Clinical Research Associate II

2 semanas atrás


São Paulo, São Paulo, Brasil Allergan Tempo inteiro

Job Summary

As a Clinical Research Associate II at AbbVie, you will play a critical role in the successful execution of clinical studies. Your primary responsibility will be to monitor the activities conducted by clinical investigative sites, ensuring adherence to federal regulations, Good Clinical Practices (GCPs), and AbbVie Standard Operating Procedures (SOPs).

Key Responsibilities

• Conduct site qualification, initiation, interim monitoring, and study close-out visits for Phase 1-4 studies in accordance with applicable regulations, GCPs, and AbbVie SOPs.

• Monitor and manage the site's overall activities, motivating and influencing site personnel to meet study objectives.

• Identify and evaluate new potential investigators/sites, recommending them for future studies.

Requirements

• Tertiary qualification, health-related (e.g., Medical, Scientific, Nursing) preferred.

• Minimum 1 year of clinically-related experience, with 6 months in clinical research monitoring.

• Current in-depth knowledge and understanding of appropriate therapeutic indications and clinical trial regulations.

• Strong planning and organizational skills, with the ability to work in a dynamic environment with competing projects and deadlines.



  • 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 Title: Clinical Research Associate IIWe are seeking a highly motivated and experienced Clinical Research Associate II to join our team at BeiGene. As a Clinical Research Associate II, you will be responsible for conducting site visits, monitoring data quality, and ensuring patient safety in accordance with ICH-GCP guidelines and local regulations.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...

  • Clinical Research Associate

    4 semanas 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 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

    4 semanas 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...


  • 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

    4 semanas atrás


    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 CTI Clinical Trial Services, Inc Tempo inteiro

    Principal Clinical Research AssociateJob SummaryCTI Clinical Trial Services, Inc. is seeking a highly skilled and experienced Principal Clinical Research Associate to join our team. As a key member of our clinical operations team, you will be responsible for overseeing the management of clinical trials, ensuring compliance with regulatory requirements, and...


  • 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...


  • São Paulo, São Paulo, Brasil ICON Tempo inteiro

    About the RoleWe are seeking a highly skilled Clinical Research Associate to join our team at ICON. 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 ResponsibilitiesConduct on-site and remote monitoring activities to ensure...

  • Clinical Research Associate

    4 semanas atrás


    São Paulo, São Paulo, Brasil Novasyte Tempo inteiro

    **Job Overview**As a Clinical Research Associate at Novasyte, you will be responsible for ensuring the quality and integrity of study site practices related to the proper conduct of clinical trials. This includes performing site monitoring visits, administering protocol and related study training, and evaluating the quality of study site practices.**Key...

  • Clinical Research Associate

    4 semanas atrás


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

    **Clinical Operations Role**At Thermo Fisher Scientific, we're committed to enabling our customers to make the world healthier, cleaner, and safer. As a Clinical Research Associate, you'll play a crucial part in bringing our Mission to life by providing end-to-end support for clinical trials from study start-up to monitoring through to study close-out.**Key...

  • Clinical Research Associate

    4 semanas atrás


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

    Job SummaryWe are seeking a highly skilled Clinical Research Associate (CRA) - Level II to join our team at Thermo Fisher Scientific. As a CRA, you will be responsible for monitoring investigator sites to ensure compliance with regulatory requirements and Good Clinical Practice (GCP) guidelines.Key ResponsibilitiesMonitor investigator sites with a risk-based...

  • Clinical Research Associate

    2 semanas atrás


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

    Job SummaryThermo Fisher Scientific is seeking a skilled Clinical Research Associate to join our team. The successful candidate will be responsible for monitoring investigator sites with a risk-based approach, ensuring data accuracy, and conducting site initiation and close-out activities. This role is ideal for a detail-oriented professional with experience...

  • Clinical Research Associate

    4 semanas atrás


    São Paulo, São Paulo, Brasil PSI CRO Tempo inteiro

    Company OverviewPSI CRO is a leading Contract Research Organization with a strong presence in the industry, offering a perfect balance between stability and innovation to both clients and employees.Job ResponsibilitiesAs a Medical Monitor at PSI CRO, you will provide medical input to global clinical studies and advise the teams and business partners,...


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

    About the RoleWe're seeking a highly skilled Clinical Research Associate to join our team at ICON Plc.Key Responsibilities:Identify, select, initiate and close-out investigational sites for clinical studies in phases II - IV.Ensure adherence to applicable regulations and principles of ICH-GCP.Work within a large-scale, fast-paced environment alongside a...


  • São Paulo, São Paulo, Brasil Milestone One Tempo inteiro

    At Milestone One, we're on a mission to support clinical study sites in delivering stronger studies. To achieve this goal, we're seeking an experienced Senior Clinical Research Associate to join our team.About the RoleWe're looking for a highly skilled SCRA professional to find and build relationships with new clinical trial sites, actively promoting our...

  • Clinical Research Associate

    2 semanas atrás


    São Paulo, São Paulo, Brasil Lilly Tempo inteiro

    At Lilly, we are committed to making life better for people around the world. Our team of professionals works to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. To achieve this mission, we need a skilled Clinical...


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

    Clinical Research Excellence at CTI Clinical Trial Services, IncWe maintain a culture of excellence across all regions by ensuring our remote employees are fully engaged. To achieve this, we hold weekly all-staff meetings. Each department provides an update on their study or milestone progress. Additionally, our employees can participate in one of our CTI...