Jobs at Parexel
Are you ready to make your mark in the healthcare industry using your ingenuity and technical expertise? At Parexel, there's no limit to what you can accomplish. We work with the top 50 global pharmaceutical companies, the top global biotech companies, and hundreds of small and emerging companies. We've supported the development of some of the most important treatments of our time, including nearly all of the 50 top selling drugs currently on the market. Join us and you'll make a profound difference in millions of lives. With a role in our Information Technology group, you'll work with cutting-edge technology on internal and client-facing projects. Collaborating with people from all over the world and touching everything from enterprise systems and clinical applications to infrastructure and networking, you'll keep our data safe and confidential. You'll have the chance to develop your skills and pursue advancement opportunities that include managerial and technical tracks. If you have stellar coding and design experience and a passion to learn more about healthcare, Parexel invites you to discover our rewarding opportunities in Enterprise Architecture, Software Development, Project Management and Business Analysis, and more. In a global clinical trial environment, business-focused applications, connectivity, and data security are critical to a trial's outcome. Find out how you can be an invaluable part of our success story.
Clinical Vendor Manager - Central Labs
Job ID R0000030201 , United KingdomParexel is currently seeking an experienced clinical research professional to join us, you be assigned to one of our key sponsors in the region, as a Vendor Stat Up Manager assigned to the Central Labs category.
Working as a Vendor Start Up Manager role, you will be independently accountable for flawless and accelerated vendor service delivery at the trial start-up phase whilst supporting the 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
Dedicated to one client.
Reviewing of the vendor and category related specific sections of the protocol, ensure vendor expertise is leveraged when refining specifications towards Final Protocol
Ensures changes to protocol or study designs are consistently shared with vendors and incorporated into supplier budgets, timelines, and specifications. Supports amendment of vendor contracts with Procurement team
Optimizing a frontloaded and timely study start-up process in support of a timely vendor database-go-live
Vendor service excellence at study level, ensures vendors meet quality and service level standards in their service delivery for the trial
Pro-actively creates and maintains vendor related risk maps with contingency plan for documentation in Facilitated Issue and Risk Surveillance Tool
Here are a few requirements specific to this advertised role.
- Bachelor’s degree or equivalent degree is required, with advanced degree preferred.
- 3+ years’ experience working with Central laboratories and specialty labs.
- Excellent knowledge of the clinical operation processes and vendor management
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