Jobs at Ipsen

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 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.

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.

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.

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 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.

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 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.

Partner with UK & Ireland commercial and leadership teams to provide financial insight, forecasting, budgeting, reporting, and investment decision support. Lead FP&A processes, support pricing and profitability analyses, ensure timely management and statutory reporting, collaborate on S&OP, drive finance process improvements and transformation, and maintain strong financial controls.

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

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.