Vagas de Associate em Sergipe

Company DescriptionBlueOak is a structured credit and structured private equity asset management firm.Role Description This is a full-time on-site role for an Analyst / Associate at BlueOak Investments. The role is located in São Paulo, SP. The Analyst / Associate will be responsible for conducting

SOFAR

We are looking for an experienced and self-driven professional to join our team and support the development ofC&I PV inverter and energy storage solutions. Responsibilities Analyze local market trends, customer needs, and application scenarios for C&I PV and ESS products; Provide pre-sales technical

DHL Global Forwarding

About DHL The logistics company for the world! Connecting People. Improving Lives. Our specialized DHL divisions offer an unparalleled portfolio of logistics services and solutions ranging from domestic and international parcel delivery and e-commerce shipments to air, sea and road freight services

High5

Clinical Research Associate IISão Paulo, Brazil Full TimeAbout Us:Join our team and help shape the future of our organization. We are a leading company committed to excellence and innovation, seeking a talented Senior Recruiter to support our growth. Job Overview:Perform monitoring and site manageme

Excent Capital Ltd

Quem SomosA Excent Capital é um grupo financeiro global e regulamentado, fundado em 2021 e construído por profissionais com mais de uma década de experiência nos mercados financeiros. Atuamos em Londres, Seychelles, Limassol, Cidade do México e São Paulo, com tecnologia 100% própria, licenciamento i

Tech Mahindra

Role - Sr. Business Associates (Account Receivables)Exp - 8-15 yrsJob Description -Managing Customer Invoices and Billings for Brazil customers and Intercompany billing. Billing types will be both services and goods. Monitoring and Collecting Payments within due dates for effective cash management R

Digisystem

Profissional responsável por liderar tecnicamente a evolução da Plataforma de CRM, atuando como referência em arquitetura de dados e integrações, com forte entendimento de negócio. Deve apoiar o time nas decisões técnicas, garantir boas práticas de engenharia e viabilizar soluções escaláveis, confiá

Prisma Capital (Brasil)

Prisma Capital is strengthening its Capital Formation team and hiring an Associate III focused on fundraising and investor coverage for our onshore credit strategies. This is a high-impact, front-office role for professionals with experience in DCM, credit sales or distribution, looking to operate c

Astecha

Descrição do CargoAs maiores gestoras, fundos e securitizadoras do Brasil estão em plena transformação tecnológica — e descobrindo que IA só funciona quando há dados e processos automatizados integrados.A Astecha é a plataforma de automação e IA para o mercado de capitais brasileiro. Conectamos APIs

JoVE

JoVE is the world- leading producer and provider of video solutions with the mission to improve scientific research and education. Millions of scientists, educators and students use JoVE for their research, teaching and learning. Our institutional clients comprise over 1,000 universities, colleges,

INDI Staffing Services

At INDI, we're passionate about empowering individuals and businesses worldwide. Our cutting-edge recruiters connect leading companies with top talent, fostering a dynamic environment where innovation thrives. Join us in shaping the future of work. Overview of the role: We are looking for a Tale

Worldwide Clinical Trials

What the Associate II, Pharmacovigilance does at WorldwideResponsible 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

Worldwide Clinical Trials

What the Associate II, Pharmacovigilance does at WorldwideResponsible 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

Worldwide Clinical Trials

What the Associate II, Pharmacovigilance does at WorldwideResponsible 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

Worldwide Clinical Trials

What the Associate II, Pharmacovigilance does at WorldwideResponsible 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

Worldwide Clinical Trials

What the Associate II, Pharmacovigilance does at WorldwideResponsible 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

Worldwide Clinical Trials

What the Associate II, Pharmacovigilance does at WorldwideResponsible 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

Worldwide Clinical Trials

What the Associate II, Pharmacovigilance does at WorldwideResponsible 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

Worldwide Clinical Trials

What the Associate II, Pharmacovigilance does at WorldwideResponsible 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

Worldwide Clinical Trials

What the Associate II, Pharmacovigilance does at WorldwideResponsible 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