Head of Global Safety Data Integration and Literature

vor 4 Wochen

Monheim, Deutschland UCB Vollzeit

 

Make your mark for patients


Position: Head, Global Safety Data Integration and Literature

 

Make your mark for patients:

We are seeking an innovative, strong communicator and influencing Head, Global Safety Data Integration and Literature to join our leadership team in the Product Pharmacovigilance & Device Safety team, ideally based in our Raleigh (US), Monheim (Germany), Slough (UK) or Brussels (Belgium) offices.

 

About the role:

You will play a pivotal role in oversight and implementation of new and improved solutions to develop best in class safety business processes for standardized data collection in line with patient safety strategic objectives.  You will act at the primary point of contact within UCB for any regulatory queries and interactions with health authorities and lead Mission Regulatory discussions internally as part of the Patient Value Unit.

 

Who youâll work with

Reporting to the Head of Global Safety Reporting Operations, this position consolidates global and affiliate safety data integration owning the intake and literature screening process for UCBâs full product portfolio, including drugs, biologics, and combination products across all geographies.  This is a pivotal position in an evolving regulatory and technology focused environment that requires the ability to work with international and cross-functional teams, and the ability to interact with regulators during inspections and audits.

 

What youâll do:

  • Lead the execution of a comprehensive strategy for efficiently collecting safety information from multiple potential sources, including spontaneous reports, clinical studies, market research, social media, literature, and license partners.
  • Stay updated on the latest trends and emerging developments in safety data collection. Utilize this knowledge to drive continual improvements in processes leveraging technology, aligned with Patient Safety's automation objectives.
  • Ensure that collection methodologies facilitate timely, complete, and high-quality data, streamlining efficient case processing operations.
  • As the business process owner, drive the implementation of technology solutions to enhance data collection efficiency, supporting streamlined ICSR intake and literature operations while maintaining data accuracy and compliance.
  • Coordinate and lead a project team with affiliate teams to advocate for harmonization of intake processes, improving standardized procedures with vendors wherever possible, fostering consistency.
  • Serve as deputy delegate to Global Safety Reporting Operations Head and account for oversight of literature screening and management activities.
  • Provide oversight of advanced analytics and reporting capabilities to develop volume forecasting projections, identify trends, and potential risks.

 

Interested? For this position youâll need the following education, experience, and skills:

  • Bachelorsâ degree in health sciences, business or related field is required and masterâs degree preferred.
  • At least 5 years in the pharmaceutical industry in leadership roles relevant to pharmacovigilance.
  • Well defined experience with safety databases and case processing activities.
  • Demonstrated experience leading teams within the pharmaceutical industry, preferably in product pharmacovigilance & device safety teams.
  • Versed in serving as a lead in ICSR and Literature vendor management for governance oversight, optimizing vendor relationships, workload analysis and strategic capacity modelling.

 

If you are interested to learn more about R&D within UCB, please find more information here R&D at UCB.

 

RANDATUCB


Are you ready to âgo beyondâ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you 

About us 
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are around 8,500 people in all four corners of the globe, inspired by patients and driven by science. 

Why work with us? 
At UCB, we donât just complete tasks, we create value. We arenât 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 equitable opportunities to do their best work. We âgo beyondâ to create value for our patients, and always with a human focus, whether thatâs on our patients, our employees, or our planet. Working for us, you will discover a place where you can grow, and have the freedom to carve your own career path to achieve your full potential. 

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.
 
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 should your enquiry not relate to adjustments; we will not be able to support you through this channel.

 

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