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(senior) benefit risk scientist

Braine-l'Alleud
Publiée le Publiée il y a 14 h
Description de l'offre

Make your mark for patients


We are looking for a (Senior) Benefit Risk Scientist who is analytical, collaborative, and detail-oriented to join us in our Patient Benefit Risk and Medical Safety team, based in our Braine l’Alleud office in Belgium.

About the role

You will contribute to the evaluation, interpretation, and communication of benefit–risk insights across several medicines at different stages of development. You will support the creation of safety and benefit–risk strategies, contribute to scientific documentation, and ensure high‑quality analyses aligned with regulatory requirements.

Who you’ll work with

You will be working in a team that collaborates closely with medical, clinical, statistical, and regulatory colleagues. You will partner with Benefit Risk Leads and cross-functional teams to monitor and communicate the benefit–risk profile of each medicine.

What you’ll do

• Analyse and interpret data from multiple sources to identify and assess potential new risks and incorporate findings into benefit–risk plans.

• Support the implementation of safety monitoring and risk management strategies in clinical development programs.

• Prepare and contribute to high‑quality benefit–risk and safety documentation for regulatory submissions.

• Ensure scientific accuracy, clarity, and compliance in all written deliverables.

• Collaborate with stakeholders to ensure timely escalation and alignment on safety topics.

• Stay current on scientific and regulatory developments relevant to benefit–risk assessment.

Interested? For this role we’re looking for the following education, experience and skills

• Bachelor’s degree in a scientific field (required); Master’s or advanced degree (desired).

• Experience in the biopharmaceutical industry with exposure to safety evaluation or benefit–risk assessment.

• Demonstrable experience in supporting multiple safety-related outputs and working knowledge of the international regulations governing drug safety.

• Ability to analyse complex data and communicate findings clearly.

• Strong organisational skills with the ability to work on multiple projects.

• Excellent written and verbal communication skills in English.

• Ability to adapt in dynamic environments and apply sound judgement.


Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

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