Nymphenburger Str.120, 80636 München+49 (0)89 80913072-0info@triga-consulting.de
Contact info
Nymphenburger Str.120, 80636 München+49 (0)89 80913072-0info@triga-consulting.de

München: Clinical Regulatory Affairs Manager (m/w) | Pharma | Festanstellung

An exciting opportunity has arisen to join a Munich office of a successful and fast-growing leading full‐service global CRO, specialised in clinical drug
Development. Our client is seeking an experienced candidate for a new position:
Clinical Regulatory Affairs Manager (m/w)
We offer:

  • Excellent working conditions in a new office
  • Extensive training and friendly team
  • Competitive salary and benefits package
  • Opportunities for personal and professional growth

Job description:

  • cooperation with project teams to procure documents necessary for regulatory and ethics committee submission
  • preparation of regulatory and ethics committee submission dossiers, including import and export licenses
  • tracking regulatory project documentation flow and progress reporting
  • contact person for ethics and regulatory authorities and regulatory project teams
  • develop and implement corporate quality control tools and techniques pertaining to Regulatory Affairs
  • training company employees in regulatory issues

 Requirements:

  • technical expertise in managing regulatory aspects of clinical studies in Germany and EU
  • about 2-5 years of Regulatory Affairs experience and knowledge of the local regulatory environment
  • Scientific degree in biotechnology, biochemistry, cell biology or equivalent
  • Strong interpersonal, organizational and communication skills
  • excellent command of English and German

Interested?
Please send your complete application to:
Silvio Di Meglio
CEO / Recruiter
Triga Consulting GmbH & Co. KG
Nymphenburger Str. 120 / 80636 München
Tel.: 0049-(0)89-80913072-1
dimeglio@triga-consulting.de
www.triga-consulting.de
 

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