Jobs at Ipsen

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.

This role leads the customer experience data and automation strategy, ensuring scalable, compliant engagement and efficient measurement across markets.

The Clinical Development Director provides leadership and medical expertise in the design and execution of clinical development strategies and trials, ensuring compliance with regulations.

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 risk-based GCP/GCLP audits across internal and external partners, manage audit planning, execution, reporting and CAPA oversight, advise stakeholders and support inspections, coach and peer-review auditors, and collaborate globally within the audit team. Significant international travel required.

Lead end-to-end planning and execution of global congresses and events for a pharma company. Manage cross-functional teams, vendors, budgets, contracts, compliance, and post-event reviews while driving continuous improvement and stakeholder alignment.

Lead Ipsen's global public affairs and policy strategy for Neurosciences. Develop policy agendas, engage stakeholders (patient groups, clinicians, institutions), design multistakeholder initiatives, support brand and market access teams, run advocacy campaigns, monitor KPIs, and represent Ipsen externally to advance access and system-level change for stroke, spasticity, and migraine.

Lead biostatistics for oncology programs, providing program-level statistical strategy, study design, analysis, regulatory submissions, CRO oversight, and mentorship. Author and review protocols, SAPs, datasets, and clinical reports; apply advanced and adaptive statistical methods; ensure CDISC compliance; collaborate across R&D, regulatory, and external stakeholders to support drug development and scientific publications.

Lead Ipsen's global operations for clinical study management and site monitoring, ensuring strategic oversight, compliance, and high performance across trials globally.

The Clinical Supply Chain CDMO Project Manager oversees outsourced clinical packaging and distribution, ensuring compliance with regulations, effective vendor collaboration, and project management for clinical trials.

Temporary Global Marketing Director (maternity cover) responsible for defining and executing global brand strategy, leading launch and lifecycle marketing, developing omnichannel communications, driving market insights and forecasting, setting KPIs, coordinating with affiliates and agencies, and ensuring compliance with SOPs and ethics. Works cross-functionally with Medical, HEOR/Market Access, Decision Support and local teams to support global and local launches.

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.

Lead CMC regulatory strategy and dossier preparation for assigned products across development phases and lifecycle management. Manage regulatory interactions with health authorities, CMOs, alliance partners and internal stakeholders; coordinate CMC input for CTAs/MAAs, oversee eCTD-compliant submissions, risk/gap analyses, trackers and KPIs, and coach junior colleagues. Ensure global regulatory requirements (US, EU, JP, China, etc.) are met and propose de-risking or accelerated pathways.