P2612 Senior Manager Statistical Programming

Together we innovate we impact we grow !

At Debiopharm every step we take is guided by one purpose: improving the lives of people affected by cancer and infectious diseases. As a privately-owned Swiss biopharmaceutical company were driven by science but above all by the people behind every treatment the patients and their families.

Through our unique development only model we bring forward promising therapies and transform them into treatments that can reach those who need them most faster.

We are currently looking for a motivated and collaborative professional to join our Biostatistics and Data Management (R&D) Department based at our Headquarters in Lausanne Switzerland as

Senior Manager Statistical Programming

Permanent role Lausanne Switzerland

Your Mission:

As the Senior Manager of Statistical Programming you will provide strategic leadership for Statistical and Clinical Data Science Programming. You will be the driving force behind our digitalization strategy implementing cutting-edge data science technology and AI adoption to streamline clinical data processing and analysis. Beyond strategy you will lead a talented team of programmers and data scientists to ensure the highest quality of deliverables for our clinical projects.

Your Key Responsibilities

Leadership & Management: Manage a team of statistical programmers overseeing resource planning talent acquisition and professional development.

Strategic Digitalization: Lead the roadmap for AI adoption and new technical solutions for integrating and reporting clinical data.

Operational Excellence: Accountable for the quality and timelines of all programming deliverables (datasets TLFs) for study reports and integrated summaries.

Vendor Oversight: Provide technical guidance to CRO partners to ensure efficient integrated project reporting and adherence to standards.

Compliance: Ensure all activities strictly adhere to GCP SOPs and regulatory requirements for electronic data submissions.

Cross-Functional Collaboration: Partner closely with Biostatistics Data Management IT and Clinical Development functions.

Your Profile

Education: MSc in Statistics Biostatistics Mathematics Computer Science or equivalent experience.

Experience: At least 7 years of statistical programming experience within pharmaceutical clinical development.

Technical Expertise: Extensive knowledge of SAS software and general computing techniques.

Industry Knowledge: Thorough understanding of clinical trial design reporting processes and software development/validation methodologies.

Soft Skills: Proactive communicator with the ability to adapt quickly to changing organizational needs and maintain successful cross-functional partnerships.

What we Offer:

Being part of a company where innovation collaboration and impact arent just values theyre how we work every day

Partner with teams across disciplines at the forefront of oncology and anti-infective development

An inclusive and respectful workplace proud to be Equal-Pay certified

Grow in a culture that values people purpose and performance

A chance to grow share and shape the future of healthcare

What to Expect in the Recruitment Process:

If your application is selected youll be invited to interviews with Talent Acquisition and the Hiring Manager via Teams followed by a panel interview and reference checks. Communication is handled via Workablecheck your spam folder for emails from *@.

Please contact our HR Department prior to submitting any profiles. We cannot accept unsolicited applications from agencies or recruiters.

Required Experience:

Senior Manager