Lead Clinical Trial Operations Manager Jobs in Frankfurt am Main

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Working Student (mfd) Global Regulatory Affairs

Merz Therapeutics

profile Frankfurt am Main - Germany

YOUR CONTRIBUTIONWithin our Global Regulatory Affairs departmentyou will support the implementation of our new DMS (Document Management System) by migrating data files. Together with you we will ensure our regulatory processes and contribute to the achievement of our corporate goals. We offer you ex...

30+ days ago
Part-Time

Local Contact Person For Pharmacovigilance And Reg...

Ergomed

profile Frankfurt am Main - Germany

The Local Country Person Responsible for Pharmacovigilance and Regulatory Affairs (LCPPV/LCPRA) serves as the primary local representative to ensure compliance with national pharmacovigilance and regulatory requirements. This dual-role position is responsible for executing PV and RA activities at th...

30+ days ago
Remote

Regional Regulatory Affairs Manager (mfd)

Merz Therapeutics

profile Frankfurt am Main - Germany

YOUR CONTRIBUTIONAs a Regional Regulatory Affairs Manager (m/f/d) you will provide regional regulatory support for the strategic development approval and life cycle management of drugs ensuring compliance with regulatory and legal requirements in the region APAC-MEA. This will include the following...

30+ days ago
Full Time

Team Lead Regulatory Affairs Regions (mfd)

Merz Therapeutics

profile Frankfurt am Main - Germany

YOUR CONTRIBUTIONIn the role ofTeam Lead Regulatory Affairs Regions (m/f/d) you contribute to the development and success of the Merz Therapeutics organization. You lead a team of 10 professionals ensuring timely and compliant execution of regional regulatory activities across the product lifecycle....

30+ days ago
Full Time

Regulatory Affairs Manager (mfd) Cmc

Merz Therapeutics

profile Frankfurt am Main - Germany

YOUR CONTRIBUTIONAs a Regulatory Affairs Manager (m/f/d) CMC you will apply your knowledge of global regulatory quality requirements to support the approval and maintenance of medicinal products. The position is limited to 3 years and includes the following activities:Create review and update high-q...

30+ days ago
Full Time