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Amgen

Makes biotech medicines for serious illnesses

Biostatistical Programming Senior Manager

Quantitative Biology & BiostatisticsConfirmed live in the last 24 hours
Full-timeOregon, USARemote

About the Job

Requirements

  • A doctorate degree and at least 2 years of statistical programming experience in the pharmaceutical industry, or a master's degree and at least 6 years of such experience, or a bachelor's degree and at least 8 years of such experience, or an associate's degree and at least 10 years of such experience, or a high school diploma/GED and at least 12 years of such experience.

Responsibilities

  • Ensure that all statistical aspects pertaining to clinical activities meet required standards and are statistically accurate.
  • Lead a group of Oncology and other therapeutic area products.
  • Be accountable and responsible for Global Statistical Programming study deliverables and submission activities for assigned product areas.
  • Set and drive programming strategies, including functional standards and industry requirements, for assigned product areas globally.
  • Plan and monitor project progress and address issues accordingly.
  • Support and oversee the Global Statistical Programming Functional Service Provider relationship and ensure product goals are met through the provider's staff.
  • Provide product-level input into Global Statistical Programming resource plans and budgets.
  • Monitor and utilize assigned staff at the product level according to priorities.
  • Lead or participate in departmental process-improvement initiatives and cross-functional working groups.
  • Assist with study and system audits and inspections by internal and external bodies.
  • Develop, review, and implement policies, standard operating procedures, and other controlled documents affecting Global Statistical Programming globally.
  • Provide hands-on support to assigned product areas as required.
  • Provide coaching and mentoring to staff.
  • Provide input into career development plans for staff on assigned projects.

Desired Qualifications

  • In-depth knowledge of SAS Graph, SAS/STAT, SAS Macro, and SQL.
  • Advanced SAS analysis and reporting skills.
  • Prior regulatory submission experience.
  • Thorough understanding of and experience with data quality and compliance checks.
  • Experience in software development, including gathering user requirements, creating technical specifications, developing code, and creating and driving test plans.
  • Familiarity with the R programming language.
  • Statistical programming experience in a clinical development environment.
  • Experience working effectively in a globally dispersed team environment with cross-cultural partners.
  • Ability to lead and manage programmers in the successful and timely completion of programming activities for one or multiple studies from end to end.
  • Prior staff-development leadership and project-management experience.
  • Ability to effectively perform complex statistical programming and related tasks.

About the Company

Amgen

Makes biotech medicines for serious illnesses

Amgen develops and makes biologic medicines, which are drugs built from proteins and antibodies grown in living cells, for serious conditions such as heart disease, cancer, and bone loss. Its anemia drug Epogen, approved in 1989, became one of the biotechnology industry's first blockbuster medicines. Amgen grows these drugs in large tanks called bioreactors, and its products include the cholesterol drug Repatha, the bone-building drug Evenity, and the severe asthma drug Tezspire. It earns money by selling these medicines, mostly through large drug wholesalers that supply hospitals and pharmacies. Amgen was founded in 1980 and is based in Thousand Oaks, California.

Company size
10,001+
Company stage
IPO
Headquarters
Thousand Oaks, CA
Founded
1980

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