Clinical Trial Supplies Manager
Posted 1 week ago by CK Group
£29 Per hour
Inside
Hybrid
United Kingdom
Summary: The Clinical Trial Supplies Manager will work with a global pharmaceutical company on a 6-month contract, focusing on the clinical supply chain strategy for global studies. The role involves collaboration with internal teams and external partners to ensure effective supply chain management and continuous improvement. The position requires strong knowledge of clinical supplies and drug development processes, along with the ability to influence study design and timelines. This is a remote role with occasional travel to the Uxbridge office.
Key Responsibilities:
- Collaborate with internal Global Clinical Supply Chain teams and external partners to meet clinical supply needs.
- Define, plan, and communicate the clinical supply chain strategy for global clinical studies.
- Demonstrate knowledge of GCSC processes in cross-functional meetings.
- Identify and support strategies for continuous improvement in clinical supplies.
- Influence clinical and development timelines, study design, and country selection.
- Review and provide input to draft clinical protocols and communicate timelines and investigational product strategies.
Key Skills:
- Degree in a relevant scientific subject or equivalent working experience.
- Previous experience in the pharmaceutical industry.
- Experience in a role focused on Clinical Supplies/Development with global experience.
- Strong knowledge of the global drug development process and regulatory requirements.
- Strong knowledge of IVRS and CTMS systems.
Salary (Rate): £28.76 per hour
City: Uxbridge
Country: United Kingdom
Working Arrangements: hybrid
IR35 Status: inside IR35
Seniority Level: Mid-Level
Industry: Other
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 £28.76 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 is a remote role 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 134 171 in all correspondence. Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.