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Senior Clinical Programmer (Standards)


Chennai, TN 600006
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Job Details


+ A highly productive, independent programming lead ensuring excellence in the delivery of clinical and data management ad hoc listings

+ Ensures excellence in the programming of analysis ready datasets, tables, listings, and figures for which they are responsible

+ Ensures adherence to high quality programming standards in their daily work


+ Accountable for the quality and timely delivery of enterprise, study and asset level deliverables of standard and ad hoc clinical listings

+ Experience extracting data from EDC systems (i.e., OC/RDC, InForm, or Rave)

+ Experience with JReview and SpotFire is required

+ Works with clinicians, statisticians, data managers, programming resources and other colleagues as appropriate to ensure clear specifications for programmed deliverables are in place

+ Exhibits routine and occasionally complex problem solving skills, seeking direction when appropriate

+ Works with statisticians and programming leads to ensure clear specifications for their programmed deliverables are in place.

+ May contribute to department level initiatives


+ Bachelor or Master (preferred) Degree in Statistics, Biological Sciences, IT, or related field

+ At least 3 years of hands-on clinical programming experience working with SAS, JReview and Spotfire within a pharmaceutical, biotech, CRO, or Regulatory Agency

+ Clinical trials expertise with an understanding of data operations required for the reporting of clinical trial data

+ Good understanding of ICH and regulatory guidelines

+ Working knowledge of clinical data and relevant data standards

+ Strong written and oral communication skills, and project management skills

+ Proven ability to operate with limited oversight

+ Proven ability to manage delivery under tight timelines

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
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