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Regulatory Affairs Assistant

PSI CROMunich, Bavaria, Germany

Vor 3 Tagen

Stellenbeschreibung

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

OfficeBased in Munich / Planegg

You will :

Be the point of contact for clinical project teams and support services on regulatory matters
Prepare draft regulatory / ethics submission dossier
Be responsible for document management such as filing processing translation 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 fulfil 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 youd 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 :

Fulltime

Key Skills

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

Experience : years

Vacancy : 1