Lead Statistical Programming Architect – Macro, Automation & AI

Ipsen; Paris; Sur place; EUR 70 000 - 100 000; Plein temps

Résumé du poste

Ipsen seeks a Lead Statistical Programming Architect based in Paris. This role is key in enhancing efficiency and quality in biometry through the automation of programming tasks, providing strategic guidance to programming teams. Candidates need strong experience in SAS programming and clinical trial processes along with the capability to lead technical initiatives. Proficiency in English is essential, with French being preferred. This position offers opportunities for influence across therapeutic areas including Oncology and Neurosciences.

Qualifications

• 5+ years of experience in statistical programming within a pharmaceutical/clinical trial environment.
• Strong understanding of regulatory requirements like CDISC and ICH.
• Experience with automation frameworks for clinical programming.

Responsabilités

• Develop technical solutions for statistical programming activities.
• Provide leadership and technical guidance to programming teams.
• Collaborate with cross-functional teams to enhance programming capabilities.

Connaissances

SAS programming language

Statistical programming

Clinical trial processes

Automation frameworks

Cloud computing

R programming

Formation

Bachelor's degree in computer science

Outils

SAS

R

Java

Python

Description du poste

WHAT - Summary & Purpose Of The Position

The Lead Statistical Programming Architect – Macro, Automation & AI role is responsible for making decisions and recommendations that impact efficiency, timeliness, and quality of deliverables from biometry. This role will provide leadership, direction and technical and project specific guidance to programming teams across therapeutic areas such as Oncology, Rare Disease, and Neurosciences.

The role acts as a strategic technical leader responsible for shaping the long-term vision of programming technologies, driving digital transformation within biometry, and influencing cross-functional data and analytics strategies across R&D.

The role partners closely with Data Management, Biostatistics, Clinical Development, IT, and external vendors to ensure that technical solutions support regulatory compliance, operational efficiency, and innovation in clinical data analysis and reporting.

WHAT - Main Responsibilities & Technical Competencies

• Develops and/or coordinates the development of technical solutions (e.g. SAS macros, SAS template programs for datasets and TFLs, R functions/packages and tools, ADaM specification template) that support the automation of clinical and/or statistical programming activities inside global biometry, providing technical support and training as needed.
• Provides technical guidance and collaborates with IT, QA, System, and external vendors to build/maintain a robust, controlled, and productive statistical computing environment.
• Develops and implements robust software development plans including user requirement specifications, functional specifications, design specifications, and test plans and scripts as required.
• Develops and/or coordinates technical tools to enhance quality control, traceability, and good documentation practices for biometric practices.
• Collaborates with the user community and internal/external collaborators to identify innovation, automation, and continuous process improvement opportunities.
• Serves as a departmental lead in areas of technical expertise. Coaches and trains clinical and/or statistical programmers to support the continuous improvement of technical capabilities.
• Connects with cross functional groups within global biometry to identify, influence and tap into connections in strategy, processes, standards and innovations across therapeutic areas.
• Maintains up to date industry knowledge of processes, trends and technologies ensuring efficient implementation and adoption to support current and future needs.
• Evaluates third‑party software application(s) targeted for possible integration into the overall solution, including strategic application(s), tools and utilities.
• Develops and builds application(s) libraries, global code repositories and automation tools to support global standards for Clinical and/or statistical programming.
• Demonstrable knowledge of SAS programming language including SAS/MACRO, SQL and SAS/BASE procedures, SAS/GRAPH and Statistical procedures.
• Demonstrable knowledge of regulatory requirements (FDA, ICH), such as CDISC, SDTM/ADaM IG etc.
• Defines and drives the global technical strategy for programming automation, standardization and advanced analytics capabilities within Global Biometry.
• Identifies and implements emerging technologies, modern programming frameworks and cloud‑based platforms to improve the efficiency, scalability and traceability of clinical programming activities.
• Ensures all technical solutions comply with regulatory expectations and internal quality standards.
• Demonstrable experience in organizing NDA/s NDA regulatory submissions;
• Demonstrable experience of Clinical data and medical dictionaries;
• Demonstrable understanding of clinical trials - how programming deliverables fit into the process, what types of data are collected, mapped, and analysed;
• Demonstrable experience working with developing tools and supporting cloud‑based platforms;
• Software design experience with other languages (e.g. R, Java C++, JavaScript, Python etc.) highly preferred.

HOW - Behavioural Competencies Required

• Cultivate innovation: creating new and better ways using latest technology advancements for the function to be successful.
• Adaptability: Adjusting to changes while maintaining high performance and necessary compliance.
• Drive engagement: creating a climate where people are motivated to contribute to standardization and process improvement
• Strategic mindset: Demonstrates the ability to translate long‑term business priorities into scalable technical solutions.
• Influence and collaboration: Builds strong relationships across functions and influences stakeholders without direct authority.
• Develops talent: Coaches and mentors programming staff to strengthen technical expertise and promote continuous improvement.
• Decision quality: Makes timely, well‑informed technical decisions balancing innovation, compliance and operational feasibility.

HOW - Knowledge & Experience

Knowledge & Experience (essential):

• Experience in statistical programming and software development and testing in a pharmaceutical/ clinical trial environment.
• Experience designing and implementing programming tools supporting clinical trial analysis and regulatory submissions.
• Strong understanding of clinical trial processes and regulatory requirements related to statistical programming.
• Extensive experience leading technical initiatives or platforms within global programming or biometry organizations.
• Demonstrated experience implementing automation frameworks or standards across multiple clinical programs.

Knowledge & Experience (preferred)

• Experience working within global matrix R&D organizations and collaborating with cross‑functional teams.
• Experience with modern analytics environments such as R‑based workflows, cloud computing environments or integrated data platforms.
• Experience contributing to industry standards development or professional working groups

Education / Certifications (essential)

• Bachelor’s degree or equivalent in computer science, mathematics, data science/analytics, public health or other relevant scientific field (or equivalent theoretical/technical depth).

Education / Certifications (preferred)

• Advanced Degree (Master’s, PhD or equivalent) preferred.

Language(s) (essential)

• English

Language(s) (preferred)

• French