Clinical Monitoring Analyst (Cluepoints) - Remote
IQVIA
Overview
In this Centralized Monitoring Analyst role within IQVIA’s Cluepoints team, you will set up, program, and refresh the CM platform according to the CMP. You’ll support the Centralized Monitoring Lead by shaping study-specific CM elements such as QTL, KRI, data visualizations, and data quality assessments. You will liaise with sponsor clients to manage deliveries and ensure CM documentation is filed in eTMF. You will work with study data sources and data transfers, applying your SAS expertise in a regulated environment. This is a hands-on, stakeholder-facing role with meaningful impact on data monitoring quality.
Responsibilities- Set up, program, and refresh the Centralized Monitoring platform per study CMP
- Contribute to CM strategy with QTL, KRI, and data quality components
- Generate and maintain CM platform specifications and file in eTMF
- Review and understand study protocol and data sources
- Peer-review CM platform setup performed by colleagues
- Engage with sponsors and stakeholders to deliver CM activities
- Ensure compliance with regulatory requirements and data confidentiality
- Maintain and interpret basic statistical concepts related to CM outputs
- 3+ years in pharmaceutical R&D, centralized monitoring, data management, or biostatistics
- 2-3 years SAS experience including macro language
- Knowledge of Cluepoints
- Ability to work autonomously and manage stakeholder interactions
- Understanding of study data sources and data transfer specifications
- Experience with relational databases and EDC systems
- Excellent verbal and written English communication
- Knowledge of GCP/Good Clinical Data Management Practices
- communication
- interpersonal skills
- organizational skills
- SAS programming including macro language
- Cluepoints knowledge
- Centralized Monitoring platform setup and maintenance
Reference: WJ-747_30989643