Real World Evidence – Waterloo, Belgium (F/M)

Alsinova; Waterloo; On-site; EUR 70,000 - 90,000; Full time

Benefits offered by this job

an experience accelerator

access to diverse projects for clients

tailored career path

continuous learning

Job summary

Alsinova is looking for Real World Evidence Consultants to join our consulting team for clients’ projects based in Belgium. You will work on various activities including supporting statistical programming in RWE, study design input, protocol review, and ensuring efficient production of statistical outputs.

Applicants should have 5+ years in SAS programming, 2+ years in RWE/epidemiology, and experience with large healthcare databases.

Qualifications

• 5+ years experience in SAS programming.
• 2+ years experience in Real World Evidence, Epidemiology, or Health Outcomes.
• 2+ years experience with large health care databases such as CPRD or IBM MarketScan.
• Advanced SAS programming to solve complex tasks.
• Good study design and epidemiological/statistical analysis experience.
• Knowledge of propensity score matching is a plus.
• Knowledge of R is a plus.

Responsibilities

• 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.

Skills

SAS programming

Advanced SAS programming

Tools

R

Job description

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.

• Good written and verbal communication skills.
• Experience in communicating with alllevels of personnel across various departments, in domestic and internationalenvironments.
• Demonstrated experience in participating in collaborative work teams at local and globallevels.
• Good project management skills including experience in managing multiple tasksconcurrently.
• Ability to work under pressure and without close supervision. .

You:

• 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, includingunderstanding of drug development, observational and epidemiological endpoints andassessments.
• Knowledge of matching algorithms such as propensity score matching is a plus.
• Knowledge of R is a plus.

• Good command of English, both verbal and written.

• Good written and verbal communication skills.
• Experience in communicating with alllevels of personnel across various departments, in domestic and internationalenvironments.
• Demonstrated experience in participating in collaborative work teams at local and globallevels.
• Good project management skills including experience in managing multiple tasksconcurrently.
• Ability to work under pressure and without close supervision. .

Alsinova – An Astek Company

Alsinova is setting new standards for CROs by integrating multidisciplinary expertise with advanced technology.

Alsinova 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.

Alsinova is the subsidiary of the Astek Group, a global player in engineering and technology consulting. 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 10 000 employees who are committed every day to promoting combination of digital technologies and complex systems engineering.

Join a Group rapidly developing in France and around the world, with a turnover of 730 M€ in 2025.

More on the Group on our websites https://alsinova.com and https://astek.net.

Astek is committed to the employment of people with disabilities.

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 #TopEmployer2026 certified HR practices

Let’s move forward.