Regulatory Affairs Manager

Basel  ‐ Onsite
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Description

Global Program Regulatory Manager with profound knowledge in Clinical Trial Applications (CTA) wanted for our Basel based client in the pharmaceutical industry.

Your experience/skills:
  • Relevant science based university degree
  • 2+ years' working experience in the field of regulatory management
  • Profound project management knowledge with proven ability to manage several projects and competing priorities
  • Expertise in regulatory operations as well as planning and compilation of CTAs with special focus on European submissions
  • Languages: fluent English both written and spoken


Your tasks:
  • Supporting the team in planning and tracking meetings and deliverables to support regulatory submissions
  • Assisting regulatory lead in the preparation and submission of global original Clinical Trial Applications (CTA)
  • Maintaining regulatory submission packages such as substantial amendments, DSURs and Investigator Brochures
  • Evaluating regulatory implication of non-clinical and clinical data as well as providing strategic regulatory input into selected clinical trials documents


Start: ASAP
Duration: 6MM+
Location: Basel, Switzerland
Ref.Nr.: BH12424

Does this sound like an interesting and challenging opportunity to you? Then take the next step by sending us your CV as a Word document and a contact telephone number.

Due to work permit restrictions we can unfortunately only consider applications from EU or Swiss citizens as well as current work-permit holders for Switzerland.

Going the extra mile…

New to Switzerland? In case of successful placement, we support you with:
  • All administrative questions
  • Finding an apartment
  • Health - and social insurance
  • Work permit and much more
Start date
03/2018
From
RM Group
Published at
16.02.2018
Project ID:
1504740
Contract type
Freelance
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