Gilead Sciences, Inc.
Sr. Manager, Statistical Programming
Gilead Sciences, Inc., Foster City, California, United States, 94420
Sr. Manager, Statistical Programming
Locations: United States - California - Foster CityTime Type: Full TimePosted on: Vor 2 TagenJob Requisition ID: R0043214At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19, and cancer – working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. Our mission requires collaboration, determination, and a relentless drive to make a difference.Every member of Gilead’s team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we’re looking for the next wave of passionate and ambitious people ready to make a direct impact.Job DescriptionSr. Manager, Statistical ProgrammingKey Skills:Successfully interacts within Clinical Data Science, with Clinical Development and Regulatory Affairs groups on a frequent basis.Viewed as a key resource by more senior individuals on technical initiatives for projects and may represent the Company on contracts.Inform functional management programming resources required for the project.Has experiences in leading studies and deep understanding of end-to-end data standards (e.g., collection, mapping, analysis, reporting, and submission).Has experiences with both late phase (phase II, III) and early phase (e.g., Dose Escalation) studies.Has in-depth knowledge with efficacy validation and efficacy analyses for studies.Recommends and provides trainings.Job Responsibilities:Works collaboratively with Clinical Development staff to meet project deliverables and timelines for statistical data analysis and reporting.Generates or oversees the production of programming deliverables (e.g., tables, listings) for study reports and integrated summaries.Anticipates resource needs and works with management and HR to ensure adequate long-term resource allocation within a project.May manage a small team of programmers.Designs and/or codes analysis files.Ensures programming and corresponding documentation is completed in a manner that is consistent with departmental procedures.Is responsible for all programming activities within a project or equivalent.Is responsible for implementing efficacy validation, efficacy analysis datasets, and TFLs for studies.Provides primary and secondary programming support as needed for projects.Implements strategic initiatives.Excellent verbal and written communication skills and interpersonal skills are required.Has a thorough understanding of clinical trials design and reporting process, as well as regulatory reporting requirements including electronic data submissions.Must be able to interact with others to define and produce user-defined statistical reports (e.g., ad hoc requests).Has the ability to resolve study-related issues and conflicts within a therapeutic project.Can create buy-in and support and has the ability to negotiate timelines.Has the ability to directly supervise personnel.Education and Experience:8 years of experience and a BS degree in Biostatistics/Computer Science or equivalent.4 years of experience and a MS degree in Biostatistics/Computer Science or equivalent.2 years of experience and a PhD degree in Biostatistics/Computer Science or equivalent.The salary range for this position is: $165,580.00 - $214,280.00. Gilead considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives, paid time off, and a benefits package. Benefits include company-sponsored medical, dental, vision, and life insurance plans.For additional benefits information, visit:
Benefits InformationEqual Opportunity Employer
As an equal opportunity employer, Gilead Sciences Inc. is committed to a diverse workforce. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, gender, age, sexual orientation, physical or mental disability, genetic information or characteristic, gender identity and expression, veteran status, or other non-job related characteristics or other prohibited grounds specified in applicable federal, state, and local laws.
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Locations: United States - California - Foster CityTime Type: Full TimePosted on: Vor 2 TagenJob Requisition ID: R0043214At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19, and cancer – working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. Our mission requires collaboration, determination, and a relentless drive to make a difference.Every member of Gilead’s team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we’re looking for the next wave of passionate and ambitious people ready to make a direct impact.Job DescriptionSr. Manager, Statistical ProgrammingKey Skills:Successfully interacts within Clinical Data Science, with Clinical Development and Regulatory Affairs groups on a frequent basis.Viewed as a key resource by more senior individuals on technical initiatives for projects and may represent the Company on contracts.Inform functional management programming resources required for the project.Has experiences in leading studies and deep understanding of end-to-end data standards (e.g., collection, mapping, analysis, reporting, and submission).Has experiences with both late phase (phase II, III) and early phase (e.g., Dose Escalation) studies.Has in-depth knowledge with efficacy validation and efficacy analyses for studies.Recommends and provides trainings.Job Responsibilities:Works collaboratively with Clinical Development staff to meet project deliverables and timelines for statistical data analysis and reporting.Generates or oversees the production of programming deliverables (e.g., tables, listings) for study reports and integrated summaries.Anticipates resource needs and works with management and HR to ensure adequate long-term resource allocation within a project.May manage a small team of programmers.Designs and/or codes analysis files.Ensures programming and corresponding documentation is completed in a manner that is consistent with departmental procedures.Is responsible for all programming activities within a project or equivalent.Is responsible for implementing efficacy validation, efficacy analysis datasets, and TFLs for studies.Provides primary and secondary programming support as needed for projects.Implements strategic initiatives.Excellent verbal and written communication skills and interpersonal skills are required.Has a thorough understanding of clinical trials design and reporting process, as well as regulatory reporting requirements including electronic data submissions.Must be able to interact with others to define and produce user-defined statistical reports (e.g., ad hoc requests).Has the ability to resolve study-related issues and conflicts within a therapeutic project.Can create buy-in and support and has the ability to negotiate timelines.Has the ability to directly supervise personnel.Education and Experience:8 years of experience and a BS degree in Biostatistics/Computer Science or equivalent.4 years of experience and a MS degree in Biostatistics/Computer Science or equivalent.2 years of experience and a PhD degree in Biostatistics/Computer Science or equivalent.The salary range for this position is: $165,580.00 - $214,280.00. Gilead considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives, paid time off, and a benefits package. Benefits include company-sponsored medical, dental, vision, and life insurance plans.For additional benefits information, visit:
Benefits InformationEqual Opportunity Employer
As an equal opportunity employer, Gilead Sciences Inc. is committed to a diverse workforce. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, gender, age, sexual orientation, physical or mental disability, genetic information or characteristic, gender identity and expression, veteran status, or other non-job related characteristics or other prohibited grounds specified in applicable federal, state, and local laws.
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