Vaga: Vaga de Analista de Recursos Humanos em Sao Paulo/SP - home office

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Descrição Geral

Empresa localizada na cidade de São Paulo/SP do ramo Recursos Humanos, contrata Analista de Recursos Humanos.

Atribuições

As a leading global contract research organization (cro) with a passion for scientific rigor and decades of clinical development experience, fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff conducting operations in more than 90 countries, fortrea is transforming drug and device development for partners and patients across the globe. Essencial job duties responsible for all aspects of study site monitoring including routine monitoring and close-Out of clinical sites, maintenance of study files, conduct of pre-Study and initiation visits liaise with vendors and other duties, as assigned responsible for all aspects of site management as prescribed in the project plans general on-Site monitoring responsibilities ensure the study staff who will conduct the protocol have received the proper materials and instructions to safely enter patients into the study ensure the protection of study patients by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements ensure the integrity of the data submitted on case report forms (crfs) or other data collection tools by careful source document review monitor data for missing or implausible data ensure the resources of the sponsor and labcorp are spent wisely by performing the required monitoring tasks in an efficient manner, according to sops and established guidelines, including managing travel expenses in an economical fashion according to labcorp travel policy ensure audit readiness at the site level travel, including air travel, may be required and is an essential function of the job. prepare accurate and timely trip reports responsible for all aspects of registry management as prescribed in the project plans undertake feasibility work when requested participate in and follow up on qualit

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