Debiopharm

Biopharmaceutical

SeniorManager,StatisticalProgramming

Lausanne, Switzerland FULL TIME Remote Friendly
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Senior candidates.

The Brief

“Senior Manager, Statistical Programming at Debiopharm. Skills: Statistical Programming, AI adoption, Digitalization strategy, Team leadership. Provide strategic leadership for Statistical and Clinical Data Science Programming. Implement cutting-edge data science technology and AI adoption”

What You'll Achieve.

Improving the lives of people affected by cancer and infectious diseases; Streamline clinical data processing and analysis; Ensure the highest quality of deliverables for our clinical projects; Ensure efficient, integrated project reporting and adherence to standards; Ensure all activities strictly adhere to GCP, SOPs, and regulatory requirements for electronic data submissions

Industry & Context.

Biopharmaceutical

What They're Looking For.

Must Have

MSc in Statistics, Biostatistics, Mathematics, Computer Science, or equivalent experience, At least 7 years of statistical programming experience within pharmaceutical clinical development, Extensive knowledge of SAS software and general computing techniques, Thorough understanding of clinical trial design, reporting processes, and software development/validation methodologies

What You'll Do.

Provide strategic leadership for Statistical and Clinical Data Science Programming

Implement cutting-edge data science technology and AI adoption

Streamline clinical data processing and analysis

Lead a team of programmers and data scientists

Ensure the highest quality of deliverables for clinical projects

Manage a team of statistical programmers

overseeing resource planning

and professional development

Lead the roadmap for AI adoption and new technical solutions for integrating and reporting clinical data

Accountable for the quality and timelines of all programming deliverables (datasets

TLFs) for study reports and integrated summaries

Provide technical guidance to CRO partners

Ensure all activities strictly adhere to GCP

and regulatory requirements for electronic data submissions

How You'll Work.

Team & Collaboration

Partner closely with Biostatistics, Data Management, IT, and Clinical Development functions; Maintain successful cross-functional partnerships

Communication Scope

Proactive communicator

Process & Methodology

Resource planning, Talent acquisition

Full Job Description

### _**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, we’re 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 activit

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