
10,000+ employees
Founded 1983
💼 Consulting
🏥 Healthcare
📦 Logistics
💰 Venture Round on 1990-01
Consulting • Healthcare • Logistics
Parexel is one of the world's largest clinical research organizations (CROs), providing comprehensive services for the clinical development process from Phase I to IV. The company specializes in portfolio management, clinical trial management, regulatory strategy, market access, and lifecycle management for biopharmaceuticals. Parexel aims to speed life-changing medicines to market by leveraging its clinical, regulatory, and therapeutic expertise. With a global team of over 21,000 professionals, Parexel works to integrate patient insights and innovative trial designs to develop treatments across therapeutic areas such as oncology, neuroscience, rare diseases, and more. It focuses on delivering patient-centric and efficient clinical trials.
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Where this job comes from
Posted on Parexel's careers page, not through a job board
First seen by Remote Rocketship 0 minutes ago

10,000+ employees
Founded 1983
💼 Consulting
🏥 Healthcare
📦 Logistics
💰 Venture Round on 1990-01
Consulting • Healthcare • Logistics
Parexel is one of the world's largest clinical research organizations (CROs), providing comprehensive services for the clinical development process from Phase I to IV. The company specializes in portfolio management, clinical trial management, regulatory strategy, market access, and lifecycle management for biopharmaceuticals. Parexel aims to speed life-changing medicines to market by leveraging its clinical, regulatory, and therapeutic expertise. With a global team of over 21,000 professionals, Parexel works to integrate patient insights and innovative trial designs to develop treatments across therapeutic areas such as oncology, neuroscience, rare diseases, and more. It focuses on delivering patient-centric and efficient clinical trials.
• Participate in developing and refining the Study Quality Risk Assessment and Control Tracker (QRACT) to identify and manage study risks • Lead creation of the Central Monitoring Plan aligned with study-specific needs and RBQM methodologies • Work with data analysts to configure, implement, and execute the Central Monitoring RBQM system across assigned studies • Conduct study-level Central Monitoring Reviews using data analysis tools • Interpret KRIs/KPIs and assess trends to identify areas requiring intervention • Present findings to clinical study teams, support root cause analysis, and recommend follow-up actions • Document Central Monitoring Review outputs, track decisions, and ensure timely closure of actions • Act as Central Monitoring subject matter expert during audits, inspections, and within study teams • Partner with outsourcing management to align monitoring strategies and oversee CRO execution of Central Monitoring activities • Evaluate processes and recommend improvements to tools, metrics, and methodologies • Represent Central Monitoring in cross-functional process improvement initiatives and assess emerging technologies
• Bachelor’s Degree or equivalent experience required • At least 7 years of relevant experience in the biotechnology/pharmaceutical industry • Minimum of 1 year of direct Central Monitoring experience • Strong analytical problem-solving and critical thinking abilities • Experience troubleshooting data refreshes and resolving execution errors in analytical systems • Working knowledge of the clinical drug development process, including ICH, GCP guidelines, and regulatory requirements • Effective communication and interpersonal skills; ability to build relationships internally and externally • Ability to identify and interpret current and future business trends and apply them to centralized monitoring practices • Excellent written communication skills and ability to convey complex technical and analytical insights clearly and concisely • Aptitude for mathematical concepts, statistical methodologies, and data analytics, with a focus on interpreting KRIs and KPIs • Knowledge and experience with clinical databases, electronic data capture systems, quality control processes, and auditing procedures • Proficiency in Microsoft Office applications, with advanced Excel skills for data manipulation and reporting • Experience using CluePoints or a similar centralized monitoring system preferred • Site monitoring or data management experience is a plus
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