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Make your mark for patients
Are you passionate about advancing patient safety and drug development? Join our Brussels office in Belgium or Slough office in the UK.
About the Role
You will be working in a team that leads the strategic planning, delivery, and communication of benefit-risk assessments and risk management strategies for our medicines. Your focus will be on supporting clinical development from a safety perspective, identifying and assessing emerging safety concerns, evaluating benefit-risk outcomes, and supporting the implementation of risk management strategies that improve patient outcomes globally.
Who You’ll Work With
You will be collaborating in a diverse, cross-functional team, including experts in clinical development, regulatory affairs, patient engagement, medical affairs, and other stakeholders across the organization. The team values open communication, shared decision-making, and a commitment to patient safety.
What You’ll Do
* Analyze and interpret data from multiple sources to identify and assess potential new risks for assigned medicines.
* Incorporate new data into benefit-risk assessment plans.
* Implement safety monitoring and risk management strategies within clinical development programs.
* Identify areas requiring evidence generation, such as patient insights or real-world data, to support benefit-risk assessment plans.
* Serve as project manager, author, and reviewer of documents for regulatory submissions, ensuring clarity and compliance.
* Collaborate with internal teams to deliver high-quality and timely benefit-risk activities and outputs.
Qualifications
* Physician’s degree required (MD).
* Experience in pharmacovigilance, safety writing and benefit-risk planning. Experience in clinical development and regulatory submissions is an asset.
* Strong project management skills and ability to oversee multiple outputs and deadlines.
* Excellent communication and stakeholder engagement skills, both written and verbal, with the ability to present complex information clearly.
* Demonstrated ability to work collaboratively in cross-functional teams and with external stakeholders.
* Commitment to ethical decision-making and dedication to patient safety.
If you’re ready to make a meaningful impact on patient lives and contribute to patient safety, we invite you to apply and join our team!
About Us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9,000 people in all four corners of the globe, inspired by patients and driven by science.
Why work with UCB?
We don’t just complete tasks, we create value. We aren’t afraid to push forward, collaborate, and innovate to make our mark for patients. We have a caring, supportive culture where everyone feels included, respected, and has equal opportunities to do their best work.
UCB is an equal opportunity employer. All employment decisions will be made without regard to any characteristic protected by applicable laws.
Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on EMEA-Reasonable_Accommodation@ucb.com. Please note if your enquiry does not relate to adjustments; we will not be able to support you through this channel.
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