Risk Management Lead

Job content

Make your mark for patients.

We’re here because we want to build the future and transform patients’ lives for the better.

At UCB, our people are our experiences and achievements, our passion and drive. That’s why we’re looking for talented individuals with diverse backgrounds and experiences - not just the best and brightest, but those who care about making a meaningful difference in the lives of patients. We promote an environment of diversity, openness, and respect where people can make valuable contributions.

An exciting journey lies ahead. Will you join us in pushing the boundaries of what’s possible?

Do you want to contribute to shaping the future of clinical trial oversight?

Join the Clinical Data and Innovation team as Risk Management Lead!

In recent years, a vast increase of study related Risk Management activities can be observed in the pharmaceutical industry, building a new foundation for study risk management and oversight. Here at UCB, we have accompanied the change in paradigm by implementing a Risk Management group starting as RBM in 2015 and has expanded to cover wider risk management activities. In these times of continuous changes, it is exciting to be part of a team contributing to shaping the future of clinical trial management.

The Risk Management team is seeking candidates foran additional position of (Associate) Risk Management Lead (RML). The RML works independently as an SME for Risk Based Approaches in the clinical trials, but at the same time is part of a global, highly collaborative Risk Management & Data Quality team within Clinical Data & Innovation Department. In this multifaceted role, driving the development and implementation for clinical study related risk assessment, management and oversight processes.

Working as an (Associate) RML you will focus to:

• Drive the development of study risk assessments and integrated quality risk management plans
• Guide and oversee the implementation of risk mitigations
• Perform protocol complexity assessments, reporting and trending
• Cooperate with many different stakeholders within UCB, including Clinical Project Management, Global Clinical Development, Statistical Sciences & Innovation, Clinical Development Quality, Patient Safety, Clinical Trial Supply, Global Medical Writing, IT, etc.
• Oversee contract research organization study risk management activities
• Detect and communicate emerging systematic study risks to appropriate company stakeholders
• Be a change agent within our organization, to help embed risk-based approaches for clinical studies

If you would like to know more about the RML role, please feel free to reach out to the Head of Risk Management & Data Quality, Joanna Florek-Marwitz, or one of Risk Management Leads in this group, John Daly or Norbert Dank.

We are happy to answer your questions!

About us.

UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are around 7,600 people in all four corners of the globe, inspired by patients and driven by science.

At UCB, everything we do start with a simple question: “How will this create value for people living with severe disease?”. We are on a journey to become the patient-preferred biopharma leader by delivering medicines and solutions that improve lives. We want to ensure the creation of patient value, now and into the future, while contributing to a society where a population of 8 billion people and more should be able to live a good life within limited resources of one planet.

Curious to know more? Please visit our website www.ucb.com.

UCB and its subsidiaries encourage diversity and inclusion in the workplace; we are an Equal Opportunity Employer. We do not discriminate on the basis of race/color/religion/sex/national origin/veteran/disability/age/sexual orientation/gender identity.