Global Regulatory Pre-Award Strategy Director

Worldwide Clinical Trials is a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence. We are a worldwide team of over 3,500...

Almirall SA in Sant Feliu de Llobregat seeks an experienced Associate Director, Regulatory Affairs to lead global regulatory strategies and submissions for our dermatology portfolio.You will collaborate with Clinical, CMC, Safety and Market Access teams, coordinate CTAs, MAAs, variations, and renewals, and interact with health authorities to ensure timely...

AstraZeneca plc in Barcelona is seeking an Associate Director/Director, Clinical Regulatory Writing to lead pivotal CVRM submission content and strategy. You will mentor teams, shape submissions from development through approval, and drive best-in-class regulatory communications with senior stakeholders.You will guide cross-functional authoring groups,...

A leading consulting firm is seeking a Global CMC Regulatory Affairs Manager Consultant to support a top pharmaceutical company in Barcelona. This role offers the opportunity to provide regulatory insight, author CMC documents, and coordinate activities for market expansion. The ideal candidate will have at least 5 years of experience in regulatory affairs,...

Aim high, go beyond!At Open Cosmos we are solving the world’s biggest challenges from space, providing businesses, governments and researchers access to more readily available information than ever before - ready for the challenge? Then read on…The Satcom team is responsible for the design, delivery and performance of Open Cosmos’ satellite...

Alexion Pharma Spain S. L. is seeking an Associate Director, Global Health Economics & Outcomes Research to lead the strategy and execution of HEOR activities across a portfolio of diseases, assets and indications, to support worldwide launch and reimbursement. You will partner with Global Value, Access & Pricing, Medical, R&D, Regulatory and Commercial...

Page Executive is seeking a senior Regulatory Affairs professional to shape strategic regulatory initiatives for an expanding pharmaceutical portfolio. You will lead international registrations and lifecycle management, coordinating with R&D, Quality, Medical Affairs, and commercial teams to drive timelines and compliance. The role offers the opportunity to...

Job Title: Director, Regulatory Affairs Strategy - Cell Therapy Available locations: Barcelona, SpainAmsterdam, NetherlandsIntroduction to role: Are you ready to steer global regulatory strategy for cell therapies that redefine standards of care for patients? In this Director role, you will shape the regulatory path for programs that span oncology,...

Director, Global Oncology Data Strategy Location: Barcelona – Spain (3 days working from the office and 2 days working from home) The Centre for Oncology Data Excellence (CODE) is a team within Global Medical Evidence Generation organization that is focused on delivering best‑in‑class, scientifically rigorous research to support Global Medical Affairs...