Clinical Research Associate II - Brazil - ICON Strategic Solutions

    ICON Strategic Solutions
    ICON Strategic Solutions Brazil

    há 1 semana

    Default job background
    Farmacêutico / Bio-tech
    Descrição

    A Clinical Research Associate is a professional who contributes to accelerated drug/device/outcomes research through independent monitoring of studies to ensure patient safety and data integrity.

    You will be joining a program that takes an extensive co-monitoring approach, enabling a supportive and collaborative work environment. Frequent, consistent communication, both internally and with our client, positions our program to be closely aligned on our shared goals.

    The Clinical Research Associate monitors the progress of clinical studies at investigative sites or remotely, ensuring clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), International Conference on Harmonization Good Clinical Practices (ICH-GCP) and all applicable regulatory requirements.

    • Completes onsite and remote monitoring activities in accordance with all ICH-GCP guidelines, applicable regulations, SOPs and study processes. Activities include qualifying potential investigative sites, initiating clinical trials, maintaining study files, providing instructions to site personnel and study close out.
    • Verifies the protection of study participants by confirming informed consent procedures and protocol have been performed in accordance with applicable regulations.
    • Ensures the integrity of clinical data and that the study is conducted in compliance with approved protocol, GCP, applicable regulations and SOPs.
    • Manages the investigative site staff to facilitate trial deliverables, e.g., subject enrollment, data deliverables.
    • Verifies proper management and accountability of Investigational Product (IP).
    • Manages essential documents as required by local regulations and ICH-GCP guidelines before, during and after a clinical study; assists with resolution of investigational site/data queries.
    • Performs key risk assessment and management responsibilities throughout the project, including key risk indicator and site health analysis, site process evaluation, and project escalation.
    • Participates in audit preparation and follow-up activities as needed.
    • Independently performs a variety of onsite and offsite monitoring visit types.
    • Gathers and reviews information for assigned site and identifies inconsistencies. With limited guidance from project and functional management, assesses risk and escalates as appropriate.
    • Assists with non-complex ad-hoc, short-term assignments in support of additional studies or departmental initiatives.
    • May serve as preceptor, providing training to less experienced clinical team members.

    Requirements

    • Undergraduate degree or international equivalent in clinical, science, or healthcare-related field from an accredited institution; healthcare professional licensure, i.e., registered nurse.
    • Previous experience supporting clinical trials including solid on-site monitoring experience.
    • Travel is required 50-80%.
    • Equivalent combination of education, training, and relevant experience may be considered in place of the education and experience stated above. All employees must read, write and speak fluent English and host country language.

    What ICON Can Offer You

    Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.

    In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work-life balance opportunities for you and your family.

    At ICON, diversity, inclusion & belonging are fundamental to our culture and values. Our rich diversity makes us more innovative, which helps us better serve our people, patients, customers, and our communities. We're proud of our diverse workforce and the work we've done to become a more inclusive organisation. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON 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.



  • ENGINEERINGUK Brasília

    Job Description · A Clinical Research Associate plays a crucial role in accelerating drug/device/outcomes research by independently monitoring studies to ensure patient safety and data integrity. · The program employs an extensive co-monitoring approach, fostering a supportive an ...


  • ENGINEERINGUK Brasília

    Clinical Research Associate · We are seeking a Clinical Research Associate (CRA) to join our team at ICON. · About the Role: · The successful candidate will contribute to accelerated drug/device/outcomes research through independent monitoring of studies, ensuring patient safety ...


  • ICON Brazil

    Clinical Research Associate Role · A Clinical Research Associate is a professional who contributes to accelerated drug/device/outcomes research through independent monitoring of studies to ensure patient safety and data integrity. · This role involves joining a program that takes ...


  • Parexel Brasília

    Job Description · We are seeking an experienced Clinical Research Associate (CRA) to perform on-site monitoring visits in Brazil. · Oncology experience is required. · Key Responsibilities: · Conduct qualification visits, site initiation visits, monitoring visits, and termination ...


  • ENGINEERINGUK Brazil

    A Clinical Research Associate is a professional who ensures the integrity of clinical trials through independent monitoring and site management. · This role contributes to accelerated drug/device/outcomes research by verifying patient safety, data accuracy, and compliance with re ...


