Security Operations Analyst - 24/7 Detection & Response
Pragmatike · Málaga, Spain ·
COMPENSATION
€•• – ••k
Listed on WeAreDevelopers
- Fully remote (EU/UK/SA)
- SAS + Cluepoints
- Clinical Monitoring
- Client-facing role
- Full time
As a Centralized Monitoring Analyst at IQVIA, you will act as a lead programmer on the Cluepoints platform. You will support the execution of centralized monitoring processes by configuring the system according to study-specific plans and identifying key risk indicators.
You will work autonomously on sponsor-dedicated projects, engaging directly with clients to manage deliveries. Your responsibilities include refreshing monitoring platforms to identify signals and maintaining comprehensive documentation within the electronic Trial Master File.
What you'll do
- Program and set up the Centralized Monitoring platform per study plans
- Define Quality Tolerance Limits and Key Risk Indicators
- Refresh monitoring platforms regularly to enable signal identification
- Generate and file platform specifications documents in eTMF
- Review protocols and understand study data structures
- Peer-review platform setups completed by colleagues
- Collaborate with clients to manage project deliveries
What you'll need
- At least 3 years in pharmaceutical R&D or related fields
- 2-3 years of SAS experience including macro language
- Prior experience in Data Management is required
- Knowledge or experience working with Cluepoints
- Experience with relational databases and EDC Systems
- Advanced knowledge of Good Clinical Practice regulations
- Ability to work autonomously with limited supervision
- Strong communication skills for global team collaboration
Stack
- SAS (Software)
- Cluepoints
- Clinical Data Management
- Relational Databases
- Data Visualization
- EDC Systems
How you'll work
- Full time employment
- Remote work available
- Locations include UK, EU, and South Africa