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Central Monitoring Manager - Remote

Posted 9 weeks ago
All others
Full Time
Worldwide

Overview

The Central Monitoring Manager will lead the implementation of risk-based monitoring approaches in clinical studies to ensure patient safety and data integrity.

In Short

  • Lead and facilitate initial and ongoing study Risk Management
  • Participate in selection and setup of the RBM platform
  • Perform Centralized Monitoring including review of Key Risk Indicators
  • Present analysis results to study teams and clients
  • Develop and review study-specific Plans
  • Manage targeted SDV and monitoring strategy
  • Set up and manage Central Data Review activities
  • Contribute to Proposals and bid defense meetings
  • Communicate study challenges to Clinical Data Science group

Requirements

  • College/University degree or equivalent experience
  • Clinical Study Lead/Manager experience
  • Strong communication & presentation skills
  • Leadership and ability to work independently
  • Centralized Monitoring experience is a plus
  • Critical thinking and analytical skills
  • Ability to work with complex data
  • Knowledge of clinical trials processes
  • Full working proficiency in English
  • Proficiency in MS Office applications

Benefits

  • Opportunity to work on the frontline of the industry
  • Set the grounds for risk-based models
  • Gain a global helicopter view on each project
PSI CRO logo

PSI CRO

PSI CRO is a prominent Contract Research Organization (CRO) with over 25 years of experience in the pharmaceutical industry. Founded in Switzerland, PSI is a privately owned, full-service CRO that operates globally, supporting clinical trials across various countries and continents. The company is known for its selective approach to project engagement, emphasizing high-quality and timely services across a wide range of therapeutic areas. PSI values diversity and inclusivity within its workforce, fostering an environment where all colleagues feel welcomed and valued. The organization is dedicated to not only conducting clinical trials but also building a community that empowers team members to thrive and contribute to significant advancements in the pharmaceutical sector.

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