Remote Clinical Data Engineer - SAS & CMA Lead

Linqia, Inc.; Badajoz; Remote; EUR 45,000 - 75,000; Full time

Job summary

IQVIA seeks a Clinical Monitoring Analyst (Cluepoints) for a remote position with global study exposure. You will implement and refresh the Centralized Monitoring platform, program QTL and data quality checks, and work closely with sponsors, CM leads and data management teams to ensure robust monitoring and timely signal detection.

Role requires SAS proficiency, knowledge of Cluepoints, and strong communication skills to coordinate across regions.

Qualifications

• 3+ years of experience in pharmaceutical R&D or related field, preferably centralized monitoring, data management or biostatistics.
• 2-3 years SAS experience including macro language.
• Experience with Cluepoints platform.
• Ability to work autonomously and engage stakeholders in study-level centralized monitoring.

Responsibilities

• Maintain and support the Centralized Monitoring process according to the CMP.
• Set up and program QTL, KRI and Data Quality Assessments.
• Refresh CM Platform at predefined frequency to enable signal identification.
• Generate and maintain CM platform specifications and file in eTMF.
• Review study protocol and understand data sources, transfer specs and data structure.
• Collaborate with CMA colleagues for peer-review of CM platform setups.

Skills

SAS programming

Cluepoints

Data management

Clinical Data Management

Communication skills

English proficiency

Relational databases

Job description

IQVIA seeks a Clinical Monitoring Analyst (Cluepoints) for a remote position with global study exposure. You will implement and refresh the Centralized Monitoring platform, program QTL and data quality checks, and work closely with sponsors, CM leads and data management teams to ensure robust monitoring and timely signal detection.

Role requires SAS proficiency, knowledge of Cluepoints, and strong communication skills to coordinate across regions.