  • ICON Brazil

    A Clinical Research Associate is a professional who plays a pivotal role in accelerating drug/device/outcomes research by independently monitoring studies to ensure patient safety and data integrity. · You will be part of a program that takes an extensive co-monitoring approach, ...


  • Alimentiv Inc Brazil

    Manage, deliver and/or perform full clinical site monitoring services for one or more projects which may include multiple services that are complex in nature and/or run on a multinational scale. This role is based at our office and is responsible for the design and oversight of p ...


  • ICON Brasília

    Job Description · A Clinical Research Associate plays a vital role in accelerating drug/device/outcomes research by independently monitoring studies to ensure patient safety and data integrity. · Key Responsibilities · Conduct onsite and remote monitoring activities according to ...


  • ENGINEERINGUK Brasília

    Clinical Research Associate Job Description · A Clinical Research Associate is a professional who plays a crucial role in accelerating drug/device/outcomes research by conducting independent monitoring of studies to ensure patient safety and data integrity. · You will be part of ...


  • CTI Clinical Trial and Consulting Services Brasília

    Senior Clinical Research Associate - SR CRA · This role is responsible for serving as the main CTI contact for assigned study sites, conducting site visits, and completing site visit deliverables with quality and within given timelines. · About the Role · Assist with study start- ...


  • CTI Clinical Trial and Consulting Services Brazil

    Job Title: Senior Clinical Research Associate · Location: São Paulo, Brazil · Job Type: Full-time · Salary: R$ 8,000 - R$ 12,000 per month · We are seeking a highly skilled and experienced Senior Clinical Research Associate to join our team in São Paulo, Brazil. As a Senior CRA, ...


  • Icon Brasília

    Job Title: Clinical Research Associate · A professional who plays a crucial role in accelerating drug/device/outcomes research by ensuring patient safety and data integrity through independent study monitoring. · Key Responsibilities: · Completes onsite and remote monitoring acti ...


  • MPOWIR Mentoring Physical Oceanography Women to Increase Retention Federative Republic Of Brazil

    Senior Research Associate in Physical Oceanography · We are seeking a highly motivated Senior Research Associate to join our team at the University of East Anglia, working on the NSF-NERC-funded TARSAN project. As a key member of our research group, you will undertake research in ...

  • ENGINEERINGUK

    CRA I or II

    há 6 horas


    ENGINEERINGUK Brasília

    A Clinical Research Associate Role · Clinical Research Associates play a crucial role in accelerating drug/device/outcomes research by independently monitoring studies to ensure patient safety and data integrity. · Key Responsibilities · Perform onsite and remote monitoring activ ...


  • Articul8 AI Brazil

    About us: · We relentlessly pursue excellence and create exceptional AI products that exceed customer expectations. We are a team of dedicated individuals who take pride in our work and strive for greatness in every aspect of our business. · Job Description: · We are seeking an e ...


  • Elsevier Brazil

    We are seeking a highly motivated and experienced Associate Scientific Editor to support researchers in scholarly publication. As part of our Author Heroes team, you will use your PhD and expertise as an author to improve the editorial process and help authors find a suitable hom ...


  • Parexel Brasília

    Clinical Operations Specialist · Join a team of changemakers at Parexel, helping to advance healthcare globally, with the patient at the forefront of our work. · About Us · Parexel is a leading Clinical Research Organization (CRO) specializing in delivering life-changing medicine ...


  • Articul8 AI Brazil

    About Us · We strive for excellence in AI products and services, driven by a team of dedicated professionals who are passionate about innovation. · Job Description: · We are seeking an exceptional Principal AI Researcher to lead the development of novel algorithms and models for ...


  • World Food Programme Brasília

    Procurement Associate · The Centre is an innovation that seeks to respond government demands for technical support to strengthen their national capacities and knowledge on sustainable school feeding and to support them in the design and management of healthy and sustainable natio ...


  • ENGINEERINGUK Brazil

    Global Logistics Associate - Import/Export · The Global Logistics Associate performs investigative site recruitment, clinical status tracking, and in-house site management activities in accordance with the Sponsor and/or PRA protocol, standard operating procedures (SOPs), ICH/GCP ...


  • United Nations Development Programme Brazil

    Job Title: Programme Associate, Women's Economic Empowerment · Description: · The UN Women Country Office in Brazil focuses on three key areas: · Women lead, participate in, and benefit equally from governance systems. · Women have income security, decent work, and economic auton ...

Empregos
>
Clinical research associate ii