Clinical Trial Coordinator

1 dia atrás


São Paulo, São Paulo, Brasil beBeeClinicalTrial Tempo inteiro R$80.000 - R$120.000
Job Opportunity

We are seeking a professional to join our team in assisting with the design and analysis of clinical trials. As a key member, you will play a pivotal role in interpreting complex medical data and contributing to the advancement of innovative treatments and therapies.

Key Responsibilities
  • Coordinate and administer clinical trials, ensuring compliance with protocols and regulatory requirements.
  • Maintain and organize clinical trial documentation, including study files, essential documents, and regulatory submissions.
  • Prepare study-related materials, such as informed consent forms and case report forms.
  • Facilitate communication and ensure smooth trial execution through collaboration with cross-functional teams.
  • Track and report clinical trial metrics and milestones.
Requirements
  • Bachelor's degree in a scientific or healthcare-related field.
  • Prior experience with ethics submissions (CEP/CONEP).
  • Knowledge of clinical trial processes, regulations, and guidelines.
  • Excellent organizational and communication skills.
  • Ability to work collaboratively in a fast-paced environment with attention to detail.
  • Good level of English.
What We Offer

We prioritize building a diverse culture that rewards high performance and nurtures talent. Our competitive salary is complemented by additional benefits designed to enhance well-being and work-life balance opportunities for you and your family.

Some benefits include:

  • Annual leave entitlements
  • A range of health insurance offerings
  • Retirement planning offerings
  • Global Employee Assistance Programme, TELUS Health, offering access to a network of professionals for support and well-being
  • Life assurance
  • Flexible country-specific optional benefits

At ICON, we value inclusion & belonging as fundamental to our culture and values. We provide an inclusive and accessible environment for all candidates and commit to providing a workplace free of discrimination and harassment.



  • 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$40.000 - R$80.000

    Are you a diligent and detail-oriented individual with a strong understanding of clinical trials? Do you have excellent communication skills and the ability to work independently? We are seeking a Clinical Research Associate (CRA) to join our team.As a CRA, you will be responsible for coordinating all aspects of the clinical monitoring and site management...


  • São Paulo, São Paulo, Brasil beBeeStudy Tempo inteiro R$44.423 - R$65.491

    Job DescriptionThe Clinical Study Coordinator will be responsible for the setup, organization, and maintenance of clinical study documentation. This includes preparation for internal/external audits, final reconciliation, and archival.This role requires an ability to travel as needed, with at least 60% of the time dedicated to this activity. The coordinator...


  • 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 beBeeClinical Tempo inteiro R$80.000 - R$120.000

    Job OverviewWe are seeking a highly skilled professional to oversee and coordinate clinical trials, ensuring compliance with regulations and collecting and analyzing critical data.


  • São Paulo, São Paulo, Brasil beBeeClinicalResearch Tempo inteiro R$45.679 - R$64.343

    Job Overview:">Clinical Trial Assistant 1Perform daily administrative tasks in conjunction with the Clinical Research Associates and Regulatory teams to ensure a complete and accurate trial master file delivery.">Essential Functions">">Assist Clinical Research Associates (CRAs) and Regulatory teams with updating and maintaining clinical documents and systems...


  • 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...


  • São Paulo, São Paulo, Brasil beBeeProject Tempo inteiro R$76.000 - R$104.000

    Project CoordinatorWe are seeking a skilled professional to work in our Sao Paulo office. Job ResponsibilitiesProvide internal support to global Project Leaders on clinical trials.Manage project schedule setup and maintenance.Ensure resource and system access management.Maintain project tools throughout the project progress.RequirementsStrong leadership...


  • São Paulo, São Paulo, Brasil IQVIA Tempo inteiro US$40.000 - US$60.000 por ano

    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...