Clinical Research Associate

hace 11 horas


Ciudad de México, Ciudad de México CDS Fortrea Inc. A tiempo completo
{"title": "Clinical Research Associate", "content": "Job Summary

CDS Fortrea Inc. is seeking a highly skilled Clinical Research Associate to join our team. As a Clinical Research Associate, you will be responsible for monitoring clinical sites, maintaining study files, and conducting pre-study and initiation visits. You will also be responsible for ensuring the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools.

Key Responsibilities
  • Monitor study sites to ensure compliance with protocol and regulatory requirements
  • Maintain accurate and detailed records of site visits and data collection
  • Conduct pre-study and initiation visits to ensure site readiness
  • Ensure the protection of study patients by verifying informed consent procedures and protocol requirements
  • Monitor data for missing or implausible data
Requirements
  • University or college degree, or certification in a related allied health profession
  • Thorough knowledge of ICH Guidelines and local regulatory requirements
  • Strong experience with Clinical Monitoring
  • Ability to work independently and as part of a team
  • Excellent communication and interpersonal skills
About CDS Fortrea Inc.

CDS Fortrea Inc. is a leading global contract research organization with a passion for scientific rigor and decades of clinical development experience. We provide pharmaceutical, biotechnology, and medical device customers with a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas.

", "lang_code": "en-US"}

  • Ciudad de México, Ciudad de México MEX Labcorp Clinical Development, S. de R.L. de C.V. A tiempo completo

    About the RoleMEX Labcorp Clinical Development, S. de R.L. de C.V. is seeking a highly skilled Clinical Research Manager to lead the execution of clinical trials in our region. As a key member of our team, you will be responsible for managing trial operations, ensuring compliance with regulatory requirements, and collaborating with cross-functional teams to...


  • Ciudad de México, Ciudad de México PSI CRO A tiempo completo

    About PSI CROPSI CRO is a leading Contract Research Organization with over 25 years of experience in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering high-quality and on-time services across a variety of therapeutic indications.Job SummaryWe are seeking a highly skilled Clinical...


  • Ciudad de México, Ciudad de México PSI CRO A tiempo completo

    About PSI CROPSI CRO is a leading Contract Research Organization with over 25 years of experience in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering high-quality and on-time services across a variety of therapeutic indications.Job SummaryWe are seeking a highly skilled Clinical...


  • Ciudad de México, Ciudad de México Worldwide Clinical Trials A tiempo completo

    {"title": "Clinical Assessment Technologies Department", "description": "**About the Role**Worldwide Clinical Trials is seeking a skilled Clinician to join our Clinical Assessment Technologies Department. As a Clinician, you will be responsible for all aspects of assigned projects, including clinical assessment, training development, and data review.**Key...


  • Ciudad de México, Ciudad de México IQVIA A tiempo completo

    Job OverviewWe are seeking a highly skilled and experienced Senior Clinical Research Associate to join our team at IQVIA. As a Senior 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...


  • Ciudad de México, Ciudad de México MMATISS A tiempo completo

    Key Responsibilities:Manages clinical investigational sites, ensuring compliance with regulatory requirements and protocol guidelines.Key Accountabilities:Trains and directs investigators and site staff on clinical trial protocols and procedures.Reviews and verifies clinical documentation to ensure accuracy and completeness.Maintains drug accountability and...


  • Ciudad de México, Ciudad de México ICON A tiempo completo

    About the RoleWe are seeking a highly experienced and skilled Senior Clinical Research Associate to join our team at ICON. As a Senior Clinical Research Associate, you will play a key role in the success of our clinical trials by providing expert advice and guidance to less experienced colleagues.Key ResponsibilitiesExpert Advisor: Act as an expert advisor...


  • Ciudad de México, Ciudad de México Worldwide Clinical Trials A tiempo completo

    About the RoleWe are seeking a highly organized and detail-oriented Clinical Operations Associate to join our team at Worldwide Clinical Trials. As a key member of our Clinical Assessment Technologies group, you will play a critical role in ensuring the successful execution of clinical trials.Key ResponsibilitiesTrack and manage rater experience...


