At a Glance
- Tasks: Design and execute supply chains for global clinical studies, ensuring smooth operations.
- Company: Leading pharmaceutical company focused on innovative drug development.
- Benefits: Hybrid working, competitive salary, and opportunities for professional growth.
- Other info: Collaborative environment with a focus on innovation and career advancement.
- Why this job: Make a real impact in healthcare by optimising supply chains for clinical trials.
- Qualifications: Experience in supply chain management and strong stakeholder engagement skills.
The predicted salary is between 35000 - 45000 £ per year.
Role - Clinical Study Supply Lead Location - Macclesfield, UK (3 days per week on-site hybrid working) Duration - 12 months IR35 Status - Inside The Clinical Supply Study Lead (CSSL) designs and executes supply chain for one or more global clinical studies across all phases within drug development.
The CSSL holds overall accountability for delivery of IP and co-ordinates associated tasks and activities across all relevant functions within the supply chain.
The Role will have multiple contacts across internal and external groups including leadership of working groups.
There are key areas of CSSL accountability at the study level: Study Design influence : Input to Study Design Concept, Clinical Study Protocol, Handling Instructions, Pharmacy Manual or other relevant.
Works in collaboration with the Design specialist and IRT specialist teams to agree optimum SC design using the Suite (former CT-Fast) where applicable to optimize IRT settings.
Input to randomization strategy.
Stakeholder management : Lead the Study Drug Working Group to enable continuous dialogue with the clinical team on the study design requirements and their changes affecting supply chain of the study.
Contribution to the Supply Chain Team Meetings, ensuring effective collaboration with Dev QA, Analytical, CMC, SCPL
