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Clinical Research Project Coordinator

hace 1 semana


Xico, México Icon Plc A tiempo completo

Company Overview

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At ICON, we are a world-leading healthcare intelligence and clinical research organization. Our mission is to shape the future of clinical development, and we're proud to foster an inclusive environment driving innovation and excellence.

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Job Summary

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We are seeking a highly motivated Clinical Research Project Coordinator to join our team in Mexico City. This is a challenging role that requires strong organizational skills, attention to detail, and excellent communication abilities.

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Key Responsibilities:

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  • ">
  • Manage projects in a timely manner in adherence with ICON's SOPs, ICH, GCP, and appropriate regulations">
  • Delivery of projects in accordance with the contract, timelines, and study budget">
  • Identification and review of change orders for the budget">
  • Attend and present at client investigator, kick-off, and client meetings">
  • Ensure all necessary study-specific training is provided to the study team to improve performance and knowledge">
  • Management of eCRF development process">
  • Development/Review/Maintenance of all trial documentation (Charter, eCRF, SRS, Reviewer Training Manuals)">
  • User Acceptance Training and demonstration of eCRF">
  • Data reconciliation">
  • Primary client and CRO contact; develops successful working relationships with client/CRO">
  • Preparation and management of meeting agendas and minutes">
  • Prepare/Approve Project Reports">
  • Management of Study Centers">
  • Coordinates readers and review sessions">
  • Conducts reader training with support of Project Director">
  • Monitors Offsite Assessments/Blinded Reads">
  • Quality Control of Offsite Assessments/Blinded Reads">
  • Ensures all management/tracking systems are up-to-date">
  • Provide regular feedback to senior management on project status, client satisfaction, and staffing issues">
  • Manages Data Management Lead for scheduling and preparation of data deliveries as required">
  • Participate in BD activities as appropriate">
  • Supports internal, client, and regulatory audits">
  • Ability and willingness to travel">
  • Participate in interviews as required">
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Requirements:

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To be considered for this role, you will need to have a minimum of a bachelor's degree (preference in Life Sciences or similar) or equivalent education/work experience.

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You should also have relevant work experience in timeline management and previous experience in a project management role within the clinical trial industry.

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Advanced English fluency is required for business communication.

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What We Offer:

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We offer very competitive salary packages, including an estimated annual salary of $120,000 - $150,000 depending on experience.

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In addition to a competitive salary, we provide a range of health-related benefits to employees and their families, including comprehensive health insurance and retirement plans.

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We also offer opportunities for professional growth and development, as well as a dynamic and supportive work environment.

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Equal Opportunities Employer:

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ICON is an equal opportunity and inclusive employer committed to providing a workplace free of discrimination and harassment.