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Ipsen Global

Global biopharma focused on specialty care

Head of Business Enablement and Compliance

Clinical Research OperationsPosted on Nov 10
Full-timeNo salary listedIn-person

About the Job

Requirements

  • At least 10 years of experience within the pharmaceutical, biotech, or related industry, with a track record of transformational leadership in a global cross-functional environment.
  • Experience in clinical development, clinical operations, quality, compliance, or related areas in the pharmaceutical or biotech industry.
  • Deep understanding of the clinical trial landscape and commitment to innovation, creativity, and operational excellence.
  • Extensive demonstrated knowledge of drug development processes, ICH-GCP guidelines, 21 CFR Part 11, and major health authority regulations.
  • Experience in audit and inspection readiness, preparation, and conduct.
  • Ability to provide visionary and strategic leadership.
  • Experience in large-scale organizational change management and implementation programs.
  • Proven ability to influence and drive change, with project management capabilities in planning, prioritization, problem solving, and organizational skills; ability to manage multiple priorities in a dynamic environment and an agile mindset.
  • Experience managing internal stakeholders and communicating across all organizational levels, including executive leadership.
  • At least 6 years of people or project management experience, such as leading project teams, operational teams, or cross-functional teams through operational change and transformation.
  • Extensive knowledge of Good Clinical Practice and related global regulatory and compliance requirements for clinical studies.
  • Strong understanding of clinical systems, including eTMF, CTMS, and QMS, and business process design.
  • Effective leadership skills and the ability to foster team productivity and cohesion in a changing environment.
  • Sound financial acumen.
  • A bachelor's degree in a scientific discipline or general management.
  • Fluency in English.

Responsibilities

  • Establish and continuously improve key capabilities for IPSEN, including a framework for internal business-process ownership, business management of key clinical systems, training, and compliance, in support of Clinical Development Operations and the broader organization.
  • Partner with R&D, Medical, and enabling functions such as IT and Quality to support clinical trial planning, execution, closeout, and site partnership and engagement.
  • Shape business-process and training strategies, train IPSEN staff and vendors, and maintain a culture and practice of inspection readiness.
  • Champion new ways of working across R&D and Medical, identifying opportunities and best practices to improve clinical development activities.
  • Provide strategic leadership to a multifunctional team, setting its vision, priorities, and expectations across compliance, training, systems support, and business-process ownership.
  • Coach, mentor, and develop team members, building functional expertise, accountability, and long-term talent development.
  • Create an inclusive, collaborative, high-performing team environment that encourages innovation, continuous improvement, and shared learning.
  • Contribute to CDO strategy, portfolio execution, and cross-functional decision-making as an active member of the senior leadership team.
  • Build partnerships with senior leaders across Clinical Development Operations, Quality, Medical, Regulatory, and Digital/Data organizations.
  • Lead or sponsor change initiatives to strengthen operational excellence and adoption of processes, systems, and ways of working across the global organization.
  • Own IPSEN’s Clinical Development SOP strategy with Global Quality, ensuring consistent standard practices across functions and teams, including GMA where applicable.
  • Create a plan for process management aligned with IPSEN’s move toward Functional Service Provision.
  • Establish a Business Process Ownership framework that clarifies SOP organization and enables effective use.
  • Ensure SOPs are fit for purpose and capture applicable corrective actions from audit findings.
  • Define SOP review and approval processes, and processes for SOP implementation and partnering.
  • Provide strategic oversight of clinical systems teams, including CTMS and TMF, ensuring the vision, roadmap, and integrations align with clinical operations strategy and the broader digital ecosystem.
  • Establish governance for cross-system integration, data stewardship, quality, and compliance in alignment with GxP and internal standards.
  • Oversee prioritization, resource allocation, and performance management for clinical platform evolution, ensuring stability, scalability, and long-term digital enablement.
  • Partner across Clinical Operations, Digital/Data, Quality, and IT to translate business needs into system capabilities, adoption strategies, and user-experience improvements.
  • Guide continuous improvement and digital transformation, including identifying AI and innovation opportunities, enhancing workflows and oversight, and strengthening the clinical systems ecosystem.
  • Oversee the design, governance, and continuous improvement of global role-based training curricula, onboarding programs, and competency frameworks.
  • Ensure Learning Management Systems and training processes meet compliance requirements, including GxP, inspection readiness, and auditable documentation standards.
  • Develop and execute training strategies for new systems, processes, and organizational changes, driving adoption and sustained performance improvements.
  • Partner with Quality and HR Learning teams to ensure training content is accurate, standardized, current, and effectively delivered across global teams.
  • Monitor training performance using metrics, dashboards, and compliance indicators to guide prioritization, resource allocation, and capability enhancements.
  • Build and mentor the Training team, fostering innovation, collaboration, and continuous learning.
  • Direct the Compliance team, monitoring compliance risks and ensuring mitigation and remediation plans are prioritized, resourced, and delivered.
  • Create and oversee frameworks for quality-control checks, compliance monitoring, and TMF and training-documentation reviews; ensure risk signals are escalated and addressed with timely corrective actions.
  • Guide the team in preparing for audits, inspections, and Quality Reviews, coordinating with clinical operations, quality, and regulatory partners.
  • Ensure strong CAPA governance by reviewing root-cause analyses, validating CAPA effectiveness, and fostering a consistent, risk-based approach across countries and studies.
  • Oversee the team’s assessment of local regulatory intelligence and procedural-document updates, including with CRO partners, and translate changes into operational guidance and quality-system updates.
  • Ensure effective onboarding and handover processes for CDO staff and contractors.
  • Enable a centralized system for storing and rapidly retrieving job descriptions, training files, and CVs as required under ICH-GCP, including periodic review for audit and inspection readiness.
  • Monitor emerging compliance concerns across CDO and review business and GCP policy and procedural deviations affecting CDO objectives.
  • Trend audit and inspection root-cause analyses across CDO, identify lessons learned, and drive review meetings to consider adjustments to operational procedures and training.

Desired Qualifications

  • An advanced degree, such as a Master's, MBA, MD, or PhD.

About the Company

Ipsen Global

Global biopharma focused on specialty care

Ipsen is a global biopharmaceutical company that concentrates on specialty care, developing and marketing medicines for oncology, neuroscience, and rare diseases. Its products work by treating specific high-need conditions, ranging from historical diarrhea treatment Smecta to modern targeted therapies in cancer and neurological disorders. The company differentiates itself through a focused portfolio in niche therapeutic areas, growth via strategic acquisitions, and a long-standing family heritage that shaped its international expansion and IPO-driven capital for expansion. Its goal is to address unmet medical needs worldwide by providing effective therapies for patients with serious or rare conditions.

Company size
5,001-10,000
Company stage
IPO
Headquarters
Boulogne-Billancourt, France
Founded
2005

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