Manager Global Regulatory Affairs

vor 17 Stunden


Frankfurt am Main, Hessen, Deutschland Discover International Vollzeit

Job Overview

We are seeking an experienced Regulatory Affairs Manager to join our Global Regulatory Affairs team, supporting the development of small molecule drug products across clinical development phases I–III. This role will play a key part in shaping and executing global regulatory strategies to enable efficient clinical development and timely progression of assets.

Key Responsibilities

  • Develop and implement global regulatory strategies for small molecule products across Phases I–III
  • Lead regulatory activities for clinical development programs, including IND/CTA submissions, amendments, and lifecycle management
  • Act as the regulatory lead on cross-functional development teams, providing strategic guidance to R&D, Clinical, CMC, and Quality functions
  • Prepare, review, and manage high-quality regulatory documentation (e.g., briefing documents, investigator brochures, clinical trial applications)
  • Interface with global health authorities (e.g., EMA, FDA, other regional agencies) and support regulatory meetings and interactions
  • Monitor and interpret evolving global regulatory requirements and assess impact on development programs
  • Support regulatory intelligence activities and contribute to risk assessment and mitigation strategies
  • Ensure compliance with applicable regulatory guidelines, internal procedures, and timelines

Qualifications & Experience

  • University degree in Life Sciences, Pharmacy, Chemistry, or a related field (advanced degree preferred)
  • 5+ years of experience in Regulatory Affairs within the pharmaceutical or biotech industry
  • Strong experience with small molecule drug development
  • Proven hands-on experience supporting clinical development Phases I–III
  • Solid knowledge of EU and global regulatory frameworks
  • Experience working in global, cross-functional teams
  • Strong project management, communication, and stakeholder-management skills
  • Fluency in English (German is an advantage but not required)


  • Frankfurt am Main, Hessen, Deutschland IFRS Foundation Vollzeit

    Location: Frankfurt or London. The IFRS Foundation operates under a multi-location operating model; morning and evening calls will occur occasionally. Duration: month contract Reports to:      Director of Regulatory Implementation Job purpose:  The Regulatory Affairs Manager plays a key role in the design, development and delivery of an effective...


  • Frankfurt am Main, Hessen, Deutschland Triga Consulting GmbH & Co KG Vollzeit

    Für die Arzneimittelzulassung eines international tätigen biopharmazeutischen Unternehmens sucht TRIGA Verstärkung.Der Schwerpunkt des Unternehmens liegt auf der Entwicklung, Herstellung und Vermarktung biopharmazeutischer Humanarzneimittel mit Fokus auf Biosimilars.Der Arbeitgeber ist global organisiert und in zahlreichen internationalen Märkten aktiv....


  • Frankfurt am Main, Hessen, Deutschland TRIGA Consulting GmbH & Co. KG - Internal Vollzeit

    Für die Arzneimittelzulassung eines international tätigen biopharmazeutischen Unternehmens sucht TRIGA Verstärkung.Der Schwerpunkt des Unternehmens liegt auf der Entwicklung, Herstellung und Vermarktung biopharmazeutischer Humanarzneimittel mit Fokus auf Biosimilars.Der Arbeitgeber ist global organisiert und in zahlreichen internationalen Märkten aktiv....


  • Frankfurt am Main, Hessen, Deutschland IQVIA Vollzeit

    Shape the future of regulatory excellence at IQVIAAt IQVIA, we work to advance healthcare by helping our clients bring safe, effective medicines to patients. As a Regulatory Affairs Specialist, you will play a key role in ensuring compliance and supporting successful product lifecycle management across Germany, Switzerland, and Austria. You'll collaborate...


  • Frankfurt am Main, Hessen, Deutschland curasan AG Vollzeit

    Für unseren Standort in Frankfurt am Main (vor Ort / hybrid) suchen wir zum nächstmöglichen Zeitpunkt eine/n:REGULATORY AFFAIRS MANAGER / TECHNICAL DOCUMENTATION (M/W/D)Ihre Aufgaben umfassen:Bearbeitung, Aufrechterhaltung und Koordination der technischen Dokumentation für nationale und internationale Medizinproduktezulassungen, gemäß der...


  • Schwalbach am Taunus, Hessen, Deutschland Clinigen Vollzeit

    Clinigen is a rapidly growing global specialty pharmaceutical services business with a unique combination of services across the pharmaceutical lifecycle. We currently have over 1,000 employees headquartered in the UK with global offices in the US, EU (Belgium, Germany, France), Asia Pacific and South Africa. Clinigen is growing rapidly and is positioned...


  • Frankfurt am Main, Hessen, Deutschland The businesses of Merck KGaA, Darmstadt, Germany Vollzeit

    Your roleAn exciting opportunity has emerged for a Global Regulatory Project Manager (f/m/div) within the Regulatory Excellence & Strategy group in Life Science at Merck KGaA, Darmstadt, Germany. In this role, you will leverage your strong project management expertise to solve complex regulatory challenges and orchestrate cross‑functional collaboration...

  • Global Regulatory Lead

    vor 2 Wochen


    Frankfurt am Main, Hessen, Deutschland Merz Vollzeit

    YOUR CONTRIBUTIONJoin our motivated team in Global Regulatory Affairs and grow with exciting challenges. As Global Regulatory Lead(GRL) you are the primary interface and key strategic partner to Global Product Team (GPT) of throughout the product life cycle on New Assets and it's maintenance. This will include the following activities:Shaping regulatory...

  • Global Regulatory Lead

    vor 2 Wochen


    Frankfurt am Main, Hessen, Deutschland Merz Therapeutics Vollzeit

    YOUR CONTRIBUTIONJoin our motivated team in Global Regulatory Affairs and grow with exciting challenges. AsGlobal Regulatory Lead(GRL) you are the primary interface and key strategic partner to Global Product Team (GPT) of throughout the product life cycle on New Assets and it's maintenance. This will include the following activities:Shaping regulatory...


  • Frankfurt am Main, Hessen, Deutschland Merz Therapeutics Vollzeit

    YOUR CONTRIBUTIONIn the role of Team 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. You drive process optimization and collaborate closely...