Expert Clinical Programmer

Major accountabilities:

• Produce and track reports, analytics or visualizations for various line functions within Global Drug Development, used for ongoing monitoring of clinical data
• Provide understandable and actionable reports on clinical data and monitoring of clinical data for key stakeholders
• Author the user requirements document, functional specifications and functional testing scripts
• Facilitate interaction with end-user on creating specifications and working with programmers or performing the programming activities for successful delivery.
• To provide quantitative analytical support to the global program teams, including providing support on analyzing reports
• Support the planning, execution and close-out of Clinical Programs/Trials.
• Support the management in collation and delivery of analytics reports for critical decision making
• Create, file and maintain appropriate documentation
• Work with the internal SMEs and key stakeholders in providing analysis and interpretation of clinical program/trial operational data
• Provide necessary training to end-user on best / appropriate and consistent use of various data review tools
• Support or lead special projects of limited scope (sub team lead, local project, etc.) both clinical and non-clinical in nature.
• Provide study level expertise and involvement in CTTs.
• Lead or provide support to special projects both clinical and non-clinical in nature or in general areas spanning various responsibilities but not limited to systems issues, processes, user support, training, etc.

Minimum Requirements:

• At least 6 years’ experience in clinical review and reporting programming, business analytics and/or clinical trial setup, gained 
• in the pharmaceutical industry, CRO or Life Science related industry as well as the following:
• Excellent knowledge of programming languages (SQL, PL/SQL, 
• C#, VB script, SAS, Python, R) 
• • Excellent knowledge of Data Review and/or Business Intelligence tools (such as Spotfire, Review)
• Knowledge of clinical data management systems and/or relational databases (e.g. OC/RDC, INFORM, RAVE) as applied to 
• clinical trials 
• Attention to detail, quality, time management and customer focus development. Understanding of Drug Development Process, ICH-GCP, CDISC standards and Health Authority guidelines and regulations.