Jobs at Ipsen

Leads global market access, reimbursement, pricing, and value strategies for Ipsen’s neuroscience portfolio. Develops payer value tools, supports HTA and evidence-generation activities, advises on pricing and business cases, and partners with global and affiliate teams to optimize patient access. Coordinates cross-functional initiatives, external consultants, and project delivery across international markets while monitoring payer requirements, healthcare systems, and competitive landscapes.

Leads global regulatory submission projects for marketing authorizations, new indications, and strategic filings. Develops integrated timelines, coordinates cross-functional deliverables, manages risks and dependencies, supports scenario planning, and ensures compliant, high-quality submissions across regions. Partners with Regulatory Affairs, Clinical, Quality, Manufacturing, and other stakeholders while driving communication, process improvement, and operational efficiency. Requires pharmaceutical regulatory submission experience, CTD knowledge, scientific education, strong project management skills, and fluent English.

Leads global regulatory submission projects for marketing authorizations, new indications, and strategic filings. Coordinates cross-functional teams, develops integrated timelines, manages risks and deliverables, supports scenario planning, and ensures compliant, high-quality submissions across regions. Requires pharmaceutical Regulatory Affairs experience, international CTD filing knowledge, drug development understanding, project management skills, and familiarity with eCTD publishing, RIMS, and regulatory technologies.

Leads global pharmaceutical pricing activities across products, regions, and countries. Manages price variation requests, coordinates stakeholders, performs international reference pricing and profitability analyses, maintains pricing data integrity, and supports global planning. Contributes to tiered pricing, value-based pricing, affordability, managed entry schemes, and broader pricing strategy while providing expertise to cross-functional projects.

Supports UK and Ireland regulatory lifecycle submissions, licence maintenance, regulatory changes, authority responses, and regulatory intelligence. Maintains regulatory databases and documentation while assisting with quality systems, change controls, deviations, CAPAs, complaints, inspection readiness, compliance reporting, and KPI generation. Collaborates with Medical Affairs, Pharmacovigilance, Quality, Supply Chain, Commercial, and Global Regulatory Affairs teams, with an initial focus on oncology products.

Administer and support Veeva CRM and Vault, managing users, configuration, governance, controls, issue resolution, training, and system enhancements. Partner with Sales, Marketing, Medical, Compliance, and global teams to improve omnichannel engagement. Develop KPI reports and insights using data to support decision-making, platform adoption, compliance, and continuous improvement across the UK and Ireland.

Lead design and delivery of global scientific training for medical affairs, build blended learning journeys using adult-learning principles, collaborate with regional medical teams, drive capability development, support MEGS training data, ensure compliance with SOPs, and provide global project leadership to enhance medical expertise and business outcomes.

Lead operationalization of global clinical development resourcing, budgeting, and performance reporting. Build resourcing tools, dashboards, and analyses to inform portfolio and capacity decisions, support CDO finance and governance, and coordinate Strategy & Operations activities and events.

The IT Strategic Enterprise Architect will define architecture foundations, develop enterprise application blueprints, and influence strategic technology decisions to enhance organizational value and clarity.

The Head of Safety Partnering is responsible for defining and leading Ipsen's global pharmacovigilance strategy, ensuring compliance and effective partnerships in the pharmaceutical industry.

Leads global pharmaceutical market research, performance analytics, forecasting, and business planning for strategic brands. Combines primary and secondary data, competitive intelligence, patient modeling, and market trends to guide brand strategy, sales ambitions, business cases, and portfolio decisions. Partners with Commercial, Medical Affairs, Market Access, Finance, R&D, affiliates, vendors, and senior stakeholders while maintaining analytics tools and knowledge-management resources.

Lead clinical QA oversight for Ipsen's clinical studies, ensuring GCP and regulatory compliance, inspection readiness, risk-based quality oversight, vendor oversight, investigations, CAPAs, and continuous improvement across clinical and medical quality systems.

Lead Global Regulatory Operations to define strategy, governance and capabilities for regulatory data, submissions, labelling and digital platforms. Drive transformation via AI, automation and data governance; ensure inspection readiness, deliver submission excellence, manage budgets, vendors and cross-functional stakeholder relationships while building a high-performing global team.

Lead enterprise Centralized Monitoring and RBM strategy across clinical development. Oversee CM teams and vendors, drive analytics and dashboards, set KRIs/QTLs, ensure inspection readiness, implement AI/automation, and provide governance, training and cross-functional oversight to protect patient safety and data integrity.

Lead and coordinate biomarker operational activities across clinical studies, focusing on tissue biomarkers and IHC. Manage biospecimen logistics, vendor oversight, assay implementation, documentation, quality and inspection readiness. Serve as SME for tissue biomarker workflows, collaborate with internal and external stakeholders, and drive process improvements and standardization across biomarker operations.

The Clinical Supply Chain Forecast Manager will drive supply forecasting for clinical programs, manage budget requirements, and ensure adequate clinical forecast estimates and supply continuity for studies, working with various cross-functional teams to align production and distribution needs.

Manage IMP design and global clinical supply chain strategy for clinical trials. Lead cross-functional teams, create project plans, align with regulatory/CMC, forecast and resupply materials, track KPIs and risks, handle quality events, and drive continuous improvement to ensure on-time patient supply.

The Executive Assistant will provide administrative and secretarial support to the Senior Vice President, managing logistics, travel, expenses, and documentation while ensuring effective coordination across teams and projects.

Lead global labelling strategy and lifecycle management (CCDS, USPI, SmPC/PIL) for assigned products, provide regulatory input into clinical development, oversee labelling negotiations with authorities, drive process improvement and digitalisation, mentor team members, and ensure consistent, compliant labelling across regions.

Lead a team of Global Events Excellence Project Managers to define and execute the global congress and events strategy, oversee logistics, budgets, contracts, vendor management, compliance with pharma regulations, and continuously improve processes to ensure flawless event delivery.