Central Monitoring Manager

Remote: 
Full Remote
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Offer summary

Qualifications:

College/University degree or equivalent experience, Clinical Study Lead/Manager experience, Strong communication and presentation skills, Critical thinking and analytical skills.

Key responsibilities:

  • Lead and facilitate study Risk Management
  • Perform Centralized Monitoring and review Key Risk Indicators
  • Present analysis results to study teams and clients
  • Set up and manage Central Data Review activities in a study

PSI CRO AG  logo
PSI CRO AG Pharmaceuticals Large http://www.psi-cro.com
1001 - 5000 Employees
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Job description

Company Description

PSI is a leading Contract Research Organization with almost 30 years on the market, offering a perfect balance between stability and innovation to both clients and employees.  We focus on delivering quality and on-time services across a variety of therapeutic indications.

    Job Description

    With the industry moving forward, the central monitoring function has become a top priority at PSI. We are looking for a person, who would lead the risk-based monitoring approach implementation on the clinical study and program level to ensure patient safety and data integrity.

    You will:

    • Lead and facilitate initial and ongoing study Risk Management
    • Participate in selection and setup of the RBM platform
    • Perform Centralized Monitoring for a study including review of Key Risk Indicators, Statistical Analyses and Quality Tolerance Limits
    • Present Centralized Monitoring analysis results to study teams and clients and manage issues in cross-functional environment
    • Develop and review study-specific Plans
    • Set up and manage targeted SDV and monitoring strategy for a study
    • Set up and manage Central Data Review activities in a study
    • Contribute to Proposals and bid defense meetings with information about Risk Based Monitoring services
    • Communicate study challenges to Clinical Data Science group and work out data-driven solutions

    Qualifications
    • College/University degree or an equivalent combination of education, training and experience
    • Clinical Study Lead/Manager experience
    • Strong communication & presentation skills are essential
    • Leadership and ability to work independently are essential
    • Centralized Monitoring experience is a plus
    • Critical thinking and analytical skills
    • Ability to work with complex data and provide insight into risk reports and trends
    • Ability to adapt to changing circumstances and learn quickly
    • Knowledge of the process and functions in clinical trials, ability to understand the protocol and study associated risks
    • Full working proficiency in English (Polish proficiency is a plus)
    • Proficiency in MS Office applications, Excel skills

    Additional Information

    This role is not only important for every CRO, but it is booming now. This is an opportunity to work on a frontline of the industry, set the grounds for risk-based models and get a global helicopter view on each project.

    Required profile

    Experience

    Industry :
    Pharmaceuticals
    Spoken language(s):
    English
    Check out the description to know which languages are mandatory.

    Other Skills

    • Critical Thinking
    • Leadership
    • Communication
    • Microsoft Excel
    • Microsoft Office
    • Adaptability
    • Analytical Skills

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