Regulatory Affairs Manager (Global Clinical Trial Applications)

Thermo Fisher Scientific • Remoto

Publicado em 29/04/2026 às 10:41

Full-time Transportes/Logística Remoto
Salário €880
Descrição da Vaga

Work Schedule

Standard (Mon-Fri)Environmental Conditions

OfficeJob Description

At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life—enabling our customers to make the world healthier, cleaner and safer. With clinical trials conducted in 100+ countries and ongoing development of innovative frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services.

We are currently seeking a Regulatory Affairs Manager to join our global Regulatory Affairs department, Regulatory Science team. This is a fantastic opportunity to further develop your regulatory career and expertise in a global clinical trial setting.

In this role, you will be part of a global team providing innovative regulatory solutions, owning regulatory affairs responsibilities, and leading discussions with internal and external clients. You will coordinate global regulatory strategies on assigned (Phase 1–4) clinical trials, studies, and projects, supporting clients with strategic regulatory intelligence and guidance throughout clinical development.

Role Focus at This Level

  • This position sits within our senior individual contributor framework
  • In this Manager role, the emphasis is on oversight across multiple projects, client engagement, and accountability for delivery, scope, and financial elements.

Responsibilities

  • Lead the preparation of global regulatory submissions for CTA and ensure high quality standards that meet local and regional requirements.
  • Act as subject matter expert in providing regulatory strategy advice and technical expertise to internal and external clients and for key client projects of moderate to high complexity.
  • Provide oversight across multiple studies/projects, ensuring alignment of regulatory strategy, quality, and delivery.
  • Act as a senior client-facing lead, contributing to broader regulatory planning and supporting proposals, bid defenses, and scope discussions.
  • Ensure quality performance for key/managed projects.
  • Manage project budgeting/forecasting functions and maintain accountability for financial and scope management.
  • Identify and recognize out-of-scope activities and partner with relevant teams to manage contract modifications.
  • Collaborate with business development in pricing and securing new business by contributing to proposals, budgets, and client presentations.
  • Provide matrix/project leadership and guidance to team members.
  • Ensure compliance with relevant organizational and regulatory SOPs and WPDs.

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