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1 VAGA DE Designer EM São Paulo / SP
Função/cargo da vaga:
Designer
Empresa:
Nome da empresa disponível para cadastrados.
Salário:
A combinar
Cidade/Estado:
São Paulo / SP
Tipo de Vaga:
Home Office
Regime de contrato:
Efetivo/CLT
Descrição da vaga:
We are looking for a creative regulatory affairs consultant to join our passionate team at parexel international in são paulo, your career as a full time regulatory affairs consultant is an incredible opportunity to develop productive you are strong in critical thinking, cooperation and have the right drive for the job, then apply for the position of regulatory affairs consultant at parexel international today!Regulatory affairs consultant must have an understanding of the organizations consulting models and methodologies, as well as good knowledge of what services pc provides. The consultant must have strong technical skills and may be developing specialist knowledge of a particular subject and/ or market. This key role in the organization ensures the timely performance of work within a project scope to the quality expectations of pc and the client. When serving as a project lead or work stream lead, a consultant secures the work of the entire team or work stream is delivered on time and that it meets clients and pcs quality expectations. Skills and knowledge:regulatory affairs consultant should have solid local expertise in submitting clinical trials to health authority in role will be responsible for managing and coordinating the regulatory submission strategy for a large number of clinical trials in brazil. Also, will coordinate and manage flow of information, track project progress, and identify and solve problems in a team-Oriented part of the more relevant tasks, it will review critical key technical documents (e.G. Clinical trial protocols and reports, study drug labels, and other clinical trial related technical documentation) to ensure regulatory compliance for clinical trial applications, consistency with other key documents and ease of review. The consultant supports the sponsor for the development of optimized clinical trial submission strategies. Good communication and leadership skills as well as team player attitude is needed to be successful in this position. Detail orientation and flexibility will be highly appreciated as well. We are looking for candidates with experience in these activities developed in cro or similar organizations. Benefits of working as a regulatory affairs consultant in são paulo, sp:? Excellent benefits? Company offers career progression opportunities? Advantageous package.
Cód. 9966297
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