Central Monitoring Manager

PSI CRO AG

. Lead and facilitate initial and ongoing study Risk Management .

Posted 9/15/2026full-timeRemote • LithuaniaMid-LevelSenior💰 €77,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in Risk Management and Centralized Monitoring within clinical trials, with strong analytical skills to interpret complex data and provide actionable insights. Proficient in developing study-specific plans and communicating effectively with cross-functional teams and clients.

Highest-signal resume keywords

Clinical Study Lead/Manager ExperienceRisk ManagementCentralized MonitoringStrong Communication SkillsProficiency in MS Office Applications

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Risk ManagementCentralized MonitoringStatistical AnalysisData ReviewExcel Skills

Soft Skills

LeadershipCritical ThinkingAnalytical SkillsAdaptabilityPresentation Skills

Industry Keywords

Clinical TrialsRisk Based MonitoringKey Risk IndicatorsQuality Tolerance LimitsStudy Protocol

About the role

Key responsibilities & impact

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
Manage issues in a 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 the Clinical Data Science group and work out data-driven solutions

Requirements

What you’ll need

College/University degree or an equivalent combination of education, training and experience
Clinical Study Lead/Manager experience
Strong communication and presentation skills
Leadership and ability to work independently
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; Lithuanian proficiency is a plus
Proficiency in MS Office applications
Excel skills

Benefits

Comp & perks

Excellent working conditions
Extensive training
Friendly team
Opportunities for personal and professional growth
Fair and attractive salary and benefits package