PSI CRO AG ยท 1 day ago
Site Contract Coordinator
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Responsibilities
Review and negotiate site budgets
Facilitate the review and negotiation of clinical trial agreements (CTAs) and investigator grants between PSI Legal, the project team, and the study site.
Customize and prepare contractually binding site-specific documents in cooperation with PSI Legal.
Track CTA and investigator grant negotiation status in the Clinical Trial Management System (CTMS).
Prepare the executable version of the contract, including grants, and coordinates the signature process.
File executed contracts in the Trial Master File and maintains local documentation.
Liase with the project team, translation, and legal departments on site contracting and grant negotiation matters.
Qualification
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Required
College/University degree or an equivalent combination of education, training & experience
Minimum of 12 months experience in the clinical research industry
Knowledge and experience with legal documents related to clinical trial sites.
PC skills to be able to work with MS Word, Excel and PowerPoint
Ability to plan, multitask and work in a dynamic team environment
Communication and collaboration skills
Company
PSI CRO AG
PSI is a leading global full service contract research organization that predictably enrolls patients across multiple therapeutic areas.
Funding
Current Stage
Late StageRecent News
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