Regulatory Affairs Specialist (m/w/d) - Teilzeit

Regulatory Affairs Specialist (m/w/d)

This position is to be filled part-time.
 

 This tasks are awaiting you:

• Preparing ethics committee and regulatory submission packages according to relevant polish regulatory requirements;
• Collecting and updating information on EC and regulatory requirements;
• Filling, tracking, preparing and maintaining trial documentation
• Carrying out these duties, you will be fostering close contact with sponsors and site investigators

 

What you need to get started:

• Minimum of two years of experience in the clinical trials regulatory field, with a good grasp of regulatory guidelines of clinical trials conduct in Germany
• Very good organizational skills and attention to details
• Ability to work to tight deadlines and to prioritise workload in a fast-moving environment
• Excellent interpersonal skills and strong client service mentality
• Self-motivated and proactive, with ability to work across multinational teams
• Good oral and written communication skills in English and German
• Demonstrable ability to analyse and evaluate complex information
• Degree in life science or business

 
Your contact person for this position is Frau Franziska Mayr
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