Senior Statistical Programmer

Found in: Talent IN C2 - 2 weeks ago

Hyderabad, India Novartis Full time

About the role

: Senior Statistical Programmer

Location – Hyderabad #LI Hybrid

About the Role:The number of New Molecular Entities (NMEs) approvals of potential blockbusters, which Novartis obtained in 2019 alone. We advanced a breath of early programs in our pipeline that addresses significant unmet needs and are looking for passionate and enthusiastic Statistical Programmers with expertise in SDTMs, ADaMs & TFLs, and experience in Regulatory Submissions. As a part of the Statistical Programming unit, you will play a key role in supporting a growing pipeline across multiple therapeutic areas, with emphasis on regulatory submissions. An excellent opportunity to work end-to-end programming from CRF collections through Regulatory submission, you will have an exciting opportunity to learn new technologies (like R) and endorse Statistical Programming as a key contributor in driving the #GO-Digital vision of Novartis.

Key Responsibilities:

• Lead and coordinate activities of all statistical programmers as Trial Programmer for phase I to IV clinical studies or assigned project-level activities. Make statistical programming recommendations at study level.

• Build and maintain effective working relationship with cross-functional teams, discuss status of deliverables and critical programming aspects (timelines, scope), e.g. as member of the Clinical Trial Team (CTT).

• Review eCRF, discuss data structures and participate in data review activities in accordance with the company, department and industry standards (e.g. CDISC). Processes, review and develop programming specifications as part of the analysis plans.

• Provide input into statistical programming solutions and/or ensure their efficient implementation. Responsible for development of programming specifications of analysis datasets and pooled datasets.

• Ensuring timely and quality development and validation of datasets and outputs for CSRs, regulatory submissions/interactions, safety reports, publications or exploratory analyses (as required) in the assigned drug development study/project according to specifications.

• Responsible for quality control and audit readiness of all assigned statistical programming deliverables as well as accuracy and reliability of statistical analysis results. Maintain up-to-date knowledge of programming software (e.g. SAS) as well as industry requirements (e.g. CDISC SDTM/ADaM, eCTD, Define.xml), attend functional meetings and trainings.

• Establish successful working relationship on individual studies with external associates according to agreed contract and internal business guidelines. Contributes to assigned parts of process improvement, standardization and other non-clinical initiatives.

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