Clinical Study Manager

2 semanas atrás


Porto, Portugal iLoF Tempo inteiro

Manages clinical studies, ensures regulatory compliance, and collaborates with external partners to advance personalized medicine.



  • Porto, Portugal iLoF Tempo inteiro

    Company Description Hello We're looking for an awesome Clinical Study Manager to join our team on our journey to revolutionize personalized medicine. Job Description About your Role Plan, execute, and close out clinical studies (domestic and international) to the highest standards of quality, ethics, and regulatory compliance. Build and manage collaborations...


  • Porto, Portugal iLoF Tempo inteiro

    **Company Description** Hello!** We're looking for an awesome Clinical Study Manager to join our team on our journey to revolutionize personalized medicine. **Job Description** About your Role** - Plan, execute, and close out clinical studies (domestic and international) to the highest standards of quality, ethics, and regulatory compliance. - Build and...


  • Porto, Portugal iLoF Tempo inteiro

    Hello!We're looking for an awesome Clinical Study Manager to join our team on our journey to revolutionize personalized medicine.About your RolePlan, execute, and close out clinical studies (domestic and international) to the highest standards of quality, ethics, and regulatory compliance.Build and manage collaborations with external partners and clinical...


  • Porto, Portugal Bial Tempo inteiro

    **MISSION**: Support and monitor the clinical trial operations activities from phase I to phase IV sponsored by BIAL, according to the Clinical Development Plan. **MAIN ATTRIBUTIONS AND RESPONSABILITIES**: - Support on clinical trials implementation: identification of third party’s vendors (e.g., CROs; bioanalytical/central/genetics labs), review of...


  • Porto, Portugal Descompagnons Trabalho Temporário Lda Tempo inteiro

    A leading health technology firm in Porto seeks a Clinical Operations Manager to oversee clinical studies and ensure the highest standards of quality and regulatory compliance. The role involves managing external partnerships, maintaining ethical approvals, and safeguarding participant data. Candidates should have significant experience in clinical...


  • Porto Salvo, Portugal IQVIA Tempo inteiro

    Project Leads are an integral part of clinical trial delivery, liaising with clinical teams to improve patients' lives by bringing new drugs to the market faster. The Project Lead is an essential member of the core project team responsible for project delivery of clinical studies to meet contractual requirements in accordance with SOPs, policies and...

  • Clinical Research Physician

    1 semana atrás


    Porto, Portugal Bial Tempo inteiro

    **Join Our Mission to Improve Lives Worldwide** Designs and medically monitors clinical studies, according to the clinical development plan, in order to assure the delivery of state-of-the-art medical and scientific results, as well as safeguarding the safety, rights and welfare of study participants and the scientific integrity of research results. **The...

  • Clinical Research Associate

    3 semanas atrás


    Porto, Portugal Meet Life Sciences Tempo inteiro

    Freelance Clinical Research Associate 0.3 FTE 18 Month Study Medical Device & Submissions Experience Required

  • Clinical Research Associate

    3 semanas atrás


    Porto, Portugal Meet Life Sciences Tempo inteiro

    Freelance Clinical Research Associate 0.3 FTE 18 Month Study Medical Device & Submissions Experience Required

  • Clinical Research Associate

    3 semanas atrás


    Porto, Portugal Meet Life Sciences Tempo inteiro

    Freelance Clinical Research Associate 0.3 FTE 18 Month Study Medical Device & Submissions Experience Required