Clinical Monitoring Analyst

🕒 May 12

🌐 United Kingdom, Hungary, +4 more countries – Remote

🇬🇧 United Kingdom – Remote 🇭🇺 Hungary – Remote 🇿🇦 South Africa – Remote 🇮🇪 Ireland – Remote 🇪🇸 Spain – Remote 🇧🇬 Bulgaria – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

🧐 Analyst

🇬🇧 UK Skilled Worker Visa Sponsor

This company has sponsored UK Skilled Worker visas in the past.

👻 Ghost score 65%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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IQVIA

WebsiteLinkedInAll Job Openings

10,000+ employees

💼 Consulting

🏭 Manufacturing

📣 Marketing

💰 $1G Post-IPO Debt on 2023-05

Consulting • Manufacturing • Marketing

IQVIA is a global leader in data analytics and technology solutions, dedicated to improving health outcomes. The company utilizes its Connected Intelligence platform to harness the power of advanced data analytics and artificial intelligence, facilitating innovation in healthcare. IQVIA focuses on various areas, including clinical research, technology, and consulting services to solve complex healthcare challenges and accelerate the delivery of new therapies to patients.

📋 Description

• Contribute to development of fit-for-purpose centralized monitoring strategies • Identify relevant centralized monitoring elements, including Quality Tolerance Limits, Key Risk Indicators, data visualizations, and Data Quality Assessments • Set up and program QTLs, KRIs, and Data Quality Assessments according to the study Centralized Monitoring Plan • Refresh the Centralized Monitoring Platform at predefined frequencies to enable signal identification • Generate, maintain, and file Centralized Monitoring Platform specifications in the eTMF • Review and understand study protocols • Understand study data sources, transfer specifications, and data structures • Execute and document peer reviews of Centralized Monitoring Platform setups completed by other CMA colleagues • Work directly with the client on deliveries for a sponsor-dedicated project • Support the Centralized Monitoring Lead in study-level centralized monitoring processes

🎯 Requirements

• At least 3 years relevant experience in pharmaceutical research and development or a related field, preferably in centralized monitoring, data management, and/or biostatistics • 2–3 years of SAS experience, including macro language • Knowledge/experience working on Cluepoints • Ability to work autonomously and engage with relevant stakeholders to execute study-level centralized monitoring activities • Ability to understand basic statistical analysis concepts and interpret outcomes • Ability to maintain confidentiality of data and information • Ability to work with limited close supervision • Demonstrated communication, interpersonal, organizational, and problem-solving skills • High levels of initiative, drive, and commitment • Prior experience in a Data Management-related field • Experience with relational databases, preferably Clinical Data Management and EDC systems • Experience communicating with all levels of personnel and participating in collaborative work teams locally and globally • Advanced knowledge of federal regulations, Good Clinical Practice, and Good Clinical Data Management Practices • Excellent verbal and written command of English • This role is not eligible for UK visa sponsorship

🏖️ Benefits

• No benefits or compensation extras specified