Clinical Trial Supplies Manager

CK Group; Greater London; Remote; GBP 80,000 - 100,000; Full time

Job summary

A global pharmaceutical leader is seeking a Clinical Trial Supplies Manager for a 6-month contract. This home-based role involves collaboration with global teams to manage clinical supplies for studies. Candidates should have strong experience in clinical supplies and knowledge of the global drug development process. A key responsibility includes ensuring timely delivery of clinical supplies. Competitive hourly rate offered.

Qualifications

• Previous working experience in Clinical Supplies.
• Strong knowledge of related areas, including Manufacturing, Packaging & Labelling.
• Ability to translate broad strategies into specific objectives.

Responsibilities

• Collaborate with internal and external teams.
• Define, plan, and communicate clinical supply chain strategy.
• Ensure timely delivery of quality clinical supplies.

Skills

Clinical Supplies experience

Knowledge of global drug development process

Forecasting and Planning

Proficient in import/export requirements

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.

Salary: £28.76 ph. This role is inside IR35.

Clinical Trial Supplies Manager Role:

• Collaborate with internal Global Clinical Supply Chain (GCSC) teams and external Customers and Service Providers
• Proactively defines, plans, and communicates the clinical supply chain strategy in support of global clinical studies
• Responsible for identifying and supporting strategies for continuous improvement
• Ensures timely delivery of quality clinical supplies for all assigned compounds and protocols
• Participates in the development, review and approval of Interactive Response Technology (IRT) specifications. Develops investigation product distribution strategies and maintains distribution and supply strategies at depot and site level according to study

Your Background:

• Previous working experience in Clinical Supplies
• Knowledge of global drug development process and global regulatory requirements.
• Strong knowledge of Forecasting and Planning and proficient knowledge of related areas, i.e. Manufacturing, Packaging & Labelling, IVRS, Logistics, Quality, Stability, etc.
• Proficient knowledge of import/export requirements.
• Ability to translate broad strategies into specific objectives and action plans.

Our client is the global leader in enabling pharma, biotech, and consumer health partners to optimise 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 home-based, with one or two trips to Uxbridge per month.

To apply, please contact the Key Accounts Team on 01438 870011 or email [e-mail]. Please quote reference 156 466. It is essential that applicants hold entitlement to work in the UK. This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.