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Pfizer

Senior Statistical Data Scientist

Job Posted 7 Days Ago Posted 7 Days Ago
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Hybrid
Chennai, Tamil Nadu
Senior level
Hybrid
Chennai, Tamil Nadu
Senior level
The Senior Statistical Data Scientist is accountable for quality statistical programming deliverables for clinical studies, ensuring adherence to programming standards, documentation, and QC. They collaborate with statisticians, possess extensive experience in pharmaceutical or biotech environments, and may contribute to departmental projects. Strong problem-solving skills and the ability to manage tight timelines are crucial.
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Job Summary :
A productive, hands on programmer who applies technical knowledge and practical experience to• deliver statistical programming deliverables to support assets and study teams with limited supervision• early in role and independently later in role.• 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.
Job Responsibilities :
Accountable for the quality and timely delivery of datasets and displays required for their clinical study• reports as well as other asset level deliverables they may be programming• Ensures appropriate documentation and QC across the lifespan of the study for all of their• programming deliverables• 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.• Will be knowledgeable in core safety standards as well as TA standards pertinent to their project, may• aid in development of standards necessary for their study• May contribute to department level initiatives.
Qualification/ Skills:
. Bachelor or Master (preferred) Degree in Statistics, Biological Sciences, IT, or related field.• At least 4 years relevant experience in a pharmaceutical, biotech, CRO, or Regulatory Agency.• Statistical Programming and SAS hand-on experience• 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• Knowledge of at least 1 Therapeutic Area• Proven ability to manage delivery under tight timelines.• CDISC experience desirable
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
Medical
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Top Skills

SAS
Statistical Programming

Pfizer Chennai, Tamil Nadu, IND Office

Chennai, India

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