Biostatistical Programming Senior Associate Job at Amgen (Hyderabad)

Biostatistical Programming Senior Associate

Amgen is expanding its global Statistical Programming capabilities, with Amgen I...

Location

India , Hyderabad

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

BA/BSc or higher degree in biostatistics, statistics, mathematics, computer science, or other related quantitative or scientific subjects
At least 4 years of statistical programming experience in a clinical development environment
Familiarity with drug development life cycle
Excellent skills with the manipulation, analysis and reporting of complex clinical trial data
Ability to effectively perform complex statistical programming and related tasks
Ability to provide quality output and deliverables in adherence with challenging timelines
Ability to work effectively on multiple tasks or projects across therapeutic areas
Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners
Working knowledge of latest CDISC SDTM standards
Familiar with CDISC ADaM and Define standards with strong ability to implement the standards

Job Responsibility

Perform hands on statistical programming activities to support complex statistical data analysis of clinical studies and regulatory submissions
Analysis and reporting of clinical trial data using SAS and/or R
Creation and validation of complex SDTM, ADaM, and other analysis datasets, both safety and efficacy
Creation and validation of complex tables, listings, and figures, both safety and efficacy
Prepare statistical programming specifications
Prepare statistical programming related documents for regulatory submissions
Maintain tracking and validation documentation
Collaborate with cross-functional team and create and/or validate complex programs for checking data quality
Interact and collaborate with study team members from other functions globally
Assist in some of the tasks of the Study Lead Programmer (SLP) or serve as a backup SLP

What we offer

Vast opportunities to learn and move up and across our global organization
Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits

Biostatistical Programming Senior Associate

Amgen is expanding its global Statistical Programming capabilities, with Amgen I...

Location

India , Hyderabad

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

BA/BSc or higher degree in biostatistics, statistics, mathematics, computer science, or other related quantitative or scientific subjects
At least 4 years of statistical programming experience in a clinical development environment
Familiarity with drug development life cycle
Excellent skills with the manipulation, analysis and reporting of complex clinical trial data
Ability to effectively perform complex statistical programming and related tasks
Ability to provide quality output and deliverables in adherence with challenging timelines
Ability to work effectively on multiple tasks or projects across therapeutic areas
Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners
Working knowledge of latest CDISC SDTM standards
Familiar with CDISC ADaM and Define standards with strong ability to implement the standards

Job Responsibility

Perform hands on statistical programming activities to support complex statistical data analysis of clinical studies and regulatory submissions
Analysis and reporting of clinical trial data using SAS and/or R
Creation and validation of complex SDTM, ADaM, and other analysis datasets, both safety and efficacy
Creation and validation of complex tables, listings, and figures, both safety and efficacy
Prepare statistical programming specifications
Prepare statistical programming related documents for regulatory submissions
Maintain tracking and validation documentation
Collaborate with cross-functional team and create and/or validate complex programs for checking data quality
Interact and collaborate with study team members from other functions globally
Assist in some of the tasks of the Study Lead Programmer (SLP) or serve as a backup SLP

What we offer

Vast opportunities to learn and move up and across our global organization
Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits

Biostatistical Programming Senior Associate

Amgen is expanding its global Statistical Programming capabilities, with Amgen I...

Location

India , Hyderabad

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

BA/BSc or higher degree in biostatistics, statistics, mathematics, computer science, or other related quantitative or scientific subjects
At least 4 years of statistical programming experience in a clinical development environment
Familiarity with drug development life cycle
Excellent skills with the manipulation, analysis and reporting of complex clinical trial data
Ability to effectively perform complex statistical programming and related tasks
Ability to provide quality output and deliverables in adherence with challenging timelines
Ability to work effectively on multiple tasks or projects across therapeutic areas
Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners
Working knowledge of latest CDISC SDTM standards
Familiar with CDISC ADaM and Define standards with strong ability to implement the standards

Job Responsibility

Perform hands on statistical programming activities to support complex statistical data analysis of clinical studies and regulatory submissions
Analysis and reporting of clinical trial data using SAS and/or R
Creation and validation of complex SDTM, ADaM, and other analysis datasets, both safety and efficacy
Creation and validation of complex tables, listings, and figures, both safety and efficacy
Prepare statistical programming specifications
Prepare statistical programming related documents for regulatory submissions
Maintain tracking and validation documentation
Collaborate with cross-functional team and create and/or validate complex programs for checking data quality
Interact and collaborate with study team members from other functions globally
Assist in some of the tasks of the Study Lead Programmer (SLP) or serve as a backup SLP

What we offer

Vast opportunities to learn and move up and across our global organization
Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits

Biostatistical Programming Senior Associate

Amgen is expanding its global Statistical Programming capabilities, with Amgen I...

