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Clinical Trial Supplies Manager

CK Group- Science, Clinical and Technical
Posted 8 days ago, valid for 10 days
Location

Uxbridge, Greater London UB81QS, England

Salary

£28.76 per hour

Contract type

Full Time

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Sonic Summary

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  • CK Group is seeking a Clinical Trial Supplies Manager for a global pharmaceutical company on a 6-month contract basis.
  • The position offers a salary of up to £30.03 per hour PAYE.
  • Candidates should have a degree in a relevant scientific subject or equivalent working experience, along with previous experience in the pharmaceutical industry.
  • Experience in a role focused on Clinical Supplies/Development with global exposure is required, along with strong knowledge of the global drug development process and regulatory requirements.
  • The role is remote but requires travel to the Uxbridge office 1-2 times a month.
CK Group are recruiting for a Clinical Trial Supplies Manager, to join a global pharmaceutical company, on a contract basis, for 6 months initially.

Salary:

Up to 30.03 per hour PAYE.

Clinical Trial Supplies Manager Role:
  • Collaborates with internal Global Clinical Supply Chain (GCSC) teams, external Customers & Service Providers Medical to ensure all needs are met.
  • Defines, plans, & communicates the clinical supply chain strategy in support of global clinical studies to promote optimal use.
  • Demonstrates strong knowledge of GCSC processes when presenting at cross-functional meetings.
  • Responsible for identifying and supporting strategies for continuous improvement.
  • Influences clinical and development timelines, study design & country selection.
  • Reviewing & providing input to draft clinical protocols, communicating timelines & investigational product strategies.

Your Background:
  • Degree in a relevant scientific subject or have equivalent working experience.
  • Previous working experience in the pharmaceutical industry.
  • Prior experience in a role focussed on Clinical Supplies/Development with global experience or equivalent experience.
  • Strong knowledge of the global drug development process & global regulatory requirements.
  • Strong knowledge of IVRS and CTMS systems.
Company:

Our client is the global leader in enabling pharma, biotech, and consumer health partners to optimize product development, launch, and full life-cycle supply for patients around the world. They have the goal of putting patients first and to help people around the world live better and healthier lives.

Location:

This role is remote with travel to the Uxbridge office 1-2 times a month.


Apply:

It is essential that applicants hold entitlement to work in the UK. Please quote job reference (Apply online only) in all correspondence.


Please note:

This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.

INDKA

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