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Clinical Monitoring Analyst (Cluepoints) - Remote

May 12, 2026

This unique role within IQVIA lends itself to a Lead programmer on Cluepoints called Centralized Monitoring Analyst (CMA) with strong communication and organisation skills. Having experience with SAS programming is necessary. This role is part of a sponsor dedicated project where you will be working with the client directly to manage deliveries. The CMA contributes to the execution of the Centralized Monitoring process by performing the setup, programming and refresh(es) of the Centralized Monitoring platform, according to the study-specific Centralized Monitoring Plan (CMP). Main responsibilities include:<ul><li>Supports the Centralized Monitoring Lead (CML) in the development of the fit-for purpose CM strategy by contributing to the identification of the relevant CM elements to be implemented for the study (Quality Tolerance Limits (QTL), Key Risk Indicators, data visualizations and Data Quality Assessments)</li><li>Setup/Program QTL, KRI and Data Quality Assessments according to the study CMP</li><li>Refresh the Centralized Monitoring Platform at predefined frequency to enable signal identification</li><li>Generate and maintain the Centralized Monitoring Platform specifications document and file it in eTMF</li><li>Review and understanding of protocol is key</li><li>Understand the data sources for the study, the data transfer specifications and the data structure</li><li>Execute and document peer-review of CM platform setup done by other CMA colleagues</li></ul> Experience:<ul><li>At least 3 years relevant experience in the area of pharmaceutical research and development or related field preferably in centralized Monitoring, data management, and/or biostatistics</li><li> 2-3 years SAS experience including macro language</li><li>Knowledge/ experience working on Cluepoints </li><li>Ability to work in an autonomous way and engage with relevant stakeholders to execute activities related to study level centralized monitoring process.</li><li>Ability to understand basic statistical analysis concepts and to interpret their outcome.</li><li>Ability to maintain confidentiality of data and information during interactions with staff at all levels</li><li> Ability to work with limited close supervision.</li><li>Demonstrated communication, interpersonal, organizational and problem-solving skills</li><li>High levels of initiative, drive and commitment.</li><li> Prior experience in a Data Management related field is required</li><li>Experience with relational databases, preferably Clinical Data Management and EDC Systems</li><li>Experience communicating with all levels of personnel and participating in collaborative work team (locally and globally).</li><li>Advanced knowledge of federal regulations, Good Clinical Practice, and Good Clinical Data Management Practices.</li><li>Excellent command, both verbal and written, of English</li></ul>This role is not eligible for UK visa sponsorshipIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at <a href="https://jobs.iqvia.com/" target="_blank" rel="noopener noreferrer">https://jobs.iqvia.com</a>IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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Common Interview Questions And Answers

1. HOW DO YOU PLAN YOUR DAY?

This is what this question poses: When do you focus and start working seriously? What are the hours you work optimally? Are you a night owl? A morning bird? Remote teams can be made up of people working on different shifts and around the world, so you won't necessarily be stuck in the 9-5 schedule if it's not for you...

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When you're working on a remote team, there's no way to chat in the hallway between meetings or catch up on the latest project during an office carpool. Therefore, virtual communication will be absolutely essential to get your work done...

3. WHAT IS "WORKING REMOTE" REALLY FOR YOU?

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4. WHAT DO YOU NEED IN YOUR PHYSICAL WORKSPACE TO SUCCEED IN YOUR WORK?

With this question, companies are looking to see what equipment they may need to provide you with and to verify how aware you are of what remote working could mean for you physically and logistically...

5. HOW DO YOU PROCESS INFORMATION?

Several years ago, I was working in a team to plan a big event. My supervisor made us all work as a team before the big day. One of our activities has been to find out how each of us processes information...

6. HOW DO YOU MANAGE THE CALENDAR AND THE PROGRAM? WHICH APPLICATIONS / SYSTEM DO YOU USE?

Or you may receive even more specific questions, such as: What's on your calendar? Do you plan blocks of time to do certain types of work? Do you have an open calendar that everyone can see?...

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Just like your schedule, how you track files and other information is very important. After all, everything is digital!...

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