Location

India , Hyderabad

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

BA/BSc or higher degree in biostatistics, statistics, mathematics, computer science, or other related quantitative or scientific subjects
At least 4 years of statistical programming experience in a clinical development environment
Familiarity with drug development life cycle
Excellent skills with the manipulation, analysis and reporting of complex clinical trial data
Ability to effectively perform complex statistical programming and related tasks
Ability to provide quality output and deliverables in adherence with challenging timelines
Ability to work effectively on multiple tasks or projects across therapeutic areas
Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners
Working knowledge of latest CDISC SDTM standards
Familiar with CDISC ADaM and Define standards with strong ability to implement the standards

Job Responsibility

Perform hands on statistical programming activities to support complex statistical data analysis of clinical studies and regulatory submissions
Analysis and reporting of clinical trial data using SAS and/or R
Creation and validation of complex SDTM, ADaM, and other analysis datasets, both safety and efficacy
Creation and validation of complex tables, listings, and figures, both safety and efficacy
Prepare statistical programming specifications
Prepare statistical programming related documents for regulatory submissions
Maintain tracking and validation documentation
Collaborate with cross-functional team and create and/or validate complex programs for checking data quality
Interact and collaborate with study team members from other functions globally
Assist in some of the tasks of the Study Lead Programmer (SLP) or serve as a backup SLP

What we offer

Vast opportunities to learn and move up and across our global organization
Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits

Biostatistical Programming Senior Associate

Amgen is expanding its global Statistical Programming capabilities, with Amgen I...

Location

India , Hyderabad

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

BA/BSc or higher degree in biostatistics, statistics, mathematics, computer science, or other related quantitative or scientific subjects
At least 4 years of statistical programming experience in a clinical development environment
Familiarity with drug development life cycle
Excellent skills with the manipulation, analysis and reporting of complex clinical trial data
Ability to effectively perform complex statistical programming and related tasks
Ability to provide quality output and deliverables in adherence with challenging timelines
Ability to work effectively on multiple tasks or projects across therapeutic areas
Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners
Working knowledge of latest CDISC SDTM standards
Familiar with CDISC ADaM and Define standards with strong ability to implement the standards

Job Responsibility

Perform hands on statistical programming activities to support complex statistical data analysis of clinical studies and regulatory submissions
Analysis and reporting of clinical trial data using SAS and/or R
Creation and validation of complex SDTM, ADaM, and other analysis datasets, both safety and efficacy
Creation and validation of complex tables, listings, and figures, both safety and efficacy
Prepare statistical programming specifications
Prepare statistical programming related documents for regulatory submissions
Maintain tracking and validation documentation
Collaborate with cross-functional team and create and/or validate complex programs for checking data quality
Interact and collaborate with study team members from other functions globally
Assist in some of the tasks of the Study Lead Programmer (SLP) or serve as a backup SLP

What we offer

Vast opportunities to learn and move up and across our global organization
Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits

Fulltime

Biostatistical Programming Senior Associate

Amgen is expanding its global Statistical Programming capabilities, with Amgen I...

