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.
Senior Clinical Vendor Specialist - BioSamples/Central Laboratory - Remote - FSP
Job ID R0000036507 , United KingdomParexel FSP are currently recruiting for a Senior Clinical Vendor Specialist in the UK. This is a 100% remote position and is dedicated to one of our key global sponsors.
In this position you will be an invaluable resource working closely with line manager, and other key personnel to implement and operationalize the departments goals within client clinical trials.
Manages central laboratory and specialty vendors across a mix varyingly complex clinical trial. Performs other duties as necessary to ensure optimal clinical trial execution.
Some specifics about this advertised role
100% homebased position
Manages acquisition of clinical trial samples
Provides support for sample related matters to clinical study teams
Works with ICF Specialist and wider team to ensure compliance with ICF permissions
Assists with vendor selection and oversight
Provides input to clinical trial related documents under the supervision of the Lead
Executes biomarker plans in collaboration with the study team and Lead
Prepares request for proposals, reviews and assess bids and Statement of Work (SOW).
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 the 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.
Minimum of 6 years relevant industry experience is required.
Science background and working knowledge of a wide array of medical terms, biological assays including proteomics, cellular assays and genomics.
Understanding of bioethics of human biospecimen collection and research
Oncology experience preferred.
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