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www.cvonline.hu

Regulatory Submissions Manager


  • A hirdetés 1007 napja lejárt

Location: Hungary
Office: Budapest
Full-time or Part-time: Full-time

 

Description

DESCRIPTION OF JOB DUTIES

  • Efficiently manage and successfully execute all aspects of global start-up according to Sponsor specifications;
  • Perform quality checks on submission documents and site essential documents;
  • Prepare and approve informed consent forms;
  • Review pertinent regulations to develop proactive solutions to start-up issues and challenges; and
  • Present during bid defenses, general capabilities meetings, and audits.
  • Line manage the regulatory submissions team.

 

QUALIFICATIONS/REQUIREMENTS

  • More than 5 years of experience in clinical research, preferably with a CRO. Experience may include CRA or project management experience;
  • Knowledge and experience with Clinical Trial Applications within Europe; and
  • Strong oral and written communication skills.
  • Fluency in English and local language.

Travel: Minimal


WHAT TO EXPECT NEXT

We look forward to receiving your application. A member of our recruitment team will review your qualifications. If interested, you will be contacted for an interview.

Please apply online at Link megjelenítése.

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