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Manager Regulatory Affairs

Manager Regulatory Affairs

Manager Regulatory Affairs

Manager Regulatory Affairs

Proclinical Staffing

Pharma, Medizintechnik

Zürich

  • Art der Anstellung: Vollzeit
  • 78.000 CHF – 104.000 CHF (von XING geschätzt)
  • Vor Ort

Manager Regulatory Affairs

Über diesen Job

Manager Regulatory Affairs

Salary: Highly Competitive
  1. Job type: Contract
  2. Discipline: Senior/Director & VP
  3. Location: Switzerland
Zürich, Switzerland
Posting date: 12 Aug 2025
Reference: 66605
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Proclinical is seeking a Manager of Regulatory Affairs to support regulatory strategies and submissions for investigational applications, market applications, and life-cycle management in the gastroenterology and pharmaceutical sectors. This role involves collaboration with global, regional, and local teams to ensure patient access and compliance with applicable regulatory requirements.

Please note that to be considered for this role you must have the right to work in this location or hold an EU passport.

Responsibilities:

  • Contribute to the development and execution of regional regulatory strategies to maximize product success and patient access.
  • Collaborate with global, regional, and local teams to align program objectives and ensure timely approvals.
  • Lead or support submission working groups and represent the region on global and project teams as needed.
  • Support interactions with health authorities, including preparation for and participation in meetings.
  • Monitor and interpret regional regulations and guidance to assess their impact on drug development, registration, and life-cycle management.
  • Provide regulatory expertise throughout the product life cycle, including post-marketing compliance.
  • Develop and maintain effective working relationships with internal teams, consultants, and business partners.
  • Communicate regulatory strategies, submission plans, and timelines effectively to stakeholders.
  • Ensure regulatory submissions and approvals are achieved on schedule.
  • Support access initiatives by partnering with relevant functions to facilitate patient access strategies.

Key Skills and Requirements:

  • A degree in a scientific field (BSc required; advanced degree preferred).
  • Experience in drug regulatory affairs, particularly within the EU or emerging markets.
  • Familiarity with regulations governing drugs and biologics across all development phases.
  • Knowledge of advanced therapeutic medical products, such as cell and gene therapy, is advantageous.
  • Strong analytical skills with attention to detail and the ability to make reasoned recommendations.
  • Effective communication and relationship-building skills.
  • Adaptability to changing circumstances and the ability to manage multiple priorities.
  • Demonstrated ability to work inclusively and empathetically within diverse teams.

If you are having difficulty in applying or if you have any questions, please contact Ashley Bennett at a.bennett@proclinical.com.

Apply Now:

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.

Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.

By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data - https://www.proclinical.com/privacy-policy

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Proclinical Staffing

Personaldienstleistungen

51-200 Mitarbeitende

Frankfurt am Main, Deutschland

Bewertung von Mitarbeitenden

Gesamtbewertung

Basierend auf 7 Bewertungen

Vorteile für Mitarbeitende

Flexible Arbeitszeiten
Home-Office
Kantine
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Training
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Vorteile für Mitarbeitende
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