Clinical Project Manager Team Lead (UK)
at UCB
Slough, England, United Kingdom -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 18 Jan, 2025 | Not Specified | 19 Oct, 2024 | N/A | Change Management,Collaboration,Conflict,Clinical Research Associates,Facilitation,Groups,Project Managers,Teams,People Management,Analytical Skills,It,International Environment | No | No |
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Description:
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 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.
Responsibilities:
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.
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.
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
Leading global clinical studies preferably with leading clinical project managers or clinical research associates
Proficient
1
Slough, United Kingdom