Job Responsibilities:

Perform, plan and co-ordinate the following for complex studies: (i) the programming, testing, and documentation of statistical programs for use in creating statistical tables, figures, and listing summaries and (ii) the programming of analysis databases (derived datasets) and transfers of data for internal and external clients. May perform and plan the programming of database quality control checks.
Program and plan the integration of databases from multiple studies or sources.
Develop and co-ordinate programming documentation including plans and specifications, as appropriate, for complex studies.
Provide advanced technical expertise in conjunction with internal and external clients, and independently bring project solutions to teams and department, for complex studies.
Perform, plan and co-ordinate the development, implementation and validation of new process technologies, macros and applications.
Fulfill project responsibilities at the level of statistical team lead for single complex studies or group of studies.
Understand the Scope of Work, budget and quote assumptions, estimate the work completed, manage Out of Scope and resource forecasts for single studies. May manage project budget and resource requirements and provide revenue forecasts for single studies.
Provide training and guidance to lower-level staff.

Job Qualifications

Master's Degree Computer science or related field and 3 years relevant experience or bachelor's degree Computer science or related field and 4 years relevant experience
Equivalent combination of education, training and experience in lieu of degree
Knowledge of statistics, programming and/or clinical drug development process
Advanced knowledge of computing applications such asBase SAS, SAS Graph and SAS Macro Language
Advance knowledge inSQL and MS Excel
Good organizational, interpersonal, leadership and communication skills
Ability to effectively manage multiple tasks and projects
Excellent accuracy and attention to detail
Ability to establish and maintain effective working relationships with coworkers, managers and clients
Amenable to work on Hybrid set-up in Mckinely, Taguig
Amenable to work on Night shift schedule

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

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Sr Statistical Programmer