Make your mark for patients

We are looking for a Clinical Project Manager Team Lead who is curious, analytical and collaborative to join us in our Patient Value Development Solutions/GCSO department, based in our office in Monheim (Germany), Slough (England) or Brussels (Belgium).


About the role
The Clinical Project Manager (CPM) Team Lead will lead and manage a team of Senior/Clinical Project Managers based in United States (US), European Union (EU) and Asia. The CPM Team Lead ensures that the CPM team deliver well-designed patient centric protocols, integrating industry-leading technology, producing high quality data within budget and timelines.


Who you’ll work with
Reporting to the Head Clinical Project Manager, you will manage a global established team of 6 – 10 Clinical Project Managers who share a collaborative work environment. As a Clinical Project Manager Team Lead, you will also be working closely with in our house Clinical Research Associate Team, Clinical Development Team, Asset Heads and Global Medical Affairs and external Clinical Research Organisations.


What you’ll do
Apart from what has been mentioned below:

• Management and Mentorship: Guide CPMs to ensure their personal and professional development while representing the team externally.
• Operational Support: Ensure effective planning and delivery of clinical studies throughout phase I – IIIb and NIS.
• Communication and Coordination: Act as a point of contact between internal teams and partners for study-related inquiries.
• Ensure compliance with timelines and budgets, identify risks, and develop mitigation plans.
• Process Improvement: Seek and initiate opportunities for improvement to enhance organizational effectiveness.
• Compliance and Credibility: Ensure regulatory Compliance and support Audits and Inspections

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

• Bachelor’s degree in a relevant scientific or healthcare related field and over 5 years of experience in the pharmaceutical, biotech, or CRO industry, with a proven track record in leading global clinical studies, preferably with leading Clinical Project Managers or Clinical Research Associates.
• Experience leading global, cross-functional teams, with strong people management, facilitation, and mentorship skills.
• Deep understanding of clinical trial processes, project management tools, and change management, with a results-oriented approach.
• Strong analytical skills, ability to synthesize information, and present it clearly to individuals and groups.
• Skilled in inspiring, persuading, and influencing others, with a strong customer orientation and collaboration across teams and departments.
• Innovative thinker who challenges the status quo, capable of solving complex problems and managing conflict, especially in a dynamic and international environment.

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 ‘go beyond’ 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 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 equitable opportunities to do their best work. We ‘go beyond’ to create value for our patients, and always with a human focus, whether that’s 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.