Real World Evidence - Waterloo, Belgium (F/M) | Alsinova · Teeming.ai
Alsinova
Alsinova provides end-to-end life science research services that combine medical expertise with AI-driven tools. As a non-clinical and clinical research company, Alsinova uses a Digital CRO approach,…
BioEquivalenceBiostatisticsClinical Data FabricClinical OperationsClinical Project ManagementClinical ResearchConsultingData ManagementData SciencesDecentralized Clinical TrialsDigital EnablementeHealthFSPLife SciencesMedical WritingPhase I to IVQuality AssuranceRegulatoryRWESafetyVigilancealsinova.com
Alsinova
Alsinova provides end-to-end life science research services that combine medical expertise with AI-driven tools. As a non-clinical and clinical research company, Alsinova uses a Digital CRO approach,…
BioEquivalenceBiostatisticsClinical Data FabricClinical OperationsClinical Project ManagementClinical ResearchConsultingData ManagementData SciencesDecentralized Clinical TrialsDigital EnablementeHealthFSPLife SciencesMedical WritingPhase I to IVQuality AssuranceRegulatoryRWESafetyVigilancealsinova.com
HQBoulogne-Billancourt, FR
Team Size216
Open Jobs26
Total Funding-
Latest FundraiseUnknown
Join the Team
Real World Evidence - Waterloo, Belgium (F/M)
HybridWaterloo, Walloon Region, BE
Hybrid • Waterloo, Walloon Region, BE
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What we will accomplish together:
Alsinova is looking on
a regular basis for Real World Evidence Consultants
to join our consulting team for clients' projects (from big pharma to small biotech) based in
Belgium.Your mission (should you decide to accept it):
Your potential challenges will be various, depending on the clients' priorities. The list below gives you examples of our classic activities.
Your daily activities will be:
Support Statistical programming activities in Real World Evidence.
Provide input on study design and analysis plans where necessary.
Review the study concept, protocol design, analysis plans and other study-related documents.
Evaluate the quality of the database.
Develop, validate, maintain, and document analysis programs, tables, charts and associated metadata following standard working practices.
Ensure that statistical outputs are produced in an efficient manner.
You:
Our Benefits
Joining Astek means choosing:
an experience accelerator, where every assignment is an opportunity to progress
access to a multitude of technically exciting projects for our clients as well as internally
individualized, local support for a tailored career path
continuous learning, thanks to our internal training academy
a friendly and inclusive work environment, supported by #TopEmployer2025 certified HR practices Let's move forward.
5+ years experience in SAS programming.
2+ years experience in Real World Evidence, Epidemiology, or Health Outcomes environment.
2+ years experience with large health care databases such as Clinical Practice Research Database (CPRD) or IBM MarketScan.
Advanced statistical programming skills in SAS to solve complex programming tasks.
Good study design and epidemiological/statistical analysis experience, including understanding of drug development, observational and epidemiological endpoints and assessments.
Knowledge of matching algorithms such as propensity score matching is a plus.
Knowledge of R is a plus.
Good written and verbal communication skills.
Experience in communicating with all levels of personnel across various departments, in domestic and international environments.
Demonstrated experience in participating in collaborative work teams at local and global levels.
Good project management skills including experience in managing multiple tasks concurrently.
Ability to work under pressure and without close supervision. .
