Clinical Trials Coordinator

2 semanas atrás


São Paulo, São Paulo, Brasil beBeeResearch Tempo inteiro US$91.336 - US$114.170

Clinical Research Associate Job Description:

We are seeking an experienced Clinical Research Associate to manage all aspects of site evaluation, initiation, monitoring, and close-out for clinical trials. As a key member of our team, you will be responsible for ensuring trial conduct adheres to regulatory requirements.

Key Responsibilities:

  • Manage site evaluation, initiation, monitoring, and close-out for multiple studies across various sites.
  • Ensure compliance with ICH GCP, FDA regulations, SOPs, and protocol requirements.
  • Develop and implement recruitment strategies to meet enrollment targets in collaboration with sites.
  • Monitor and document adverse event and serious adverse event reporting to ensure patient safety.
  • Train and retrain site personnel on study protocols, systems, and operational procedures.
  • Maintain audit-ready documentation and reconcile with the Trial Master File.
  • Identify and resolve site performance, quality, or compliance issues with effective intervention plans.

Requirements:

  • Bachelor's degree in Life Sciences or Registered Nurse (RN).
  • Minimum 2 years of on-site monitoring experience in Oncology, specifically solid tumor trials.
  • Experience with Graft-Versus-Host Disease (GVHD) studies.
  • Ability to conduct regional travel up to 8–10 days per month.
  • Valid driver's license and ability to travel regularly.
  • Proficient in EDC, CTMS, IVRS, and Microsoft Office Suite.
  • Knowledgeable in ICH GCP, HIPAA, FDA CFR, and other applicable guidelines.

  • Clinical Trial Coordinator

    2 semanas atrás


    São Paulo, São Paulo, Brasil beBeeClinicalTrialCoordinator Tempo inteiro R$72.000 - R$108.000

    We are seeking a Clinical Trial Coordinator to support the administration of clinical trials.Key Responsibilities:Ensure compliance with trial protocols and regulatory requirements.Maintain organized documentation, including study files and essential documents.Support the preparation of trial-related materials.Collaborate with cross-functional teams for...


  • São Paulo, São Paulo, Brasil beBeeResearch Tempo parcial

    **Job Summary:**We are seeking a skilled Clinical Research Coordinator to join our team. In this role, you will be responsible for coordinating clinical trials and ensuring their smooth execution.About the Role:The Clinical Research Coordinator will work closely with investigators, research staff, and other stakeholders to coordinate all aspects of clinical...


  • São Paulo, São Paulo, Brasil beBeeClinical Tempo inteiro R$59.020 - R$104.940

    Job OverviewWe are seeking a skilled and experienced Senior Clinical Trials Coordinator to join our team. In this vital role, you will be responsible for managing clinical trials from start-up to close-out, ensuring the quality and scientific integrity of our research.Key Responsibilities:Study Management: Partner with cross-functional teams to plan, manage,...


  • São Paulo, São Paulo, Brasil beBeeProject Tempo inteiro R$80.000 - R$120.000

    About the Role">We are seeking an experienced Project Coordinator to assist project managers in planning, executing and monitoring clinical trials.The successful candidate will coordinate study activities including site selection, patient recruitment and data collection. They will also support the development of study protocols, case report forms and other...


  • São Paulo, São Paulo, Brasil Iqvia Tempo inteiro

    Are you looking for an opportunity in Clinical Research?Do you want to work for an industry leading company that offers you experience and supports career progression whilst giving you the option of working flexibly?If so, come and join us - IQVIA are looking Clinical Research Coordinator.This role has an immediate start working 40 hours a week for a period...

  • Clinical Trials Coordinator

    2 semanas atrás


    São Paulo, São Paulo, Brasil beBeeClinicalResearchAssociate Tempo inteiro R$65.000 - R$97.000

    Clinical Research Associate RoleFortrea seeks a skilled professional to oversee clinical studies, conduct site monitoring duties, and ensure data integrity. This role involves implementing Standard Operating Procedures (SOPs), adhering to International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) guidelines, and...


  • São Paulo, São Paulo, Brasil BZL IQVIA RDS Brasil Ltda Tempo inteiro

    Are you looking for an opportunity in Clinical Research? Do you want to work for an industry-leading company that offers experience and supports career progression, with flexible working options? If so, join us - IQVIA is looking for a Clinical Research Coordinator.This role has an immediate start, working 40 hours a week for a period of 4 months to support...


  • São Paulo, São Paulo, Brasil beBeeResearch Tempo inteiro

    Job OverviewWe are seeking a dedicated Clinical Research Associate (CRA) to play a key role in ensuring the successful execution of clinical trials. In this position, you will be responsible for monitoring and managing clinical sites to ensure compliance with study protocols, regulatory requirements, and sponsor expectations.Your work will directly...

  • Clinical Project Coordinator

    2 semanas atrás


    São Paulo, São Paulo, Brasil beBeeClinicalProjectCoordinator Tempo inteiro R$72.000 - R$96.000

    Job Title:Clinical Project Coordinator RoleAbout the Job:This role is designed for individuals who want to work in clinical project management, supporting teams in achieving project goals and quality standards. The Clinical Project Coordinator will assist senior project managers in various aspects of project coordination, ensuring timely completion and...


  • São Paulo, São Paulo, Brasil beBeeResearch Tempo inteiro

    Clinical Research Associate Role">We are seeking a detail-oriented and organized Clinical Research Associate to join our team. The successful candidate will be responsible for ensuring the smooth execution of clinical trials, from start-up to close-out.">Key Responsibilities:">">Provide administrative support to the trial manager in tracking progress,...