Manager Statistical Programming for SDTM (m/f/x)

Passion for Innovation. Compassion for Patients.

With over 120 years of experience and more than 17,000 employees in over 20 countries, Daiichi Sankyo is dedicated to discovering, developing, and delivering new standards of care that enrich the quality of life around the world.

In Europe, we focus on two areas: The goal of our Specialty Business is to protect people from cardiovascular disease, the leading cause of death in Europe, and help patients who suffer from it to enjoy every precious moment of life. In Oncology, we strive to become a global pharma innovator with competitive advantage, creating novel therapies for people with cancer.

Our European headquarters are in Munich, Germany, and we have affiliates in 13 European countries and Canada.

For our headquarters in Munich we are seeking highly qualified candidates to fill the position:

Manager Statistical Programming for SDTM (m/f/x)

The Position:

The purpose of this job is to participate in development or validation or provide vendor oversight for statistical vendor deliverables, perform programmatic generation or review of aCRF, SDTM specification, SDTM datasets, SDRG and define package, ensure deliverable quality, and expedite the preparation of oncology compound regulatory submission. It is also expected to maintain institutional knowledge across oncology compounds and support building up oncology programming standard to improve efficiency and quality.

Roles & Responsibilities:

• By leading internal programming contractor or by self, perform programmatic generation of statistical deliverables, ensure deliverable quality for the pivotal studies, Integrated Summary of Efficacy (ISE)/ Integrated Summary of Safety (ISS) for oncology submission compounds, and expedite the preparation of regulatory submissions. Responsibilities include: generate or review Case Report Form (CRF) annotation and Study Date Tabulation Model (SDTM) dataset, identify data inconsistencies and support data review, ensure dataset in compliance with CDISC and submission requirement, generate or review submission data package and ensure its quality and integrity
• Oversee statistical programming vendor on project planning and execution to ensure high quality deliverables and timelines met. Responsibilities include: review and agree on vendor project timelines and resource planning, work in tandem with Biostatistics and Data Management members to ensure best vendor performance, monitor statistical deliverable transfers for ongoing and complete trials, confirm data use and output quality, proactively ensure the resolution of programming related issues prior to database lock analysis, be accountable and verify completeness of study programming deliverables, maintain all required study programming documentation required for Trial Master File (TMF).
• Maintain institutional knowledge across oncology compounds and support building up oncology programming standard on datasets and TFLs to improve efficiency and quality. Responsibilities include: contribute to CRF and SDTM standard development, support develop, implement, and maintain Analysis Data Model (ADaM) dataset and TLF standard, develop sample programs to generate standard ADaM dataset and TLFs, support training and ensure implementation of ADaM and TLFs standard in clinical trials analysis
• Provide programming support to prepare regulatory requested analyses and help submission team in quick turnaround in response to regulatory agencies. Responsibilities include: create TLFs to support submission Q&As in a quick turnaround, support ad-hoc and exploratory analysis requested by clinical team, provide programming supports in agency response or potential Advisory Committee Meeting
• Develop and maintain programming macros to effectively support internal data review and monitoring. Responsibilities include: work with Biostatistics member to define the requirements of efficacy data review, develop macros and support the internal data review and monitoring on an ongoing basis

Education & Professional Experience:

• Bachelor’s degree with minimum 7 years proven experience within pharmaceutical industry, or CROs supporting statistical analysis of clinical trials programming
• Advanced working knowledge of all aspects of the SAS programming language used in clinical trials programming
• Advanced working knowledge of CDISC SDTM and ADaM, and extensive experiences of their implementation in clinical trials analysis
• Advanced understanding of statistical concepts in support of analyses and reporting of clinical trials
• Having knowledge of all phases of drug development, including early and late phase clinical development and submission
• Having solid background of applied statistics
• Solid knowledge of new advanced statistical methods using SAS and R
• Knowlede in database structures and set-up
• The candidate should have successfully provided programming expertise at the Project level for at least two global development projects that have been submitted to regulatory agencies
• Strong project management skills
• Strong organizational skills, problem-solving abilities, time management skills and initiative
• Flexibility and ability to work on several assignments simultaneously. Must be able to work independently as well as part of a team
• Superior written and oral communications skills in the English language

Why work with us?

Working at Daiichi Sankyo is more than just a job – it is your chance to make a difference and change patients’ lives for the better. We can only achieve this ambitious goal together. That is why we foster a culture of mutual respect and continuous learning, with a strong commitment to inclusion and diversity. Here, you will have the opportunity to grow, think boldly, and contribute your ideas. If you have a proactive mindset and passion for addressing the needs of patients, we eagerly await your application.

For more information: www.daiichi-sankyo.eu