Desculpe, a oferta não está disponível,
mas você pode realizar uma nova pesquisa ou explorar ofertas semelhantes:

Research Specialist

Are you passionate about uncovering insights that drive business strategy and decision-making? Do you thrive on diving deep into data to understand behaviour...


Hays - São Paulo

Publicado 3 days ago

Pesquisador Júnior - Materiais Inorgânicos

Venha fazer parte do time de Pesquisa e Desenvolvimento da Saint Gobain! SOBRE O GRUPO SAINT-GOBAIN Com mais de 350 anos de história, o grupo francês é líder...


Saint Gobain - São Paulo

Publicado 3 days ago

Analista Pesquisa Mercado Pleno

Kantar é a empresa líder mundial em dados, percepções e consultoria. Ajudamos os nossos clientes a compreender as pessoas e a inspirar o seu crescimento Proc...


Insights By Kantar - São Paulo

Publicado 3 days ago

Analista De Desenvolvimento De Produtos - Cotia/Sp

O Analista de Desenvolvimento de Produto (Engenharia-Pleno) na Southco será responsável por criar e desenvolver desenhos técnicos detalhados de produtos, col...


Southco, Inc. - São Paulo

Publicado 3 days ago

Research Assistant: Maceió, Brazil - Fix Term And Part Time

Detalhes da Vaga

Are you looking for an opportunity in Clinical Research? Do you want to work for an industry-leading company that offers you experience and supports career progression whilst giving you the option of working flexibly? If so, come and join us - IQVIA is looking for a Clinical Research Coordinator.This role has an immediate start working 20 hours a week for a period of 6 months to support the site. The study coordinator should have experience clinically or a nursing background as tasks include performing EKGs and collecting vital signs.As a pivotal member of the site team, you will be involved with a variety of administrative tasks to support investigators and ensure the smooth running of clinical trials and assist with collecting patient data.Day-to-day responsibilities will include:Verifying and/or correcting research study information on source documents; researching queries and variances; providing feedback to the site data collector.Accurate input of trial data into the Electronic Data Capture (EDC) system and tracking visits and procedures completed against budget in the clinical trial management system (CTMS).Preparing and maintaining study files, and timely submission of information.Collecting, submitting and assisting in maintaining relevant regulatory and ethics documents.Scheduling visits with research subjects, generating appropriate reports and documentation.Other administrative support functions such as reception, office organization, and supply management.We are looking for candidates with the following skills and experience:BS/BA in life sciences or educational equivalent and/or relevant work experience in a clinical environment or medical setting, e.g., clinical research coordinator, nurse, medical assistant, or other medical profession.Basic knowledge of clinical trials, combined with in-depth knowledge of departmental, protocol, and study-specific operating procedures, consent forms, and study schedules.Basic knowledge of medical terminology.Strong IT competence, skilled in using MS Windows and Office applications such as Access, Outlook, Excel, and Word.Excellent interpersonal skills with the ability to establish and maintain effective working relationships with co-workers, managers, and clients.Good organizational skills with the ability to pay close attention to detail.IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com.
#J-18808-Ljbffr


Salário Nominal: A acordar

Fonte: Whatjobs_Ppc

Função de trabalho:

Requisitos

Built at: 2024-11-17T01:02:25.505Z