator Sponsored (ISR) concept submissions and Request for Proposal
  • Generate / develop necessary metrics reports
  • Manages and prioritizes other activities as requested by the team (e.g., create documents/tools for team collaboration, planning meetings, mass mailings, postings on SharePoint etc.) related to MDO managed research
  • Evaluate which tasks to delegate to MDO Administrative staff

Relevant bachelor/master degree

  • Two years of equivalent relevant work experience. Experience in a pharmaceutical setting preferred
  • Must be self-directed, capable of making independent decisions and must possess effective verbal and written communication
  • Candidate must demonstrate teamwork, flexibility, time management and a strong work ethic
  • Extensive experience using computer and standard business software applications (i.e.,word processing, graphical presentations, spreadsheet analytics)

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