Clinical Project Manager Team Lead (UK)

at  UCB

Slough, England, United Kingdom -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate18 Jan, 2025Not Specified19 Oct, 2024N/AChange Management,Collaboration,Conflict,Clinical Research Associates,Facilitation,Groups,Project Managers,Teams,People Management,Analytical Skills,It,International EnvironmentNoNo
Add to Wishlist Apply All Jobs
Required Visa Status:
CitizenGC
US CitizenStudent Visa
H1BCPT
OPTH4 Spouse of H1B
GC Green Card
Employment Type:
Full TimePart Time
PermanentIndependent - 1099
Contract – W2C2H Independent
C2H W2Contract – Corp 2 Corp
Contract to Hire – Corp 2 Corp

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