Jobs at Ipsen

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.

Lead statistical programming for multiple clinical studies, ensuring quality and timeliness of deliverables (tables, listings, figures, datasets, DEFINE.XML), oversee outsourced CRO work, support regulatory submissions and health-authority responses, implement SAS/CDISC standards, mentor teams, and drive process improvements.

Lead statistical programming for rare disease clinical studies: develop and QC SDTM/ADaM and analysis datasets, produce TLFs and Define.xml for regulatory submissions, manage CRO/vendors, coordinate with statisticians and data management, and ensure regulatory-compliant deliverables.

Lead development and execution of clinical biomarker strategies across oncology and rare disease programs. Define biomarker plans, select technologies, oversee assay development and validation, manage external labs/CROs, integrate biomarker data into clinical interpretation and regulatory submissions, and represent biomarkers on cross-functional teams to support development decisions from early phases through registration.

Manage clinical investigational medicinal product (IMP) design and global supply chain strategy for clinical trials. Lead cross-functional subteams, coordinate with clinical, CMC and regulatory stakeholders, develop project plans and forecasts, mitigate supply risks, track KPIs, manage quality events, and drive continuous improvement to ensure on-time patient supply.

Lead development of Ipsen's global feasibility and study planning capability. Build and manage a hybrid team, establish governance and data-driven methodologies, integrate analytics/AI and RWD into site/PI selection, enrollment forecasting and operational plans, optimize protocol design, and maintain a centralized knowledge base and KPIs to continuously improve clinical trial feasibility, activation, and enrollment performance.

The role involves leading programming teams in biometry, developing technical solutions, ensuring regulatory compliance, and driving digital transformation in clinical data analysis.

The Director will lead the integration of new clinical assets, oversee clinical operations during transitions, and ensure compliance with regulatory standards.

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.

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 Global IT Operating Excellence Leader will enhance IT governance, optimize investments, implement vendor strategies, and ensure alignment with business priorities.

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

Field-based Key Account Manager responsible for building trusted relationships with oncology and urology stakeholders, delivering compliant disease and product information, securing formulary inclusions, and executing strategic territory and account plans. Collaborates with Medical, Marketing and Sales teams to drive account success; requires significant travel across the Northeast Midlands and East of England.

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.

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.

The Head eTMF Systems oversees Ipsen's eTMF ecosystem, managing compliance, system performance, and strategic operations while collaborating across departments to ensure quality and efficiency.

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.