Clinical Vendor Manager - Clinical Supply - Remote - FSP
United Kingdom, RemoteAdditional Locations: Ireland-Remote; ID de la oferta R0000034455 Categoría Procurement
sobre este trabajo
Parexel are currently recruiting for an experienced Clinical Vendor/Clinical Supply manager, to join one of a large Sponsor’s in the EU. This role has a focus on clinical supplies relating to radioactive materials and working with vendors across the global.
This role enables a flawless and accelerated vendor service delivery at the trial start-up phase and supports implementation of defined category strategies and service standardization.
This role proactively assesses risk and concludes contingency plans to de-risk study startup.
Some specifics about this advertised role
- Reviewing of the vendor and category related specific sections of the protocol, ensure vendor expertise is leveraged when refining specifications towards Final Protocol
- Contributing to development of Study Specification Worksheet to facilitate bid process and selection of Vendors.
- Quote/Proposal review in collaboration with procurement (and vendor). If required, support contract negotiations.
- Vendor budget review of final quotes
- Accountable for Vendor cost control, budget review, invoice reconciliation and PO close-out
Who are Parexel
Parexel supports clinical studies across the full range of therapeutic areas, and we have longstanding partnerships with a vast client base.
We supported the trials of most of today’s top 50 best-selling drugs, but equally we enable more niche drug developments that are critical to the well-being of many patients.
You’ll be an influential member of the wider team.
What we are looking for in this role
For every role, we look for professionals who have the determination and courage always to put patient well-being first.
That to us is working with heart.
Here are a few requirements specific to this advertised role.
- 3+ years working experience and excellent knowledge of the clinical operation processes and vendor management
- Excellent knowledge of GxP and ICH regulations
- Expert knowledge of clinical trial design and mapping to supplier requirements
- Experience in User Acceptance testing (eCOA & IRT)
- Knowledge of key deliverables that impact green light milestones and vendor readiness
- Experience in outsourcing, contracting, sourcing of clinical services with Vendor/CROs (RFP, RFQ, contracting)
- Specific category expertise – ideally experience of global equipment supply and/or Radiation
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