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Regulatory Affairs, Pharmacovigilance Manager

Worldwide Salaried Open

Job Description:

  • Support the development and execution of regulatory strategies for Expanded Access Programs (EAPs) involving biologicals, cell therapies, and synthetic drugs.
  • Act as the Regulatory Affairs and Pharmacovigilance expert for communications with clients (pharmaceutical companies) and submissions to Health Authorities, as well as cross-functional meetings and audits.
  • Prepare, compile, and submit regulatory dossiers for cohort and named patient Expanded Access Programs (EAPs) on behalf of clients.
  • Provide input and support for the regulatory strategy for setting up and executing EAPs (e.g., where, when, and how).
  • Collaborate with the Commercial team to support new EAPs.
  • Ensure timely and compliant handling of all regulatory and pharmacovigilance activities related to EAPs.
  • Stay up to date on relevant global laws, regulations, and guidelines impacting EAPs.
  • Assist in drafting, reviewing, and maintaining regulatory documentation and templates.
  • Liaise with the Pharmacovigilance service provider to ensure alignment and compliance.
  • Contribute to maintaining department documentation such as SOPs (Standard Operating Procedures), QIs (Quality Incidents), and CAPAs (Corrective and Preventive Actions).

Requirements:

  • Approximately 5 years of relevant experience in Regulatory Affairs, including experience in Expanded Access.
  • Working knowledge of fundamental principles of Pharmacovigilance is required.
  • Solid understanding of national and international legislation and regulation relating to Expanded Access
  • A Bachelor’s or Master's degree in Life Sciences or a related field
  • Experience working directly with clients or external stakeholders in a professional setting
  • Strong communication skills (written and verbal) in English; able to convey complex topics clearly to both internal teams and external parties. Knowledge of additional languages is a plus
  • Comfortable collaborating across teams and working in a cross-functional environment
  • Proactive problem solver with the ability to identify potential regulatory or operational challenges early and suggest practical solutions
  • Familiarity with Microsoft 365 tools (e.g., Word, Excel, Teams, SharePoint)

Benefits:

  • Impactful work that helps patients gain access to potentially lifesaving treatments.
  • International work environment, scale-up energy and flat organizational structure which encourages creativity and accountability.
  • Competitive salary, annual performance bonus and an Employee Stock Option Plan.
  • Great career development opportunities in a fast-growing company.
  • Learning and development budget alongside internal knowledge sharing sessions.
  • Hybrid working model if you're in the Netherlands.
  • Policies to support working parents.
  • Healthy lunch at the thriving Amsterdam office.
  • Unlimited access to professional guidance by certified psychologists via OpenUp
  • Enjoy monthly events hosted by our vibrant Culture Club as well as an annual ‘myTomorrowland’ company-wide celebration!

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