Empregos atuais relacionados a Senior Clinical Research Associate - São Paulo, São Paulo - Icon Plc


  • São Paulo, São Paulo, Brasil CTI Clinical Trial Services, Inc Tempo inteiro

    Senior Clinical Research Associate LeaderWe are committed to maintaining our company culture across all regions, especially with our remote employees, as it is crucial to our overall success.To achieve this, we hold weekly all-staff meetings where each department shares updates on their studies and milestones.Additionally, employees can participate in our...


  • São Paulo, São Paulo, Brasil CTI Clinical Trial Services, Inc Tempo inteiro

    Principal Clinical Research AssociateWe are seeking a highly skilled Principal Clinical Research Associate to join our team at CTI Clinical Trial Services, Inc. As a key member of our organization, you will play a crucial role in maintaining our company culture across all regions, particularly with our remote employees.Our company values open communication...


  • São Paulo, São Paulo, Brasil ICON Tempo inteiro

    Role OverviewWe are seeking a highly skilled Clinical Research Associate to join our team at ICON plc, a world-leading healthcare intelligence and clinical research organization. As a Clinical Research Associate, you will be responsible for providing clinical research support to our clients, ensuring the highest quality of service delivery.Key...


  • São Paulo, São Paulo, Brasil Cti Clinical Trial Services, Inc Tempo inteiro

    Job SummaryClinical Trial Services, Inc. is seeking a highly skilled Clinical Research Associate Lead to join our team. As a Clinical Research Associate Lead, you will be responsible for overseeing the conduct of clinical trials at assigned sites, ensuring compliance with regulatory requirements, and providing guidance to site staff.Key...


  • São Paulo, São Paulo, Brasil PSI Tempo inteiro

    Job Title: Lead Clinical Research AssociateJob Summary:In this role, you will oversee local clinical research activities, ensuring the protection of trial subjects' rights, safety, and well-being, as well as data quality and study compliance on a country/regional level.Key Responsibilities:Facilitate regional projects as Lead Clinical Research Associate and...

  • Clinical Research Associate

    1 semana atrás


    São Paulo, São Paulo, Brasil Thermo Fisher Scientific Tempo inteiro

    Clinical Research Associate Job DescriptionAt Thermo Fisher Scientific, we are seeking a highly skilled Clinical Research Associate to join our team. As a Clinical Research Associate, you will be responsible for ensuring the integrity and quality of clinical trials. Your primary focus will be on monitoring and managing clinical trials, ensuring compliance...


  • São Paulo, São Paulo, Brasil CTI Clinical Trial Services, Inc Tempo inteiro

    Key Responsibilities:As a Clinical Research Associate Lead at CTI Clinical Trial Services, Inc, you will serve as the main point of contact for assigned study sites, conducting site visits and completing site visit deliverables with quality and within given timelines. You will also assist with or oversee study start-up activities, including feasibility,...

  • Clinical Research Associate

    3 semanas atrás


    São Paulo, São Paulo, Brasil ICON Tempo inteiro

    About ICONICON is a leading provider of drug and device development solutions. Our team of experts is dedicated to accelerating the development of life-changing treatments.Job SummaryWe are seeking a Clinical Research Associate to join our team. As a Clinical Research Associate, you will contribute to the success of our clinical trials by ensuring the...

  • Clinical Research Associate

    3 semanas atrás


    São Paulo, São Paulo, Brasil Novasyte Tempo inteiro

    Job OverviewWe are seeking a highly skilled Clinical Research Associate to join our team. As a Clinical Research Associate, you will be responsible for ensuring that sites are conducting studies and reporting data as required by the study protocol, applicable regulations, and sponsor requirements.Key Responsibilities:Perform site monitoring visits to ensure...

  • Clinical Research Associate

    3 semanas atrás


    São Paulo, São Paulo, Brasil ICON Tempo inteiro

    Job Title: Clinical Research AssociateAt ICON, we are seeking a highly skilled Clinical Research Associate to join our team. As a Clinical Research Associate, you will play a critical role in the success of our clinical trials by ensuring the integrity of data and compliance with regulatory requirements.Key Responsibilities:Monitoring and Data Management:...

  • Clinical Research Associate

    4 semanas atrás


    São Paulo, São Paulo, Brasil ICON Tempo inteiro

    Job Title: Clinical Research AssociateAt ICON, we are seeking a highly skilled Clinical Research Associate to join our team. As a Clinical Research Associate, you will play a critical role in the success of our clinical trials by ensuring the integrity of our data and compliance with regulatory requirements.Key Responsibilities:Monitoring and Data...


  • São Paulo, São Paulo, Brasil CTI Clinical Trial Services, Inc Tempo inteiro

    Job SummaryWe are seeking a highly experienced Principal Clinical Research Associate to join our team at CTI Clinical Trial Services, Inc. As a key member of our site management team, you will be responsible for ensuring the successful execution of clinical trials at assigned study sites.Key ResponsibilitiesServe as the primary point of contact for assigned...

