Ceva Clinical Reviewer

hace 2 semanas


Desde casa, México IQVIA A tiempo completo

**Job Overview**In-depth knowledge of applicable global, regional and local clinical research regulatory requirement; i.e. Good Clinical Practice (GCP) and International. Provide departmental support to Clinical Event Validation and Adjudication (CEVA) Management and project support to CEVA Project Managers/Leads. Support provided is typically broad in scope and complex. Support leadership and accountability for all aspects of assigned CEVA projects, working cross-functionally and across the opportunity lifecycle, integrating delivery into one seamless and transparent program for customers in areas of event adjudication in accordance with Standard Operating Procedures (SOPs), policies and practices.**Essential Functions**- Assist the CEVA lead in the identification of source documents needed by the Endpoints Adjudication Committee (EAC) for the trial endpoints as indicated by the needs of the project with mínimal guidance of Senior specialist.- Assist the CEVA lead on the clinical aspects of project processes in the development of documents, forms, and workflows as indicated by the project.- Assist the CEVA lead to manage realization/profitability and revenue recognition for assigned projects. Responsible for updating financial systems, invoicing, project budget review, project financial analysis, pursuit of change orders if required.- Collaborate with CEVA team members to achieve departmental goals i.e. understand quality requirements and assist in the achievement of productivity, utilization, and realization metrics.- Manage the processing of CEVA data by collecting and tracking incoming data, determining initial/update status of incoming data (endpoints, etc.) and distributing event information to appropriate project personnel in the workflow for continued processing.;- Provide clinical judgment during the review of documents to determine if the existing information is sufficient for the reported clinical endpoint to be adjudicated as per work assignment.- Work closely with internal and / or external partners to manage development, testing, and use of electronic systems necessary for CEVA project processes.- Develop and provide project-specific CEVA process training to CEVA team members, monitors, and investigative site personnel, as appropriate.- Attend meetings with internal and external stakeholders. Provide project status updates, support processes, and project planning/strategy. Provide feedback to CEVA Management/ Line manager on any challenges/issues and successes.;**Qualifications**- Bachelor's Degree Nursing Degree or Bachelor's degree in life sciences or educational equivalent in health science or other directly related field and clinical trial knowledge; or equivalent combination of education, training, or experience.- Equivalent combination of education, training, or experience- Strong prioritization (critical timelines), planning and organizational skills.- Effective verbal and written communication skills including ability to work and lead teleconferences.- Effective collaborative, organizational and delegation skills.- Independently work on multiple projects and manage competing priorities.**#LI-Remote****#LI-MARIAARECHAGA



  • Desde casa, México IQVIA A tiempo completo

    Job OverviewProvide management and service delivery excellence of (Clinical Event Validation and Adjudication) CEVA, OGM (Oversight Group Management) projects, as assigned by CEVA Management, covering single or multiple CEVA-OGM functions, with supervision from project oversight. Provide administrative coordination for Oversight Groups (Data Monitoring...


  • Desde casa, México IQVIA A tiempo completo

    Job Overview Provide management and service delivery excellence of (Clinical Event Validation and Adjudication) CEVA, OGM (Oversight Group Management) projects, as assigned by CEVA Management, covering single or multiple CEVA-OGM functions, with supervision from project oversight. Provide administrative coordination for Oversight Groups (Data Monitoring...

  • Medical Data Reviewer

    hace 5 días


    Desde casa, México ICON A tiempo completo

    ICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organizations.With our patients at the center of all that we do, we help to accelerate the development...

  • Medical Data Reviewer

    hace 7 días


    Desde casa, México ICON A tiempo completo

    ICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organizations. With our patients at the center of all that we do, we help to accelerate the development...


  • Desde casa, México Signant Health A tiempo completo

    **Job Details**:- ** Position**:Psychiatric/Cognitive Scales Quality Reviewer - Science & Medicine- (This is a remote role located in Mexico)**Are you ready for the Most Impactful Work of Your Life?**Working at Signant Health puts you at the very heart of the world’s most exciting sector - a high-growth, dynamic company in an extraordinary industry....


  • Desde casa, México IBI Healthcare Institute A tiempo completo

    Key Responsibilities:- Review and evaluate preauthorization requests for medical procedures within a large surgical center.- Ensure that all preauthorization documentation is complete, accurate, and in compliance with established medical guidelines and protocols.- Collaborate with healthcare providers, physicians, and other stakeholders to obtain additional...


  • Desde casa, México IQVIA A tiempo completo

    **POSITION TITLE**: Lead Clinical Data Manager**REPORTS TO**: Manager or Director level Data Management or Designee**BASIC FUNCTIONS**:Lead Clinical Data Manager position is to manage all data management (DM) tasks for multiple projects from project start-up through database closure and archival producing high-quality databases for analysis and potential...


  • Desde casa, México IQVIA A tiempo completo

    **POSITION TITLE**: Principal Data Manager**REPORTS TO**: Manager or Director level Data Management or Designee**BASIC FUNCTIONS**:Principal Data Manager position is to manage all data management (DM) activities for more complex, larger projects and/or program of studies from start-up through database closure and archival, producing high quality databases...

  • Medical Record Reviewer

    hace 1 semana


    Desde casa, México BW A tiempo completo

    You will review summaries (and do quality control) of medical records broken down by different visits, and compare the results with the original source documents. Correct the AI summary of any inconsistencies to match the original document, and other formatting or re-summarizing changes that need to be made. Bonus points if you are a nurse or doctor with...

  • Clinical Rater

    hace 1 semana


    Desde casa, México Signant Health A tiempo completo

    (This is a remote role located in Mexico) **Are you ready for the Most Impactful Work of Your Life?** Working at Signant Health puts you at the very heart of the world’s most exciting sector - a high-growth, dynamic company in an extraordinary industry. We’re radically changing the clinical trial landscape, driving change through the technology and...