Statistical Programmer

Biocon Biologics; Bengaluru; On-site; INR 1,000,000 - 1,500,000; Full time

Job summary

A leading pharmaceutical company in Bengaluru is seeking a Biostatistician cum Statistical Programmer to manage biostatistical and SAS programming for clinical trials. The ideal candidate will have over 6 years of experience, strong SAS skills, and a Master's in statistics. This role involves collaborating with a cross-functional team and contributing to research design and analysis strategies. The position offers an opportunity to work on a variety of projects in a dynamic setting.

Qualifications

• 6+ years of experience in a programming role, preferably in clinical trials.
• Strong SAS programming skills and experience in statistical programming.
• Knowledge of applied statistics including parametric and non-parametric methods.

Responsibilities

• Provide SAS programming support to clinical projects from Phase 1 to 4.
• Create programming-related SOPs and manage programming CROs.
• Develop and validate datasets, analysis files, and generate reports.

Skills

SAS programming

Statistical analysis

Data manipulation

Knowledge of CDISC

Project management

Education

Master's degree in statistics

Tools

SAS

R

Job description

Direct message the job poster from Biocon Biologics

Global Talent Acquisition Specialist @BioconBiologics | End to End Recruitment | Pharma/Biotech |

Biostatistician cum Statistical Programmer

Job Description

Performs biostatistical and SAS programming activities for given clinical trials involving Novel, Biosimilar and PMS studies. As a Biostatistician cum Statistical Programmer you’ll work on a variety of projects, while collaborating with our cross-functional team of experts. You’ll be able to develop your statistical skills, gain exposure to multiple therapeutic areas. You’ll also contribute to research design and analytical strategies, provide input into protocols, Statistical Methodology and develop and review statistical analysis plans. As a Statistical Programmer, you will leverage your SAS programming skills to support Phase I-IV clinical trials. with expertise in CDISC implementation (SDTMs, ADaMs) & TFLs, and experience in Regulatory Submissions as a part of the Statistical Programming, will play a key role in supporting a growing pipeline across multiple therapeutic areas, with emphasis on regulatory submissions.

Responsibilities

• Provide SAS programming support to all clinical projects (Phase 1 to 4). Manage programming CROs providing oversight for programming deliverables. Create programming related SOPs, as necessary. Works in tandem with CRO' s Biostatistics and SAS Programming and Data Management teams on various clinical projects.

• Provide statistical input into and review of statistical deliverables (i.e. analysis plans, table shells, programming and table specifications, data review, tables, listings, figures, and statistical sections for integrated reports).

• Performing data manipulation, analysis and reporting of clinical trial data, both safety and efficacy, utilizing SAS programming. Applying your SAS programming skills, to create and validate datasets/analysis files, tables, listings, and figures ( TLF s). Generating complex ad-hoc reports for publications.

• Reviews/Develops SAS macros, templates and utilities for data cleaning and reporting. Reviews/ analyses specified in the protocol or the Statistical Analysis Plan (SAP) is implemented while working with the biostatisticians.

• Reviews CRF annotations and data specifications & discuss data structures and participate in data review activities.

• Provide input into statistical programming solutions and/or ensure their efficient implementation. In consultation with the Biostatistician, responsible for reviewing of programming specifications of analysis datasets and pooled datasets.

• 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 guidance. Performs quality control on final reports. Ensures the accuracy of statistical programming components of scientific reports and/or publications with high quality.

• Contributes to assigned parts of process improvement, standardization and other non-clinical initiatives

Technical / Functional Skills

Knowledge of applied parametric and non-parametric statistics, Mixed Model. Missing Data analysis, General Linear models - ANOVA, ANCOVA, t-test, etc Non-Parametric methods - Binomial test, Chi-Squared test, Wilcoxon tests; Logistic regression. Strong SAS/R programming Skills in R software. Advanced SAS and other statistical computing software skills in a clinical data environment across multiple therapeutic areas. Good Knowledge of CDISC implementation (SDTMs, ADaMs)

• Master degree in statistics with Ideally 6+years of work experience in a programming role preferably clinical trials/ or in pharmaceutical industry or CROs.

• Good SAS experience and proven skills in the use of SAS within a Statistical Programming environment to develop and validate deliverables.

Seniority level

• Seniority level

  Associate

Employment type

• Employment type

  Full-time

Job function

• Job function

  Health Care Provider

• Industries

  Pharmaceutical Manufacturing

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