München: Clinical Regulatory Affairs Manager (m/w)

An exciting opportunity has arisen to join a Munich office of a successful and fast-growing leading full‐service global contract research organization, specialized in clinical drug Development. Our client is seeking an experienced candidate for a new position:
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

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

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

Interested?
Please send your complete application to:
Silvio Di Meglio
CEO / Recruiter
Triga Consulting GmbH & Co. KG
Rablstr. 26 / 81669 München
Tel.: 0049-(0)89-80913072-1
dimeglio@triga-consulting.de
www.triga-consulting.de