Manager, Central Monitoring/Senior Central Monitoring Associate - FSP - Remote
Job Overview
Location
2 Locations
Job Type
Full-time
Category
HR & Recruiting
Date Posted
April 16, 2026
Full Job Description
đź“‹ Description
- • Manager, Central Monitoring/Senior Central Monitoring Associate - FSP - Remote is a fully remote home-based role based in the UK or Ireland, responsible for leading centralized monitoring activities for global and complex clinical trials within Parexel’s Functional Service Provider (FSP) program.
- • The role involves developing and authoring Central Monitoring Plans, overseeing execution of Risk-Based Quality Management (RBQM) systems, analyzing Key Risk Indicators (KRIs) and Key Performance Indicators (KPIs) using analytical tools like CluePoints, presenting findings to clinical study teams, facilitating risk-based decisions, documenting actions, and serving as a subject matter expert during audits and inspections.
- • You will collaborate on Study Quality Risk Assessments, partner with CROs to ensure alignment of monitoring strategies, and support multiple studies within a therapeutic area and program-level, contributing directly to patient safety and trial integrity.
- • Parexel is a global leader in biopharmaceutical services, supporting clinical trials for many of today’s top-selling drugs and niche therapies alike, with a mission to improve global health through empathy-driven, scientifically rigorous work.
- • In this role, you will deepen your expertise in RBQM, data analytics, and clinical trial oversight, gain influence across cross-functional teams, and play a pivotal role in ensuring study quality and regulatory compliance while advancing your career in a mission-driven organization.
🎯 Requirements
- • At least 7 years of relevant experience in the biotechnology/pharmaceutical industry, with a minimum of 1 year of direct Central Monitoring experience; site monitoring or data management experience is essential.
- • Experience using CluePoints is essential for configuring, implementing, and executing Central Monitoring RBQM systems.
- • Excellent written communication skills, with the ability to convey complex technical and analytical insights clearly and concisely to diverse audiences.
- • Aptitude for mathematical concepts, statistical methodologies, and data analytics, particularly in interpreting KRIs and KPIs from analytical tools.
- • Knowledge and experience with clinical databases, electronic data capture (EDC) systems, quality control processes, and auditing procedures.
🏖️ Benefits
- • Fully remote home-based position offering flexibility and work-life balance from the UK or Ireland.
- • Opportunity to work on high-impact global clinical trials contributing to the development of life-changing therapies.
- • Access to Parexel’s extensive network and resources, including training and professional development in RBQM and clinical data analytics.
- • Role as a recognized subject matter expert, enhancing visibility and credibility within study teams and during regulatory interactions.
- • Collaborative, mission-driven culture focused on improving patient outcomes through scientific excellence and empathy.
Skills & Technologies
About Parexel International Corporation
Parexel provides global biopharmaceutical services, managing Phase I-IV clinical trials, regulatory consulting, market access, and real-world evidence studies for drug and device development. The company supports sponsors in trial design, site selection, patient recruitment, data management, biostatistics, pharmacovigilance, and health economics. Operating in over 100 countries, Parexel integrates therapeutic expertise with technology platforms to accelerate approvals and improve evidence generation. Services span oncology, neurology, rare diseases, and vaccines, combining decentralized trial capabilities, digital health tools, and post-marketing surveillance to optimize development timelines and commercial success.
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