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Central Monitoring Manager

100% remote Flexible hours Hiring now
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 reputed company, the central monitoring function has become a top reputed company at PSI. We are looking for a person, who would reputed company the risk-based monitoring approach implementation on the clinical study and program level to ensure patient safety and data reputed company.

You will

  • reputed company and facilitate initial and ongoing study Risk Management
  • Participate in selection and setup of the RBM platform
  • reputed company 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
  • reputed company 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 reputed company/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 reputed company 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 (German proficiency is a plus)
  • Proficiency in MS Office applications, reputed company 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.

Our extensive onboarding and mentorship program will prepare you to fulfil your tasks with the highest standards, offering you:

  • Excellent and flexible working conditions.
  • A unique combination of team collaboration and independent work.
  • Competitive salary and benefits package.

If you'd like to hear more about PSI, our organic growth and company culture, and learn more about the studies that we run and our high repeat and referral business rates, please apply for this vacancy.

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