Rwe Project Lead H/F - 75

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 705 M€ in 2024.More on the Group on our websites https://alsinova.com and https://astek.net.Astek is committed to the employment of people with disabilities.

Joining Astek means choosing:an experience accelerator, where every assignment is an opportunity to progressaccess to a multitude of technically exciting projects for our clients as well as internallyindividualized, local support for a tailored career pathcontinuous learning, thanks to our internal training academya friendly and inclusive work environment, supported by #TopEmployer2025 certified HR practicesLet's move forward.Alsinova, the Astek Group subsidiary offering a complete CRO solution, is recruiting a Senior Preclinical Biostatistician for a project in the pharmaceutical sector.
Your mission (should you decide to accept it):

As part of a strategic collaboration with leading healthcare companies, we are looking for experienced professionals in Real-World Evidence (RWE) to take on responsibilities as RWE Project Lead / Evidence Lead / Pharmacoepidemiologist.

You will play a key role in the design, coordination, and delivery of RWE studies, ensuring scientific excellence and compliance with regulatory standards.

Your daily activities will be:

- Lead and coordinate RWE projects end-to-end, from study design to delivery.
- Define methodological approaches and ensure scientific robustness of analyses.
- Collaborate with cross-functional teams (epidemiology, biostatistics, data science, market access, clinical).
- Manage interactions with internal stakeholders and external partners (CROs, academic institutions, regulatory bodies).
- Provide expert advice on pharmacoepidemiology, study feasibility, data sources, and methodologies.
- Contribute to the development of best practices, standards, and guidance for RWE activities.