  • Clinical Research Associate

    1 semana atrás


    São Paulo, São Paulo, Brasil Icon Plc Tempo inteiro

    Job SummaryWe are seeking a highly skilled Clinical Research Associate to join our team at ICON Plc. As a Clinical Research Associate, you will be responsible for managing clinical trials and ensuring compliance with regulatory requirements.Key ResponsibilitiesManage clinical trials from initiation to close-outEnsure compliance with ICH GCP guidelines and...

  • Clinical Research Associate

    2 semanas atrás


    São Paulo, São Paulo, Brasil Novasyte Tempo inteiro

    **Job Overview**As a Clinical Research Associate, you will be responsible for ensuring the proper conduct of clinical trials at assigned sites. This includes performing site monitoring visits, administering protocol training, and evaluating the quality of study site practices.**Key Responsibilities:**Perform site monitoring visits to ensure compliance with...

  • Clinical Research Associate

    3 semanas atrás


    São Paulo, São Paulo, Brasil Novasyte Tempo inteiro

    Job OverviewWe are seeking a highly skilled Clinical Research Associate to join our team. As a Clinical Research Associate, you will be responsible for ensuring that sites are conducting studies and reporting data as required by the study protocol, applicable regulations, and sponsor requirements.Key Responsibilities:Perform site monitoring visits to ensure...


  • São Paulo, São Paulo, Brasil Caidya Tempo inteiro

    Job Title: Clinical Research Associate IIJob Location: HomebasedThis is a part-time, contractor position for up to 0.5 FTE covering sites in Brazil for an oncology study.Job Overview:The Clinical Research Associate II monitors investigational sites to ensure subject safety and provides high-quality data review and reporting in compliance with the Caidya...


  • São Paulo, São Paulo, Brasil Fortrea Tempo inteiro

    Job Overview:Fortrea is seeking a skilled Clinical Research Associate to join our team. As a Clinical Research Associate, you will be responsible for site monitoring and site management for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines.Key Responsibilities:Implement project plans as...


  • São Paulo, São Paulo, Brasil PSI Tempo inteiro

    Job SummaryThe Lead Clinical Research Associate will oversee local Monitors, supervising clinical monitoring and site management activities to ensure the protection of trial subjects' rights, safety, and well-being, data quality, and study compliance on a country/regional level.Key ResponsibilitiesFacilitate regional projects as Lead Monitor and supervise...


  • São Paulo, São Paulo, Brasil Icon Plc Tempo inteiro

    Clinical Research Associate II Specialist at ICON plc is a world-leading healthcare intelligence and clinical research organization.We foster an inclusive environment driving innovation and excellence, and welcome you to contribute to our mission to shape the future of clinical development.We are seeking a Clinical Research Associate II Specialist to join...


  • São Paulo, São Paulo, Brasil Beigene Tempo inteiro

    Job SummaryWe are seeking a highly skilled Clinical Research Associate to join our team at BeiGene. The successful candidate will be responsible for conducting site visits, monitoring data quality, and ensuring compliance with ICH-GCP guidelines and local regulations.Key Responsibilities:Perform and coordinate assigned aspects of the clinical monitoring...

Senior Clinical Research Associate

2 meses atrás


São Paulo, São Paulo, Brasil Icon Plc Tempo inteiro
About ICON Plc

ICON Plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

Our Culture

At ICON, it's our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients' lives.

Our Values

We're driven by four key values that bring us together as individuals and set us apart as an organisation:

  • Accountability & Delivery
  • Collaboration
  • Partnership
  • Integrity

We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development.

The Role

As a Clinical Research Associate at ICON, you'll work within a large-scale, fast-paced environment alongside a close-knit team of highly qualified CRAs to identify, select, initiate and close-out investigational sites for clinical studies in phases II - IV, ensuring adherence to applicable regulations and principles of ICH-GCP.

Key Responsibilities
  • Working independently and actively to coordinate activities to set up and monitor a study, completing accurate study status reports and maintaining study documentation.
  • Submission of protocol, consent documents for ethics/IRB approval and assist in preparing regulatory submissions as requested.
  • Participate in preparing and reviewing study documentation and feasibility studies for new proposals as required.
  • Balancing sponsor generated queries efficiently and responsible for study cost-effectiveness.
  • Dependent on level of experience you may assist in training and mentoring less expert CRA's and/or lead CRA's working on international projects.
Requirements
  • 24 months+ of monitoring experience in phase I-III trials as a CRA.
  • Knowledge of ICH GCP guidelines and expertise to review and evaluate medical data.
  • Excellent written and verbal communication in English.
  • Ability to produce accurate work to tight deadlines within a pressurized environment.
  • Willingness to travel at least 60% of the time.
Benefits

We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals - both ours and yours.

We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans - and related benefits such as life assurance - so you can save and plan with confidence for the years ahead.

But beyond the competitive salaries and comprehensive benefits, you'll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change.

ICON is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.