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Senior Associate, Senior Statistical Data Scientist

6 - 7 years

18 - 19 Lacs

Mumbai

Posted:3 months ago| Platform: Naukri logo

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Skills Required

Statistical programming CRO SAS Pharma Project management Clinical trials Management SDLC clinical data ICH

Work Mode

Work from Office

Job Type

Full Time

Job Description

ROLE SUMMARY A productive, hand on programmer who applies technical knowledge of CDISC and practical experience to deliver statistical programming deliverables leveraging CDISC constructs: SDTM, ADaM, and Control Terminology 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 ROLE RESPONSIBILTIES Accountable for the quality and timely delivery of enterprise, study and asset level deliverables of standard statistical programming encompassing the following areas: CDISC , ADaM, and TLF generation. Demonstrate experience working as part of a software development team and fundamental SDLC processes. Ensures excellence in the understanding of CDISC IG requirements, NCI Control Terminology, and programming of analysis ready datasets, tables, listings, and figures for which they are responsible. Ensures adherence to Pinnacle 21 CDISC validation checks and high-quality programming standards in their daily work. 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 of software development practices as defined within Pfizer s CDISC development framework. May contribute to department level initiatives. QUALIFICATIONS Bachelor or Master (preferred) Degree in Statistics, Biological Sciences, IT, or related field At least 5 years relevant CDISC statistical/clinical programming 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 require. Pfizer CDARS experience desirable. Work Location Assignment: Flexible Work Location Assignment: Flexible Work Location Assignment: Hybrid Medical #LI-PFE

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www.pfizer.com

Pharmaceutical Manufacturing

New York New York

10001 Employees

203 Jobs

    Key People

  • Albert Bourla

    Chairman and CEO

  • Angela Hwang

    Group President, Worldwide Vaccines

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