Real World Evidence Consultant

ppstrongWhat we will accomplish together: /strong /ppAlsinova is looking on stronga regular basis for Real World Evidence Consultants /strong to join our consulting team for clients’ projects (from big pharma to small biotech) based in strongBelgium. /strong /ppstrongYour mission (should you decide to accept it): /strong /ppYour potential challenges will be various, depending on the clients’ priorities. The list below gives you examples of our classic activities. /ppstrongYour daily activities will be: /strong /pulliSupport Statistical programming activities in Real World Evidence. /liliProvide input on study design and analysis plans where necessary. /liliReview the study concept, protocol design, analysis plans and other study-related documents. /liliEvaluate the quality of the database. /liliDevelop, validate, maintain, and document analysis programs, tables, charts and associated metadata following standard working practices. /liliEnsure that statistical outputs are produced in an efficient manner. /li /ulpstrongYou: /strong /pulli5+ years experience in SAS programming. /li /ululli2+ years experience in Real World Evidence, Epidemiology, or Health Outcomes environment. /lili2+ years experience with large health care databases such as Clinical Practice Research Database (CPRD) or IBM MarketScan. /liliAdvanced strongstatistical programming skills in SAS /strong to solve complex programming tasks. /liliGood strongstudy design and epidemiological/statistical analysis experience /strong, includingunderstanding of drug development, observational and epidemiological endpoints andassessments. /liliKnowledge of matching algorithms such as propensity score matching is a plus. /liliKnowledge of R is a plus. /li /ululliGood written and verbal communication skills. /liliExperience in communicating with alllevels of personnel across various departments, in domestic and internationalenvironments. /liliDemonstrated experience in participating in collaborative work teams at local and globallevels. /liliGood project management skills including experience in managing multiple tasksconcurrently. /liliAbility to work under pressure and without close supervision. . /li /ululliGood command of English, both verbal and written. /li /ulpAlsinova – An Astek Company /ppstrongAlsinova is setting new standards for CROs by integrating multidisciplinary expertise with advanced technology. /strongAlsinova offers a complete CRO solution, providing innovative, customised solutions in various life science segments: pharmaceuticals, biotechnology, medical devices, cosmetics, agri-food, veterinary and healthcare institutions. /ppAlsinova is the subsidiary of the Astek Group,strong a global player in engineering and technology consulting. /strong Since its creation, the Group has based its development on a strong culture of entrepreneurship and innovation, and on the support and skills development of its strong10 000 employees /strong who are committed every day to promoting combination of digital technologies and complex systems engineering. /ppstrongJoin a Group rapidly developing in France and around the world, with a turnover of 730 M€ in 2025. /strong /ppMore on the Group on our websites and /ppstrongAstek is committed to the employment of people with disabilities. /strong /ppstrongOur benefits /strong /ppJoining Astek means choosing: /pullian experience accelerator, where every assignment is an opportunity to progress /liliaccess to a multitude of technically exciting projects for our clients as well as internally /liliindividualized, local support for a tailored career path /lilicontinuous learning, thanks to our internal training academy /lilia friendly and inclusive work environment, supported by #TopEmployer2026 certified HR practices /li /ulpstrongLet’s move forward. /strong /p /p