# Centralized Monitoring Analyst (CMA)

**Company**: IQVIA
**Experience**: senior
**Job type**: full-time
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/London-United-Kingdom/Clinical-Monitoring-Analyst--Cluepoints----Remote_R1513972-1?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_f637ce8f-bc9

## Description

We are seeking a Centralized Monitoring Analyst (CMA) to join our team as a Lead programmer on Cluepoints. As a CMA, you will contribute 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:

- Supporting the Centralized Monitoring Lead (CML) in the development of the fit-for-purpose CM strategy

- Setting up and programming QTL, KRI and Data Quality Assessments according to the study CMP

- Refreshing the Centralized Monitoring Platform at predefined frequency to enable signal identification

- Generating and maintaining the Centralized Monitoring Platform specifications document and filing it in eTMF

- Reviewing and understanding the protocol

- Understanding the data sources for the study, the data transfer specifications and the data structure

- Executing and documenting peer-review of CM platform setup done by other CMA colleagues

Requirements:

- At least 3 years of relevant experience in pharmaceutical research and development or a related field

- 2-3 years of SAS experience, including macro language

- Knowledge and experience working on Cluepoints

- Ability to work autonomously and engage with relevant stakeholders

- Strong communication, interpersonal, organisational and problem-solving skills

- High levels of initiative, drive and commitment

- Prior experience in a Data Management related field is required

- Experience with relational databases, preferably Clinical Data Management and EDC Systems

- Advanced knowledge of federal regulations, Good Clinical Practice, and Good Clinical Data Management Practices

- Excellent command of English

## Skills

### Required
- SAS
- Cluepoints
- Data Management
- Clinical Data Management
- EDC Systems
- Good Clinical Practice
- Good Clinical Data Management Practices

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Source: [Apply at iqvia.wd1.myworkdayjobs.com](https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/London-United-Kingdom/Clinical-Monitoring-Analyst--Cluepoints----Remote_R1513972-1?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)