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- Contract and Regulatory Specialist - Single sponsor!
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Contract and Regulatory Specialist - Single sponsor!
IQVIA Holdings Inc.
Tel Aviv, Israel
Essential Functions
Ensurethe successful negotiation and ongoing management of clinical trial agreements with investigative sites and vendor agreements and associated budgetmanagement.
Maintainaccurate records, metrics and reports; identify gaps and report to management; make recommendations for process improvement andefficiencies
accountabilityfor processes or groups of trials; operates with limitedoversight
Achievessuccessful delivery of site start-up, in-house site management and closeout activities meeting internal and external clientrequirements.
Responsibleforend to endprocess withincountry
Qualifications
Bachelor Degree in Economics or equivalent, preferebly.
At least 2 years of experience in Regulatory submissions.
Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint.
Knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines as provided in company training.
Effective written and verbal communication skills including good command of English language.
Effective time management and organizational skills.
Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
Permanent position
Homebased
At IQVIA, we believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. The advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible by our 67,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way. Learn more at jobs.iqvia.com.
Job posted: 2021-04-08