Location

India , Hyderabad

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

BA/BSc or higher degree in biostatistics, statistics, mathematics, computer science, or other related quantitative or scientific subjects
At least 4 years of statistical programming experience in a clinical development environment
Familiarity with drug development life cycle
Excellent skills with the manipulation, analysis and reporting of complex clinical trial data
Ability to effectively perform complex statistical programming and related tasks
Ability to provide quality output and deliverables in adherence with challenging timelines
Ability to work effectively on multiple tasks or projects across therapeutic areas
Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners
Working knowledge of latest CDISC SDTM standards
Familiar with CDISC ADaM and Define standards with strong ability to implement the standards

Job Responsibility

Perform hands on statistical programming activities to support complex statistical data analysis of clinical studies and regulatory submissions
Analysis and reporting of clinical trial data using SAS and/or R
Creation and validation of complex SDTM, ADaM, and other analysis datasets, both safety and efficacy
Creation and validation of complex tables, listings, and figures, both safety and efficacy
Prepare statistical programming specifications
Prepare statistical programming related documents for regulatory submissions
Maintain tracking and validation documentation
Collaborate with cross-functional team and create and/or validate complex programs for checking data quality
Interact and collaborate with study team members from other functions globally
Assist in some of the tasks of the Study Lead Programmer (SLP) or serve as a backup SLP

What we offer

Vast opportunities to learn and move up and across our global organization
Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits

Biostatistical Programming Senior Associate

Amgen is expanding its global Statistical Programming capabilities, with Amgen I...

Location

India , Hyderabad

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

BA/BSc or higher degree in biostatistics, statistics, mathematics, computer science, or other related quantitative or scientific subjects
At least 4 years of statistical programming experience in a clinical development environment
Familiarity with drug development life cycle
Excellent skills with the manipulation, analysis and reporting of complex clinical trial data
Ability to effectively perform complex statistical programming and related tasks
Ability to provide quality output and deliverables in adherence with challenging timelines
Ability to work effectively on multiple tasks or projects across therapeutic areas
Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners
Working knowledge of latest CDISC SDTM standards
Familiar with CDISC ADaM and Define standards with strong ability to implement the standards

Job Responsibility

Perform hands on statistical programming activities to support complex statistical data analysis of clinical studies and regulatory submissions
Analysis and reporting of clinical trial data using SAS and/or R
Creation and validation of complex SDTM, ADaM, and other analysis datasets, both safety and efficacy
Creation and validation of complex tables, listings, and figures, both safety and efficacy
Prepare statistical programming specifications
Prepare statistical programming related documents for regulatory submissions
Maintain tracking and validation documentation
Collaborate with cross-functional team and create and/or validate complex programs for checking data quality
Interact and collaborate with study team members from other functions globally
Assist in some of the tasks of the Study Lead Programmer (SLP) or serve as a backup SLP

What we offer

Vast opportunities to learn and move up and across our global organization
Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits

Biostatistical Programming Senior Associate

Amgen is expanding its global Statistical Programming capabilities, with Amgen I...

Location

India , Hyderabad

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

BA/BSc or higher degree in biostatistics, statistics, mathematics, computer science, or other related quantitative or scientific subjects
At least 4 years of statistical programming experience in a clinical development environment
Familiarity with drug development life cycle
Excellent skills with the manipulation, analysis and reporting of complex clinical trial data
Ability to effectively perform complex statistical programming and related tasks
Ability to provide quality output and deliverables in adherence with challenging timelines
Ability to work effectively on multiple tasks or projects across therapeutic areas
Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners
Working knowledge of latest CDISC SDTM standards
Familiar with CDISC ADaM and Define standards with strong ability to implement the standards

Job Responsibility

Perform hands on statistical programming activities to support complex statistical data analysis of clinical studies and regulatory submissions
Analysis and reporting of clinical trial data using SAS and/or R
Creation and validation of complex SDTM, ADaM, and other analysis datasets, both safety and efficacy
Creation and validation of complex tables, listings, and figures, both safety and efficacy
Prepare statistical programming specifications
Prepare statistical programming related documents for regulatory submissions
Maintain tracking and validation documentation
Collaborate with cross-functional team and create and/or validate complex programs for checking data quality
Interact and collaborate with study team members from other functions globally
Assist in some of the tasks of the Study Lead Programmer (SLP) or serve as a backup SLP

What we offer

Vast opportunities to learn and move up and across our global organization
Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits

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Biostatistical Programming Senior Associate

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Biostatistical Programming Senior Associate

Biostatistical Programming Senior Associate

Biostatistical Programming Senior Associate

Biostatistical Programming Senior Associate

Biostatistical Programming Senior Associate

Biostatistical Programming Senior Associate

Biostatistical Programming Senior Associate

Biostatistical Programming Senior Associate

Biostatistical Programming Senior Associate

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