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Word Processing Jobs In Rio De Janeiro - 9 Job Positions Available

1 – 7 of 9 jobs
Wilhelmsen group jobs

Join our global team for a career filled with opportunities to solve challenges both small and large, local and global, simple and complex. Main responsibilities Position-holder is responsible for: Registering supplier invoice data into accounting system

Wilhelmsen Group  27 days ago
American Bureau of Shipping jobs

The Collections Specialist is responsible for identifying and resolving delinquent accounts and maintaining due diligence of account collection activities to assist in support of the accounting. What You Will Do: Monitor accounts to identify outstanding debts

American Bureau Of Shipping  24 days ago
Thermo Fisher Scientific jobs

Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Join Us as a Clinical Trial Coordinator – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750

Thermo Fisher Scientific  6 days ago

Essential Job Functions - Assist in processing purchase orders, verifying their accuracy, and ensuring compliance with procurement policies and procedures; - Update internal and external Expediting Software; - Monitor purchase order status and expedite delivery as necessary

Crane Worldwide Logistica Do Brasil Ltda  2 days ago
Moritz jobs

About Moritz Moritz is an AI-native global law firm building the next generation of commercial legal infrastructure. We combine proprietary AI tooling with a curated network of senior commercial lawyers to deliver vetted contract work at

Moritz  22 hours ago
Moritz jobs

About Moritz Moritz is an AI-native global law firm building the next generation of commercial legal infrastructure. We combine proprietary AI tooling with a curated network of senior commercial lawyers to deliver vetted contract work at

Moritz  22 hours ago
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Worldwide Clinical Trials jobs

What the Associate II, Pharmacovigilance does at Worldwide Responsible for the collection, processing, evaluation and reporting of incoming Serious Adverse Event (SAE) data according to applicable regulatory guidelines/requirements, Worldwide Standard Operating Procedures (SOPs) and project specific instructions.

Worldwide Clinical Trials  22 hours ago

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