Clinical Programmer

Responsibilities :

• Provide clinical programming expertise to support clinical trials, global filings, regulatory queries, data collection, and cleaning.
• Provide input from statistical programming to support clinical trials, global filings, regulatory queries, labelling, and payer analyses, as well as scientific communications and publications.
• Offer subject matter expertise to the design of data collection, data cleaning, SAP, and TFL mock shells.
• Collaborate with cross-functional groups to ensure the successful execution of clinical trials.
• Create, validate, or review SDTM, ADaM, and TFLs, mapping specifications, and variable definitions.
• Review CSR analysis outputs and evaluate submission data packages.
• Program, test, and document utility programs and tools per standard procedures.
• Support daily operations, ensuring all assigned project tasks are completed accurately and on schedule.
• Contribute to departmental process development and process improvement.
• Patient Reported Outcomes (PROs).
• Clinical Systems.
• Data collection.
• Data Cleaning.
• Building a culture of care, engagement, and recognition with clear outcomes.

Requirements :