Clinical Project Coordinator, Biotech

hace 6 días


Ciudad de México, Ciudad de México IQVIA A tiempo completo

IQVIA Biotech is growing Our team in Mexico has openings for Clinical Project Coordinators. This role can be home-based anywhere in Mexico.

Job Overview

Support, with minimal supervision, the Project Leader (PL) and Clinical Project Manager (CPM) with project management activities to ensure all work is conducted in accordance with standard operating procedures (SOPs), policies and practices, good clinical practices (GCP), applicable regulatory requirements, and meets quality/timeline metrics. Ensure customer satisfaction is met in relation to assigned project/s.

Essential Functions

  • Assist in the establishment and maintenance of all project documentation including all files, records and reports according to the scope of work and standard operating procedures (SOPs).
  • Assist with periodic review/audit of files for accuracy and completeness.
  • Assist with the coordination and tracking of all information, communications, documents, materials, and supplies for assigned projects.
  • Manage study specific eTraining and oversee compliance.
  • Support the updating and maintenance of internal systems, databases, tracking tools, timelines and project plans with project specific information.
  • Prepare and distribute status, tracking and project finance reports, and assist the project manager(s) with budget allocation and approval of invoices.
  • Organize and support project leader (PL) in managing internal study team and customer meetings.
  • Take and record minutes, notes and actions at assigned meetings, distribute and follow up accordingly.
  • Support the preparation of presentation materials for meetings (internal/external) and project summary data.
  • Support the coordination of project team and/or customer meetings including logistics and materials required.
  • Identify and escalate discrepancies in project tracking data, timesheet coding, expense data billing etc.
  • Establish and manage performance dashboards, analyze event triggers and alerts and determine appropriate follow up for PL or others to act upon.
  • Monitor metrics and make required updates in IQVIA systems to ensure accurate and timely reporting is available to senior management.
  • Assist in the establishment and maintenance of all project documentation including all files, records and reports according to the scope of work and SOPs.
  • Coordinate onboarding of new Key Members and system access.
  • Assist in the training and orienting of more junior project support staff.

Qualifications

  • Bachelor's Degree Bachelor's Degree in life sciences or other related field required Req
  • Typically requires 2-3 or more years of experience.
  • Requires good knowledge within a specific discipline typically gained through extensive work experience and/or education.
  • 4 – 5 years' experience or equivalent combination of education, training, and experience.
  • Knowledge of clinical trials - basic knowledge of applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.;
  • Communication - strong written and verbal communication skills including good command of English language. Good communication and interpersonal skills.
  • Problem solving - good problem solving skills.
  • Quality - results and detail-oriented approach to work delivery and output. Good planning, time management, and prioritization skills. Attention to detail and accuracy in work.
  • IT skills - good software and computer skills, including MS Office applications.
  • Collaboration - ability to establish and maintain effective working relationships with coworkers, managers, and clients.
  • Cross-collaboration - ability to work across geographies displaying high awareness and understanding of cultural differences.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide . Learn more



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

    IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile, therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to patients faster.IQVIA Biotech is seeking an experienced Clinical Project Manager based in Mexico to lead and deliver innovative...


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

    IQVIA Biotech is growing Our team in Mexico has openings for Clinical Project Coordinators. This role can be home-based anywhere in Mexico.Job OverviewSupport, with minimal supervision, the Project Leader (PL) and Clinical Project Manager (CPM) with project management activities to ensure all work is conducted in accordance with standard operating procedures...


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

    IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile, therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to patients faster. IQVIA Biotech is seeking an Associate Clinical Project Manager based in Mexico with experience in Immuno-oncology...


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

    Clinical Process Coordinator, cFSPHybrid role (Mexico City)Job OverviewLeads and oversees the execution of clinical projects and research studiesProvide project related assistance for all assigned project(s), sites and project teams. Ensure all work is conducted in accordance with SOPs, policies and practices, in accordance with global and local regulations...

  • Assoc Clinical Lead

    hace 4 días


    Ciudad de México, Ciudad de México IQVIA A tiempo completo

    Job OverviewAssociate Clinical Leads are an integral part of clinical trial delivery, working alongside clinical teams to improve patients' lives by bringing new drugs to the market faster. The Associate Clinical Lead is a member of the core project team responsible for clinical delivery of clinical studies to meet contractual requirements in accordance with...

  • Clinical Start-Up

    hace 2 semanas


    Ciudad de México, Ciudad de México Fortrea A tiempo completo

    Position SummaryThe Clinical Start-Up & Trial Lead (Start-Up + CTL) is responsible for the strategic planning, coordination, and oversight of clinical trial start-up activities as well as the ongoing execution of clinical studies. This hybrid role ensures operational excellence from site initiation through to study close-out, serving as the primary...


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

    CDC II - Mexico CityICON 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 developmentClinical Data Coordinator IIThis is a hybrid role requiring 3 days in the office...

  • Project Coordinator

    hace 2 semanas


    Ciudad de México, Ciudad de México Argano A tiempo completo

    Job SummaryJOB DESCRIPTIONWe are seeking an experienced Project Coordinator to join our team. The Project Coordinator will be responsible for coordinating project activities, ensuring that projects are completed on time, within budget, and to the satisfaction of stakeholders. This role requires a strong understanding of project management methodologies,...


  • Ciudad de México, Ciudad de México Medpace, Inc. A tiempo completo

    Our Latin American activities are growing rapidly, and we are currently seeking a full-time, office-based Clinical Safety Coordinator to join our team This position plays a key role in the pharmacovigilance process at Medpace. Working in a team to accomplish tasks and projects that are instrumental to the company's success. If you want an exciting...


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

    Our Latin American activities are growing rapidly, and we are currently seeking a full-time, office-basedClinical Safety Coordinatorto join our team This position plays a key role in the pharmacovigilance process at Medpace. Working in a team to accomplish tasks and projects that are instrumental to the company's success. If you want an exciting career where...