Manager, Central Monitoring – Senior Central Monitoring Associate
Parexel
full-time
Posted on:
Location Type: Remote
Location: United Kingdom
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Job Level
About the role
- 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
- 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
- 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
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
Central Monitoringdata analysisrisk assessmentdata managementquality controlauditing proceduresmathematical concepts
Soft Skills
written communication