Study Coordinator

3 semanas atrás


Lisboa, Lisboa, Portugal CUF - Hospitais e Clínicas Tempo inteiro
Somos uma empresa 100% portuguesa, líder na prestação de cuidados de saúde de excelência em Portugal, que conta com mais de 75 anos de experiência e uma rede de 23 Hospitais e Clínicas CUF distribuídas pelo país

Baseamo-nos em valores como:
o Respeito, a Dignidade, o Bem-Estar das Pessoas, a Integridade, o Desenvolvimento Humano, a Competência e a Inovação.

Queremos atrair os melhores profissionais para colaborarem numa organização líder de mercado, que trabalha diariamente para atingir a excelência. Estamos a recrutar um
Coordenador de Estudos Clínicos, para o Hospital CUF Descobertas.

Local de Trabalho:
Hospital CUF Descobertas, Parque das Nações.

Missão:

Acompanhar e dar suporte às equipas de investigação, na condução de estudos clínicos (ensaios clínicos e estudos observacionais) desenvolvidos pela indústria, e contribuir para o desenvolvimento da investigação interna.


Quais as principais responsabilidades do Coordenador de Estudos Clínicos?**- Assegurar o acompanhamento dos Estudos Clínicos (ensaios clínicos e estudos observacionais) e projectos de investigação na CUF;

  • Divulgar internamente os projetos e confirmar a possibilidade de participação de todos os serviços envolvidos nos estudos sob a sua coordenação;
  • Divulgar os critérios de inclusão e exclusão dos ensaios para recrutamento interno e referenciação de clientes;
  • Participar nas reuniões de qualificação do Centro/Unidade;
  • Registar na Base de Dados/ficheiros do Centro a actividade realizada no prazo instituído;
  • Assegurar a formação dos investigadores, enfermeiros, farmacêuticos, técnicos de acordo com o protocolo do ensaio;
  • Recolher e atualizar toda a documentação necessária ao processo de submissão;
  • Preparar informação relativa ao ensaio para submissão à DPO e Comissão de Ética e Jurídica;
  • Preencher os CRFs (Case Report Forms) de acordo com o processo clínico do cliente e proceder ao respetivo envio em plataforma do ensaio clínico, incluindo resposta a discrepâncias;
  • Identificar a informação em falta no processo, e assegurar a atualização da mesma em processo clínico pelo profissional responsável;
  • Arquivar a documentação no dossier do Investigador e assegurar a sua manutenção com os documentos atualizados tendo em conta emendas e adendas;
  • Organizar o procedimento de reembolso de despesas de cada participante incluído no Ensaio Clínico, acedendo aos seus dados;
  • Garantir o envio de colheitas/amostras solicitadas pelo promotor de acordo com protocolo;
  • Garantir a melhoria contínua dos processos, procedimentos e soluções.

O que valorizamos?

  • Experiência profissional mínima de 1 ano em funções similares;
  • Ensino superior em áreas relevantes (Ciências Farmacêuticas, Biologia, Biomédica e similiares);
  • Estágio Mestrado Investigação Clínica;
  • Conhecimento de Inglês;
  • Conhecimento de (GCP) Good Clinical Practice.
-
Experiência prévia como Study Cooordinator;:


  • Chefe de equipa;

O que pode esperar de nós?

  • Contrato de trabalho direto com a CUF;
  • Formação inicial e contínua, através da CUF Academic Center;
  • Valorização dos nossos recursos humanos através do crescimento e reconhecimento dentro da empresa (Gestão de Desempenho, Mobilidade Interna, entre outros);
  • Entidade familiarmente responsável, reconhecendo a importância da conciliação entre a vida profissional, pessoal e familiar, com oferta de benefícios nesse sentido (apoios para nascimentos, cabaz escolar, 40h anuais para realização de voluntariado, bolsas para frequência do ensino superior, entre muitos outros).
**Quer juntar-se à equipa CUF?

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