Biostatistician & SAS Programmer

pAt Terumo, we advance lifesaving medical technologies to benefit society. Are you eager to make a difference with us? Here, you’ll grow your expertise while staying true to your personal aspirations. /ppGuided by our Japanese heritage, we act with respect, take ownership, and pursue continuous improvement. If you see yourself in our values, keep reading; this might be the opportunity you're looking for. /ph3bDepartment Info /b /h3pThe Biometrics team within Terumo's EMEA Clinical Medical (CM) organization is a close-knit team,bringing together biostatistics, SAS programming and Clinical Data Management expertise. The team partners closely with Clinical and Medical Affairs colleagues to generate high-quality clinical evidence supporting our medical devices, from study set-up and data collection through analysis and dissemination of results. /ph3bJob Summary /b /h3pAs our bBiostatistician SAS Programmer /b, you will take statistical ownership of clinical studies, from study design and sample-size calculations to statistical analysis, interpretation and communication of results. You will combine strong biostatistical expertise withhands-on SAS programming, working closely with ourprogrammers, Data Management andClinical and Medical Affairs colleagues. /ppAt the same time, you'll help shape how Biometrics evolves by bringing new ideas around statistical methodology, automation, analytics and the opportunities created by AI. /ph3bJob Responsibilities /b /h3ulliAct aslead biostatistician for assigned clinical studies, taking statistical ownership from study design through analysis, interpretation and dissemination. /liliProvide statistical input into study design, endpoints, sample-size calculations, randomization and Clinical Investigation Plans/protocols. /liliDevelop, review and approve Statistical Analysis Plans (SAPs), TFL specifications and related statistical documentation. /liliStay hands-on with SAS: develop, optimize and automate programs, analysis datasets and statistical outputs, and develop or debug SAS macros where required. /liliWork closely with SAS programmers, fellow biostatisticianand Clinical Data Management colleagues, coordinating and reviewing programming activities where appropriate. /liliPartner with Medical Affairs and Clinical colleagues to understand their questions, select appropriate statistical approaches and translate analyses into clear, meaningful conclusions. /liliCritically assess study results, clearly explaining what the data supports, what it does not support and what conclusions can be drawn. /liliContribute statistical expertise to data-management activities, including CRF/FRS review, UAT, data-review activities and endpoint-related edit checks. /liliEnsure statistical deliverables meet scientific, regulatory and quality requirements and maintain appropriate traceability across the data lifecycle. /liliHelp shape the future of Biometrics by contributing to standardization and automation and exploring new analytical, visualization and AI-driven approaches that improve quality and efficiency. /li /ulh3bProfile Description /b /h3pDegree inBiostatistics, Statistics, Mathematics or a closely related quantitative discipline. /ppAt least 4 years of relevant experience in biostatistics and clinical research, ideally within a medical device, CRO, pharmaceutical or biotech environment. /ppStrong, hands-on SAS expertise is essential, including the ability and willingness to program independently. /ppSolid experience across clinical study statistics, including study design, sample-size calculations, SAPs, statistical analyses and interpretation of results. /ppExperience working across multiple studies, clients or changing priorities is particularly valuable. /ppKnowledge of R and/or Python is an advantage; exposure to Power BI is a plus. /ppStrong communication skills, with the ability to translate complex statistical concepts and results into clear messages for non-statistical stakeholders. /ppA collaborative, approachable and solution-oriented mindset, combined with the confidence to challenge constructively, listen to different perspectives and work towards practical solutions. /ppA strong quality and process mindset, balanced with the pragmatism, adaptability and ownership needed in a fast-moving medical device environment. /ppFluency in English, confidence working in an international and multicultural environment, and willingness to travel occasionally within Europe and potentially beyond. /ph3bOffer /b /h3pIn this role, you'll have the opportunity to take real ownership of your studies while having the autonomy to organize your work and deliverables. At the same time, you'll be part of a collaborative Biometrics team where colleagues exchange ideas, discuss statistical methods and support each other across studies. /ppYou'll work closely with Clinical, Medical Affairs, Data Management and SAS Programming colleagues, giving you the opportunity to contribute throughout the stud