Regulatory Affairs Assistant

Join our international team and support regulatory aspects of clinical research projects, streamlining communication, maintaining electronic systems, and managing documents.

Office Based in Munich / Planegg

You will:

• Be the point of contact for clinical project teams and support services on regulatory matters.
• Be responsible for document management such as filing, processing, translation, and quality control.
• Update and maintain (automated) tracking systems, working files, and schedules.
• Organize meetings, prepare agendas, and minutes.

Qualifications:

• College/University degree or an equivalent combination of education, training & experience.
• Life Science degree is a plus.
• Administrative work experience, preferably in an international setting.
• Prior experience in Clinical Research is a plus.
• Full working proficiency in English and German.
• Proficiency in MS Office applications.
• Ability to plan, multitask, and work in a dynamic team environment.
• Communication and collaboration skills.

Additional Information:

Start your career in clinical research coordinating a variety of tasks and learning new things while growing with the company.

Our extensive onboarding and mentorship program will prepare you to fulfill your tasks with the highest standards, offering you:

• Excellent and flexible working conditions.
• A unique combination of team collaboration and independent work.
• Competitive salary and benefits package.

If you would like to hear more about PSI, our organic growth and company culture, and learn more about the studies that we run and our high repeat and referral business rates, please apply for this vacancy.

Remote Work: Employment Type:

Key Skills:

Computer, Anti Money Laundering, ASP.NET, Advisory, IT Support, Maintenance Engineering

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