Manager, Central Monitoring – Senior Central Monitoring Associate

Parexel

Central Monitoring Manager overseeing clinical trial monitoring and data analysis at Parexel. Leading teams to ensure compliance and quality in global clinical studies.

Posted 4/16/2026full-timeRemote • 🇬🇧 United KingdomSeniorWebsite

About the role

Key responsibilities & impact

Accountable for centralized monitoring activities for global and/or complex trials
Analytical data review of key risk and/or operational performance data
Present findings as an integral member of the Clinical Study team
Collaborate on Study Quality Risk Assessment
Lead the creation of the Central Monitoring Plan
Work with data analysts to configure, implement, and execute the Central Monitoring RBQM system
Conduct study-level Central Monitoring Reviews

Requirements

What you’ll need

At least 7 years of relevant experience in the biotechnology/pharmaceutical industry
Minimum of 1 year with direct Central Monitoring experience
Site monitoring or data management experience essential
Experience using CluePoints is essential
Excellent written communication skills
Aptitude for mathematical concepts
Knowledge and experience with clinical databases, electronic data capture systems, quality control processes, and auditing procedures

Benefits

Comp & perks

Fully remote home-based position
Collaborate on Study Quality Risk Assessment
Develop and Author the Central Monitoring Plan
Oversee Central Monitoring Execution
Analyze and Interpret Data Trends
Facilitate Study Team Decisions
Document and Track Actions
Act as Central Monitoring subject matter expert
Provide Oversight of Contract Research Organization (CRO) Activities

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

Central Monitoringdata analysisrisk assessmentdata managementquality controlauditing proceduresmathematical concepts

Soft Skills

written communication