Senior Manager, Clinical Data Standards

About Ipsen:

Ipsen is a mid-sized global biopharmaceutical company with a focus on transformative medicines in three therapeutic areas: Oncology Rare Disease and Neuroscience. Supported by nearly 100 years of development experience with global hubs in the U.S. France and the U.K we tackle areas of high unmet medical need through research and innovation.

Our passionate teams in more than 40 countries are focused on what matters and endeavor every day to bring medicines to patients in 88 countries. We build a workplace that champions human-centric leadership and fosters a culture of collaboration excellence and impact. At Ipsen every individual is empowered to be their true selves grow and thrive alongside the companys success. Join us on our journey towards sustainable growth creating real impact on patients and society!

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Job Title:

Senior Manager Clinical Data Standards

Division / Function:

Data Management Systems and Standards

Location:

Paris (FR) or London (UK)

WHAT - Summary & Purpose of the Position

The Senior Manager Clinical Data Standards will lead the strategic development implementation and governance of clinical data standards across the Research & Development division. This role ensures compliance with CDISC standards (CDASH SDTM ADAM) and global regulatory requirements supporting consistent high-quality data from collection through to submission-ready databases.

As a senior leader the Senior Manager will drive cross-functional collaboration oversee external service providers and mentor internal teams to foster excellence in data standardization. The role also includes active engagement with external industry groups such as the CDISC user community participation in regulatory forums and attendance at scientific congresses. These interactions support thought leadership ensure alignment with evolving standards and bring innovative practices back into the organization to continuously improve data quality and operational efficiency.

WHAT - Main Responsibilities & Technical Competencies

• Strategic Leadership & Governance
  • Define and drive the clinical data standards strategy aligned with regulatory and scientific requirements.
  • Establish governance frameworks for standards development approval and lifecycle management.
  • Lead gap analyses and impact assessments of evolving CDISC and regulatory standards.

• Cross-functional Collaboration
  • Partner with stakeholders across Medical Global Patient Safety Early Development Biostatistics and Clinical Operations to ensure harmonized data collection practices.
  • Promote adoption of standards through training communication and change management initiatives.

• Oversight of Service Providers
  • Manage and oversee external vendors responsible for the implementation and maintenance of data standards including budget review
  • Ensure timely delivery quality and compliance of vendor outputs through KPIs and performance reviews.

• Operational Excellence
  • Guide the design of CRFs edit checks derivations and metadata in EDC systems (e.g. RAVE) with according to best practices in the industry.
  • Support development of submission-ready datasets (SDTM ADAM).
  • Drive the development and maintenance of metadata repositories and standard libraries.
  • Manage the implementation of training programs related to clinical data standards including the development of materials and coordination of sessions to ensure consistent and effective knowledge transfer across functions.

• Leadership and Mentoring
  • Provide leadership and guidance to internal data standards team members and contributors.
  • Mentor junior staff and foster professional development through coaching feedback and knowledge sharing.
  • Champion a collaborative and inclusive team culture that supports innovation and continuous improvement.

• Innovation and Continuous Improvement
  • Identify opportunities to enhance data standardization processes through automation and technology.
  • Stay abreast of industry trends and contribute to internal innovation initiatives.
  • Engage with external industry groups such as the CDISC user community attend relevant regulatory agency forums and participate in scientific congresses to stay informed of emerging trends and bring innovative practices back into the organization

HOW - Knowledge & Experience

Knowledge & Experience (essential):

• Minimum 810 years of experience in clinical data management or standards
• Deep understanding of CDISC standards (CDASH SDTM ADaM) and global regulatory requirements.
• Proven experience in vendor oversight and cross-functional collaboration.
• Strong project management communication and stakeholder engagement skills.
• Experience with metadata repositories EDC systems (e.g. Rave) and data governance tools.
• Good knowledge of the drug development processes and the biometry processes
• Strong interpersonal and influencing skills with a collaborative mindset and ability to build positive relationships across diverse teams and stakeholders.
• Excellent communication abilities both oral and written with a focus on clarity accuracy and customer orientation.
• Proactive and supportive attitude demonstrating reliability teamwork and a commitment to helping others succeed in a matrix environment.

Knowledge & Experience (preferred):

• Minimum 3 year of experience in a leadership role
• Good level of expertise in the use of the data management and statistic software
• Familiarity with validation tools (e.g. Pinnacle 21) and submission processes.
• Familiarity with Non-clinical Data Standards (SEND)

Education / Certifications (essential):

• Advanced degree in Life Sciences Data Management Information Technology or related field.

Education / Certifications (preferred):

• CDISC (CDASH SDTAM) certifications

Language(s) (essential):

• English (Fluent)

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