Clinical Research Associate 2

2 semanas atrás


Oeiras, Portugal IQVIA Tempo inteiro

Clinical Research Associate Your responsibilities will include: Performing site selection, initiation, monitoring and close-out visits Supporting the development of a subject recruitment plan Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.E., Good Clinical Practice and International Conference on Harmonization guidelines Managing progress by tracking regulatory submissions, recruitment, case report



  • Oeiras, Portugal Fortrea Tempo inteiro

    Clinical Research Associate 2 - FSO Model - Portugal Join to apply for the Clinical Research Associate 2 - FSO Model - Portugal role at Fortrea. Job Overview Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. Ensures the implementation of...


  • Oeiras, Lisboa, Portugal IQVIA Tempo inteiro

    Clinical Research AssociateYour Responsibilities Will IncludePerforming site selection, initiation, monitoring and close-out visitsSupporting the development of a subject recruitment planEvaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice and International Conference on Harmonization...


  • Oeiras, Portugal IQVIA Tempo inteiro

    Clinical Research Associate needed in Porto to perform site visits and support recruitment plans.


  • Oeiras, Portugal IQVIA Tempo inteiro

    A leading global provider of clinical research services is looking for a Clinical Research Associate based in Porto. This entry-level, full-time role requires performing site selection, initiation, monitoring, and close-out visits while supporting the development of subject recruitment plans. Applicants should hold a relevant university degree and possess...


  • Oeiras, Portugal IQVIA Tempo inteiro

    Senior Clinical Research Associate Your responsibilities will include: Performing site selection, initiation, monitoring and close-out visits Supporting the development of a subject recruitment plan Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.E., Good Clinical Practice and International Conference on...


  • Oeiras, Portugal MSD Tempo inteiro

    Job Description We are one of the leading pharmaceutical companies in the world, dedicated to the discovery, development, and delivery of innovative medicines that improve health and quality of life for people. With a strong global presence and an unwavering commitment to scientific research, our mission is to transform health through innovation and...


  • Oeiras, Portugal MSD Portugal Tempo inteiro

    Job DescriptionWe are one of the leading pharmaceutical companies in the world, dedicated to the discovery, development, and delivery of innovative medicines that improve health and quality of life for people. With a strong global presence and an unwavering commitment to scientific research, our mission is to transform health through innovation and...


  • Oeiras, Portugal Fortrea Tempo inteiro

    Job Overview: Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. Assures the implementation of project plans, as assigned. Summary of Responsibilities: Responsible for all aspects of study site monitoring including routine monitoring and...


  • Oeiras, Lisboa, Portugal Fortrea Tempo inteiro

    Job Overview:Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. Assures the implementation of project plans, as assigned.Summary of Responsibilities:Responsible for all aspects of study site monitoring including routine monitoring and closeout...


  • Oeiras, Portugal IQVIA Tempo inteiro

    Job Description We are seeking a highly skilled Clinical Research Associate (CRA) to lead performance and compliance for assigned protocols and sites within Portugal - Zona Norte . Under the oversight of the CRA Manager, you will serve as the primary site contact throughout all phases of clinical studies, ensuring rigorous adherence to ICH/GCP, local...