Real-World Evidence (RWE) Senior data scientist

h3Your mission /h3pWe are looking for an experienced, analytically strong, and versatile bRWE Senior Data Scientist /b to join our growing team. This role combines advanced statistical expertise and scientific research with project management and client-oriented consulting. You will play a key role in the design, execution, and interpretation of real-world evidence (RWE) projects. Working with data from medical registries and other real-world data sources, you will develop appropriate statistical approaches and translate complex results into scientifically robust and actionable insights. You will collaborate closely with physicians, scientific experts, medical registries, and leading pharmaceutical companies. In addition to providing scientific and methodological expertise, you will take responsibility for managing complex projects involving multiple stakeholders and contribute to developing new projects and client relationships. /ph3Your Responsibilities /h3ulliStudy design and planning: Develop suitable study designs, Statistical Analysis Plans (SAPs), and analytical strategies for a range of research questions and disease areas. /liliInterpretation and evidence generation: Independently interpret results and derive meaningful insights to inform clinical, scientific, and regulatory decision-making. /liliScientific publications: Contribute to and lead the preparation of scientific manuscripts, abstracts, and conference presentations, from interpreting results through to publication. /liliProject management: Plan, coordinate, and manage multiple projects involving diverse stakeholders, including pharmaceutical companies, medical registries, and clinical experts. /liliClient consulting and business development: Develop project concepts, prepare proposals and presentations, and pitch project ideas to prospective and existing clients. /liliStakeholder management: Build and maintain strong working relationships with clients, team members, healthcare professionals, data partners, and other project stakeholders. /liliMentoring and team development: Actively involve junior colleagues in projects, share knowledge, provide guidance and constructive feedback, and create opportunities for them to develop their skills, take ownership, and grow professionally. /liliContinuous improvement: Help advance our scientific methods, consulting services, and internal processes, while contributing to the professional development of the team. /li /ulh3Your profile /h3h3Required /h3ulliAcademic background: A Master's degree in a quantitative or scientific discipline, such as statistics, data science, epidemiology, pharmacoepidemiology, biostatistics, medicine, or a related field. A PhD is an advantage. /liliProfessional experience: Several years of relevant professional experience in statistical analysis, epidemiological research, medical evidence generation, or a related field. /liliHands-on methodological expertise: Demonstrated practical experience applying statistical methods. Experience with epidemiological research questions and appropriate methods for observational data is particularly important. /liliR programming: Hands-on experience programming in R within the last five years, with the ability to independently implement statistical analyses in a transparent and reproducible manner. /liliScientific publications: Experience contributing to scientific publications, for example through authorships of peer-reviewed articles. /liliProject management: Experience planning and managing projects involving multiple stakeholders and coordinating different professional perspectives. /liliLanguage skills: Excellent written and spoken German and English. /liliWorking style: Independent, structured, solution-oriented, and quality-conscious, with a high degree of ownership, flexibility, and accountability. /li /ulh3Nice to Have /h3ulliA PhD in a relevant field, such as epidemiology, pharmacoepidemiology, biostatistics, or a related quantitative discipline. /liliExperience in the pharmaceutical industry, particularly in real-world evidence research or regulatory environments. /liliKnowledge of advanced statistical methods, such as causal inference, propensity score methods, or longitudinal data analysis. /liliExperience working with medical registries, routine healthcare data, or other real-world data sources. /liliExperience preparing scientific conference contributions and presenting research findings to scientific and non-scientific audiences. /liliExperience consulting for pharmaceutical companies or other stakeholders in the healthcare sector. /li /ulh3Why us? /h3ulliUnique data access: Work with exclusive real-world datasets and medical registries (e.g. Neurology, Rheumatology, Gastroenterology, Dermatology) across multiple European countries. /liliScience meets consulting: Combine advanced statistical and epidemiological analyses with strategic thinking and client-oriented consulting. /liliHigh-impact projects: Collaborate with leading international pharmaceutical companies on scientifically and strategically relevant evidence generation projects. /liliRoom to shape your work: Take ownership of projects, contribute your own ideas, and actively shape study designs, client engagements, and our service portfolio. /liliEntrepreneurial culture: Benefit from flat hierarchies, fast decision-making, and direct interaction with clients, medical experts, and company leadership. /liliFlexibility and trust: Work predominantly remotely and organize your work with a high degree of autonomy and responsibility. For in-person collaboration, we typically meet one to two days per week at the Digital Health Center (DHC) coworking space in Bülach, Switzerland. /liliInnovation-driven environment: Use real-world evidence to support evidence-based healthcare decisions and advance the development of innovative digital health solutions. /li /ulh3About Us /h3pAt Rewoso, we specialize in the generation of high-quality real-world evidence to support clinical, regulatory, and strategic decision-making in healthcare. On a day-to-day basis, we work with real-world data from European medical registries—to design develop statistical approaches, and translate data into actionable insights in close collaboration with physicians and pharmaceutical partners. Building on this experience, we go beyond evidence generation: we leverage our deep understanding of real-world clinical practice and data to develop innovative digital health solutions that aim to improve patient outcomes. Learn more at: /p #J-18808-Ljbffr