Senior Clinical Data Programmer

Role Summary The Senior Clinical Data Programmer 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.

Qualifications

• A graduate qualification in computer science, data science, mathematics, life sciences or a related field.

• A minimum of 5 years’ relevant experience in statistical programming, business intelligence, data analysis or data science within a pharmaceutical company, CRO or EDC software provider.

• Practical experience using SAS and/or business intelligence tools (e.g. TIBCO Spotfire, Power BI), to interrogate clinical, laboratory or operational datasets is required.

• Exposure to additional analytics, RBQM, centralised monitoring or workflow automation platforms is desirable.