Job Description
Labcorp Drug Development is looking for a Contract Specialist II to focus in Site Agreements.
About the Job
This is a full time client-dedicated position to work 50% in the client's Middlesex office and 50% from home. As such, candidates will need to be based in and around the London area or in south/south-east England within commutable distance of Uxbridge.
In essence what we're looking for here is someone who really enjoys negotiating contracts for commercial pharmaceutical-sponsored Clinical Trials!
Ideally we are looking for an experienced clinical research professional with a working knowledge of clinical trial start-up, budgeting (negotiation, invoicing and payments) and/or contract negotiation. The successful individual will be responsible for the end-to-end management of budgeting and executing Clinical Trial Agreements with investigator sites with a focus on preparing contracts for a variety of commercial client-sponsored clinical trials including Confidential Disclosure Agreements (CDAs), Master Service level agreements and Investigator contracts for non-registration al /Investigator Sponsored Research studies. You will be responsible for contract amendments as well as original contracts. In this role, you will be expected to work across contracts in UK, Ireland, Belgium and Netherlands.
To be successful in this role, you will need to have strong organization and time management skills and the ability to effectively manage multiple competing priorities. You will need excellent communication skills with an ability to communicate with colleagues at all levels across the organization and with external partners at site, including R&D contacts, study investigators. Your negotiation and interpersonal skills, including strong conflict resolution skills will also be key for this role.
Other Information: This role is a full time & permanent position to be employed through Labcorp. For more information please contact Andy Smith at Covance on or mail
Key words: Clinical Research, Contracts Specialist Clinical Research Associate, Middlesex, Berkshire London GCP, Pharmaceutical, Middlesex, Berkshire, London, Study Start-up, Clinical research contracts
Education
- B achelor's degree required preferably within life sciences or equivalent (eg Finance, legal with an understanding of the clinical trial process).
Experience
Two or more years' experience negotiating legal or financial agreements, preferably in the pharmaceutical industry / CRO OR two years of industry /hospital site experience in clinical operations
Working knowledge of clinical trial start-up and finance cycles including knowledge of site needs and perspective
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