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Clinical Trial Supplies Manager
Posted 7 hours 27 minutes ago by New Scientist
Permanent
Not Specified
Healthcare & Medical Jobs
Surrey, Epsom, United Kingdom, KT171
Job Description
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:
Your Background:
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 in all correspondence.
Please note:
This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.
INDKA
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.
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 in all correspondence.
Please note:
This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.
INDKA
New Scientist
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