  • Ciudad de México, Ciudad de México Novo Nordisk A tiempo completo

    About the Role:The Clinical Research Associate plays a critical role in ensuring the integrity and validity of clinical research data. As a key member of the research team, you will be responsible for managing and supporting clinical research sites, monitoring clinical data to ensure data integrity, scientific validity, and patient safety.Key...


  • Ciudad de México, Ciudad de México Covance Latinoamérica A tiempo completo

    Company Overview:Covance Latinoamérica is a leading global provider of drug development services, dedicated to improving health and advancing medical research.Position Summary:This role presents an exciting opportunity to contribute to the dynamic field of clinical research. As a Clinical Research Assistant, you will play a crucial role in supporting...


  • Ciudad de México, Ciudad de México Covance Latinoamérica A tiempo completo

    Covance Latinoamérica: Clinical Research AssistantWe are seeking a highly motivated and organized Clinical Research Assistant to join our team in Mexico. As a Clinical Research Assistant, you will play a key role in the success of our clinical trials by providing administrative support to our project team and study sites.Key Responsibilities:Act as the...


  • Ciudad de México, Ciudad de México PSI A tiempo completo

    Job OverviewAs a Lead Clinical Research Associate, you will play a key role in managing local Monitors and overseeing clinical monitoring and site management activities to ensure the protection of trial subjects' rights, safety, and well-being, as well as data quality and study compliance on a country/regional level.Key ResponsibilitiesFacilitate regional...


  • Ciudad de México, Ciudad de México IQVIA A tiempo completo

    {"Job OverviewAs a Clinical Research Associate at IQVIA, you will be responsible for ensuring the quality and integrity of study site practices related to the proper conduct of clinical trials. Your primary focus will be on monitoring and site management to ensure that sites are conducting the study(ies) and reporting study data as required by the study...


  • Ciudad de México, Ciudad de México Covance Latinoamérica A tiempo completo

    Company Overview:Covance Latinoamérica is expanding its operations, providing a dynamic opportunity within a rapidly growing sector of our organization.Key Responsibilities:• Serve as the primary liaison for project teams and study sites.• Conduct Case Report Form (CRF) evaluations, generate queries, and resolve discrepancies according to established...


  • Ciudad de México, Ciudad de México Covance Latinoamérica A tiempo completo

    About the RoleCovance Latinoamérica is seeking a highly motivated and detail-oriented Clinical Research Assistant to join our team in Mexico. As a Clinical Research Assistant, you will play a critical role in the success of our clinical trials by providing administrative support to our project teams.Key ResponsibilitiesProject Support: Act as a liaison...


  • Ciudad de México, Ciudad de México Psi CRO Ag A tiempo completo

    About the RoleWe are seeking an experienced Clinical Research Associate to join our team as a Site Lead. As a Site Lead, you will be responsible for conducting and reporting onsite monitoring visits, as well as being involved in study startup and CRF review.This is a home-based position in Mexico, and you will be required to travel. You will be working...


  • Ciudad de México, Ciudad de México IQVIA A tiempo completo

    Job OverviewAs a Clinical Research Associate at IQVIA, you will play a critical role in ensuring the successful execution of clinical trials. Your primary responsibility will be to conduct site monitoring visits to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations, and sponsor...


  • Ciudad de México, Ciudad de México PSI CRO A tiempo completo

    Job OverviewAs a Clinical Research Associate at PSI CRO, you will play a vital role in ensuring the success of clinical studies across various therapeutic indications. Our team is committed to delivering high-quality services, and we are seeking a skilled professional to join our ranks.Key ResponsibilitiesMonitoring and Reporting: Conduct and document onsite...


  • Ciudad de México, Ciudad de México PSI CRO A tiempo completo

    Job SummaryAs a Clinical Research Associate at PSI CRO, you will have the opportunity to work on a variety of monitoring tasks and contribute to clinical studies in different therapeutic indications, maintaining the highest quality standards in the industry. We are committed to developing our employees in their careers by providing tailored courses and...


  • Ciudad de México, Ciudad de México ICON Plc A tiempo completo

    About the RoleWe are seeking a highly experienced and skilled Senior Clinical Research Associate to join our team at ICON Plc. As a Senior Clinical Research Associate, you will play a key role in ensuring the successful delivery of clinical trials by providing expert advice and guidance to less experienced colleagues.Key ResponsibilitiesExpert Advisor: Act...