Sr Manager, Biostatistics

Location
Foster City
Salary
See job description.
Posted
October 21 2020
Ref
R0014922
Position Type
Full Time
Organization Type
Pharma
Job Type
Manager


Sr Manager, Biostatistics
United States - California - Foster City

Gilead Sciences, Inc. is a research-based bio-pharmaceutical company that discovers, develops and commercializes innovative medicines in areas of unmet medical need. With each new discovery and investigational drug candidate, we seek to improve the care of patients living with life-threatening diseases around the world. Gileads therapeutic areas of focus include HIV/AIDS, liver diseases, cancer and inflammation, and serious respiratory and cardiovascular conditions.

Making an impact on a global scale
Inclusion is one of the companys five core values. Thats because we know that we are stronger and more innovative at Gilead when we are informed by a diverse set of backgrounds, experiences and points of view. Gilead Sciences is a biopharmaceutical company that discovers, develops and commercializes innovative therapeutics in areas of unmet medical need. The company's mission is to advance the care of patients suffering from life-threatening diseases worldwide.

When you join Gilead, you join our mission to change the world by enabling people to live healthier and more fulfilling lives. Come join a mission-driven bio-pharmaceutical organization that values inclusion and diversity, has a strong portfolio of products, and is constantly #CreatingPossible


Biostatisticians work collaboratively with internal and external colleagues to ensure appropriate design, statistical analysis and reporting of Gilead clinical data in efficiently achieving regulatory, scientific and business objectives. Primarily responsible for the business, operational, and compliance aspects of drug discovery, development, and marketed products at Gilead.

Key Skills
  • Leads the statistical analysis, document review, and data interpretation for inclusion in NDA submissions.
  • Oversees and contributes to the completion of all technical and operational statistical activities for a group of clinical trials.
  • Is a point of influence in setting strategy for the group.
  • Defends results and analysis externally.


  • Job Responsibilities
    • Works collaboratively with Statistical Programmers, Biostatisticians, Clinical Research Associates, Clinical Data Managers and other Clinical, Global Drug Safety, Regulatory and Project Management staff to meet project deliverables and timelines for statistical data analysis and reporting.
    • Directs internal and external teams across multifunctional project or functional areas, leads initiatives to gather, organize, and analyze data from different sources such as virology, Case Report Forms, and patient tracking; and works with management and Human Resources to satisfy short-term staffing needs.
    • Is expected to oversee and contribute to the completion of all technical and operational statistical activities for a group of clinical trials for a compound/indication or equivalent through management of internal and external resources.
    • Provides senior level review of various technical documents.
    • Excellent verbal and written communication skills and interpersonal skills are required.
    • Offers advice to others within the company to help make better decisions and resolve problems.
    • Ability to examine issues from various perspectives and apply appropriate concepts to address situations.
    • Must be able to determine the functions most critical to company success and to support priorities within functional area.
    • Addresses obstacles and difficulties of clients in order to meet goals.
    • Can pull together highly effective teams and create a clear sense of direction.


  • Education and Experience
    • 8 years of industry experience in the statistical analysis of biomedical data using SAS software and a BS degree in Biostatistics or equivalent.
    • 4+ years of industry experience in the statistical analysis of biomedical data using SAS software and an MS degree in Biostatistics or equivalent
    • 2+ year of industry experience in the statistical analysis of biomedical data using SAS software and a PhD degree in Biostatistics or equivalent.

For jobs in the United States:

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. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans' Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation in the job application process may contact careers@gilead.com for assistance.

For more information about equal employment opportunity protections, please view the EEO is the Law' poster.

NOTICE: EMPLOYEE POLYGRAPH PROTECTION ACT
YOUR RIGHTS UNDER THE FAMILY AND MEDICAL LEAVE ACT

PAY TRANSPARENCY NONDISCRIMINATION PROVISION

Our environment respects individual differences and recognizes each employee as an integral member of our company. Our workforce reflects these values and celebrates the individuals who make up our growing team.

Gilead provides a work environment free of harassment and prohibited conduct. We promote and support individual differences and diversity of thoughts and opinion.

For Current Gilead Employees and Contractors:

Please log onto your Internal Career Site to apply for this job.


To apply, visit https://gilead.wd1.myworkdayjobs.com/en-US/gileadcareers/job/United-States---California---Foster-City/Sr-Manager--Biostatistics_R0014922-2





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