Clinical Data Programmer II

About the role

The Clinical Data Programmer SAS II (CDP SAS) is responsible for data analysis and business intelligence activities related to study related clinical and operational data for the purpose of facilitating clinical data inspection and quality control, as well as operational performance control of clinical sites by creating reports, visualisations and dashboards for Clinical Data Managers (CDM), Clinical Data Reviewers (CDR), Project Managers (PM) and other clinical study stakeholders.

What you'll do

• The Clinical Data Programmer SAS II (CDPSAS) partners with clinical study teams and other stakeholders to define, develop, validate
• Partner with CDMs, CDRs, PMs and other study stakeholders to define clinical, laboratory
• Manage assigned programming deliverables from requirements gathering and specification through development, testing, deployment
• Extract, integrate, transform and analyse clinical study data from EDC, laboratory, operational and other sources using SAS and relevant technologies
• Develop validated, reusable programs and analytical outputs that support data inspection, reconciliation, clinical and medical review

What you need

• 2–5 yrs of experience
• SAS
• Clinical data management
• Clinical research
• Quality control
• Data visualisation
• SOP writing
• B.Tech or B.E. or B.Sc or BCA

Good to have

• Power BI
• CRO
• Looker Studio
• SQL
• Python
• R