Clinical Research Manager

hace 3 días


Santiago, Metropolitana, Chile ICON A tiempo completo
Job Description

As a Clinical Trial Manager at ICON, you will be part of the world's largest and most comprehensive clinical research organization. Your role will involve joining a solid partnership and an environment driven by innovation and continuous improvement.

You will have the opportunity to work in an environment where people feel they belong and are empowered to reach their full potential, perform at their best, and make a valued contribution to saving lives.

  • Key Responsibilities:
  • Planning, management, and oversight of clinical study execution in accordance with the global program strategy, through leadership of the cross-functional Local Study Team (LST).
  • Contribution and development of program/study-specific materials – e.g., monitoring plan, study specific training documents.
  • Accountability for site-level goal setting and study-specific deliverables for clinical sites within your country/-ies.
  • Contribution to, delivery, and/or lead CRA, Investigator, and Study Coordinator training.
  • Oversight and monitoring of applicable vendor activities – e.g., laboratories and equipment provisioning.
  • Country-level input into the Country Operational Plan (COP) and partnership with the DFM through feasibility and with the GCMs to ensure local delivery of the study.
  • Responsibility for approval of Baseline and Revised Enrolment Plans (Country Level).
  • Monitoring of the execution of the clinical study against timelines, deliverables, and budget for that country.
  • Translation of global start-up requirements into local country targets.
  • Monitoring and acting upon data flow metrics – review, trend identification, and analysis, with targeted follow-up where appropriate.
  • Identification and facilitation of resolution of cross-functional study-specific issues.
  • Escalation of any issues related to delivery, timelines, or budget to GCMs (or TMT lead if appropriate).
  • Execution of regulatory agency inspection readiness activities – e.g., TMF review, story board generation.
  • Collaboration with local teams to ensure country-level study delivery is aligned with global expectations.
  • Identification of risk, implementation of risk mitigation strategies, and resolution of issues at a country/site level, as well as informing the CST/TMT, LST, and local teams of risks associated with delivery in a proactive, timely, and solution-oriented manner.

About You

  • Bachelor's degree in a health, life sciences, or other relevant field of study.
  • Minimum 5-6 years' work experience in clinical research or knowledge in Project Management and Site Management.
  • CRA Experience preferred.


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