Senior Manager, Clinical Data Standards

Ipsen Pharma (SAS); Paris; Hybride; EUR 80 000 - 100 000; Plein temps

Résumé du poste

A global biopharmaceutical company is seeking a Senior Manager for Clinical Data Standards in Paris. This role involves leading strategic development, implementation, and governance of clinical data standards, ensuring compliance with CDISC standards while managing external providers and fostering collaboration across functions. Ideal candidates will have extensive experience in clinical data management, strong project management skills, and a commitment to quality and innovation.

Prestations

Collaborative work culture

Professional development opportunities

Focus on innovation and inclusion

Qualifications

• Minimum 8–10 years of experience in clinical data management or standards.
• Deep understanding of CDISC standards (CDASH, SDTM, ADaM) and global regulatory requirements.
• Experience with EDC systems and vendor oversight.

Responsabilités

• Lead the strategic development and governance of clinical data standards.
• Manage external vendors for data standards implementation.
• Drive cross-functional collaboration and promote adoption of standards.

Connaissances

Clinical data management

Project management

Stakeholder engagement

Team leadership

Interpersonal skills

Communication (oral and written)

Formation

Advanced degree in Life Sciences

Outils

EDC systems (e.g., RAVE)

Metadata repositories

Data governance tools

Description du poste

Title:

Senior Manager, Clinical Data Standards

Company:

Ipsen Innovation (SAS)

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 company’s success. Join us on our journey towards sustainable growth, creating real impact on patients and society!

For more information, visit us at https://www.ipsen.com/ and follow our latest news on LinkedIn and Instagram.

Job Description:

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 reference 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 8–10 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 years of experience in a leadership role.
• Good level of expertise in the use of the data management and statistic software.
• Familiarity with define.xml, 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).

Nous nous engageons à créer un lieu de travail où chacun se sent écouté, valorisé et soutenu, où nous incarnons « The Real Us* ». La valeur que nous accordons aux différentes perspectives et expériences motive notre engagement en faveur de l'inclusion et de l'égalité des chances. Lorsque nous intégrons des modes de pensée diversifiés, nous prenons des décisions plus réfléchies et découvrons des solutions plus innovantes. Ensemble, nous nous efforçons de mieux comprendre les communautés que nous servons. Cela signifie que nous voulons également vous aider à donner le meilleur de vous-même lorsque vous postulez à un poste chez nous. Si vous avez besoin d'aménagements ou d'aide pendant le processus de candidature, veuillez en informer l'équipe de recrutement. Ces informations seront traitées avec soin et n'auront aucune incidence sur le résultat de votre candidature. *Soyons nous-même