Jobs at Ipsen

Leads clinical development strategy and execution for rare disease programs from early development through registration and launch. Supports clinical study teams, prepares and reviews development and trial documents, ensures data integrity and regulatory compliance, makes clinical decisions, manages cross-functional alignment, and engages investigators, key opinion leaders, regulators, CROs, and internal stakeholders. Also contributes medical expertise to preclinical development, competitive intelligence, external innovation, and business development activities.

Leads Ipsen’s AI Programming capability within Biometry, establishing strategy, standards, governance, and operating models for AI-enabled programming and automation. Manages clinical data scientists, AI programmers, and application developers while delivering ML, LLM, data products, and applications for clinical and R&D use cases. Partners across Biometry, IT, data and analytics teams, and external vendors to ensure validated, secure, scalable, reproducible solutions and drive organizational adoption.

Leads end-to-end Data, Analytics, and AI projects across business domains, from scoping and planning through delivery, adoption, and operational handover. Coordinates business, data, technology, security, compliance, and external partner teams while managing scope, budgets, timelines, risks, governance, requirements, and stakeholder communications. Ensures solutions meet business, data quality, privacy, security, and compliance expectations and contributes to improved project delivery standards.

Manage and improve enterprise endpoint platforms, including MECM, Intune, JAMF, Autopilot, imaging, software distribution, patching, encryption, mobile device management, and endpoint security. Provide third-level technical support, resolve escalated incidents, coordinate vendors and IT partners, advise internal teams, maintain security standards, and investigate opportunities for automation and improved reliability. The role also supports asset management, desktop virtualization, operational reporting, and enterprise Windows technologies.

Owns Ipsen’s enterprise Master Data Management strategy, platform roadmap, operating model, service delivery, data quality, integrations, vendor relationships, budget, and continuous improvement. The role leads global MDM transformation, governs backlogs and investments, supports analytics and AI enablement, ensures regulatory and privacy alignment, and partners with business, IT, architecture, data governance, and delivery teams to improve trusted master data adoption and business value.

Leads Ipsen’s statistical innovation strategy across R&D, including innovative trial design, simulation, advanced modeling, predictive analytics, digital twins, virtual controls, and data mining. Manages a specialist quantitative team, establishes methodological standards, supports regulatory and portfolio decisions, and partners with biostatistics, clinical development, data science, and other cross-functional groups. Develops talent, oversees reproducible and submission-ready methods, and builds external scientific networks.

Leads biostatistical strategy for neuroscience drug development programs, including study design, statistical analysis plans, regulatory submissions, clinical trial interpretation, and scientific publications. Oversees CROs and statistical providers, supports FDA, EMA, and PMDA interactions, advances adaptive and Bayesian methodologies, manages risks and resources, and mentors biostatistics staff. Requires strong expertise in clinical study designs, statistical programming, CDISC standards, SAS, R, and pharmaceutical development.

Develops omnichannel customer engagement strategies and journeys for healthcare professionals. Leads digital campaigns from planning and content deployment through measurement and optimization, partners with brand and medical teams, supports compliant digital content governance, uses analytics to improve performance, and leads digital transformation projects and capability rollouts.

Leads global oncology clinical development programs from strategy through execution, overseeing clinical operations, timelines, budgets, CRO and service-provider relationships, regulatory submissions, compliance, and cross-functional delivery. Manages and develops Clinical Project Managers, Clinical Monitoring Leads, and Clinical Trial Assistants while driving operational excellence, risk management, process improvement, and stakeholder engagement across global Phase 1–3 studies.

Leads end-to-end Clinical Development business processes, establishing strategy, governance, compliance controls, KPIs, systems integration, risk management, and continuous improvement. Coordinates stakeholders across clinical operations and R&D, monitors process performance, resolves escalations, supports training, and drives efficient, high-quality clinical development outcomes.

Leads pharmacy support for global clinical trials, serving as a subject matter expert on investigational product handling, preparation, administration, storage, accountability, hazardous drug management, and site readiness. Develops pharmacy training and guidance, supports quality and inspection readiness, manages pharmacy vendors and contractors, advises on CSTD implementation, and drives process improvements across oncology and other clinical development programs.

Leads cross-functional clinical study teams and CROs through global clinical trial setup, execution, and closeout. Manages timelines, budgets, vendors, feasibility, site selection, regulatory and safety requirements, quality oversight, patient recruitment, reporting, and clinical study documentation. Ensures compliance with GCP, SOPs, QMS, and applicable regulations while coordinating internal and external stakeholders and supporting inspections, audits, CAPA implementation, and clinical study report completion.

Oversee clinical contract compliance, data privacy, and GDPR requirements for clinical studies, registries, and managed access programs. Advise Clinical Operations teams on contracting and privacy matters, support compliant study execution, and oversee recruitment, onboarding, and training for the Clinical Contract Associate team.

Leads Western European country-cluster clinical operations across the full trial lifecycle, including feasibility, site selection, start-up, monitoring, recruitment, close-out, and inspection readiness. Oversees FSP partners, ensures ICH-GCP and regulatory compliance, manages internal clinical operations teams, drives site engagement, performance metrics, risk mitigation, and continuous improvement, and serves as the senior sponsor representative for country-level delivery and stakeholder relationships.

Leads clinical quality and compliance across Ipsen clinical trials, ensuring adherence to GxP standards, SOPs, regulations, and inspection requirements. Develops cluster quality plans, identifies and remediates compliance risks, oversees CAPAs and root-cause investigations, supports audits and inspections, governs procedural updates, assesses regulatory changes, and coordinates supplier quality activities. Partners with clinical operations, quality, and cross-functional stakeholders to maintain inspection readiness and drive continuous improvement.

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.

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.

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