Clinical trial coordinator

4 semanas atrás


São Paulo, Brasil Planet Pharma Tempo inteiro

We are seeking a dedicated and detail-oriented Clinical Trial Coordinator to join our hospital’s research team in São Paulo. This role is pivotal in managing and executing clinical trials in compliance with regulatory standards, ensuring the highest quality of patient care and data integrity.Key ResponsibilitiesCoordinate all aspects of clinical trial operations from initiation to close-outLiaise with investigators, sponsors, and regulatory bodies to ensure protocol adherenceRecruit, screen, and enroll study participants in accordance with inclusion/exclusion criteriaMaintain accurate and up-to-date trial documentation, including case report forms and source dataMonitor patient safety and report adverse events promptlySchedule and conduct study visits, ensuring compliance with Good Clinical Practice (GCP)Assist in budget planning and resource allocation for clinical studiesTrain and supervise research assistants and support staffPrepare for and participate in audits and inspectionsQualificationsBachelor’s degree in life sciences, nursing, pharmacy, or related field (Master’s preferred)Several years of experience coordinating clinical trialsStrong knowledge of ICH-GCP, ANVISA regulations, and international clinical research standardsExcellent organizational and communication skillsProficiency in Portuguese and English (written and spoken)Familiarity with electronic data capture systems and trial management software


  • Clinical Trial Coordinator

    4 semanas atrás


    São Paulo, Brasil Planet Pharma Tempo inteiro

    We are seeking a dedicated and detail-oriented Clinical Trial Coordinator to join our hospital’s research team in São Paulo. This role is pivotal in managing and executing clinical trials in compliance with regulatory standards, ensuring the highest quality of patient care and data integrity. 🧠 Key Responsibilities Coordinate all aspects of clinical...

  • Clinical Trial Coordinator

    4 semanas atrás


    São Paulo, Brasil Planet Pharma Tempo inteiro

    We are seeking a dedicated and detail-oriented Clinical Trial Coordinator to join our hospital’s research team in São Paulo. This role is pivotal in managing and executing clinical trials in compliance with regulatory standards, ensuring the highest quality of patient care and data integrity.

  • Clinical Trial Coordinator

    4 semanas atrás


    São Paulo, Brasil Planet Pharma Tempo inteiro

    We are seeking a dedicated and detail-oriented Clinical Trial Coordinator to join our hospital’s research team in São Paulo. This role is pivotal in managing and executing clinical trials in compliance with regulatory standards, ensuring the highest quality of patient care and data integrity. Key Responsibilities Coordinate all aspects of clinical trial...

  • Clinical Trial Coordinator

    4 semanas atrás


    São Paulo, Brasil Planet Pharma Tempo inteiro

    We are seeking a dedicated and detail-oriented Clinical Trial Coordinator to join our hospital’s research team in São Paulo. This role is pivotal in managing and executing clinical trials in compliance with regulatory standards, ensuring the highest quality of patient care and data integrity. Key Responsibilities Coordinate all aspects of clinical trial...

  • Clinical Project Manager

    2 semanas atrás


    Sao Paulo, Brasil CTI Clinical Trial Services, Inc Tempo inteiro

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  • São Paulo, São Paulo, Brasil MSD Tempo inteiro US$40.000 - US$80.000 por ano

    Job DescriptionUnder the oversight of the line-manager, this role is responsible for comprehensive trial and site administration and involves preparing, collating, distributing and archiving clinical documents. The CTC supports clinical supply & non-clinical supply management and ensures timely maintenance of tracking and reporting tools, as applicable.The...


  • São Paulo, São Paulo, Brasil MSD Tempo inteiro US$40.000 - US$80.000 por ano

    Job DescriptionUnder the oversight of the line-manager, this role is responsible for comprehensive trial and site administration and involves preparing, collating, distributing and archiving clinical documents. The CTC supports clinical supply & non-clinical supply management and ensures timely maintenance of tracking and reporting tools, as applicable.The...


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