Amgen Inc

Biostatistical Programming Manager

Amgen Inc$133K — $192K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Master's degree in Applied Science, Mathematics, or a related field.
  • Experience creating and managing annotated Case Report Forms (CRFs) using CDISC SDTM implementation guides.
  • Familiarity with project management principles for coordinating timelines and deliverables.
  • Experience collaborating with external stakeholders like CROs or FSPs.
  • Proficient in preparing submission-ready datasets adhering to CDISC and regulatory standards.
  • Skilled in programming with SAS, R, and Python to develop clinical data outputs.
  • Experience designing automation tools for SDTM production process improvement.

Responsibilities

  • Drive design of Case Report Forms and data collection strategy.
  • Review SDTM datasets and submission documents for analysis.
  • Provide CDISC expertise to the Clinical Study Team and partners.
  • Author and review submission files for SDTM.
  • Conduct data conformance checks and audit pivotal snapshots.
  • Support content management for global standards level.
  • Contribute to development of global standards and Case Report Forms.

Benefits

  • Comprehensive employee benefits package.
  • Retirement and Savings Plan with company contributions.
  • Group medical, dental, and vision coverage.
  • Award-winning time-off plans.
  • Flexible work models, including remote and hybrid options.
Full Job Description
Career Category
Clinical Development
Job Description

Biostatistical Programming Manager

Duties: Drive Case Report Form design and data collection strategy within the Clinical Study Team to influence it for purpose data collection decisions while ensuring successful analysis and submission; Review Study Data Tabulation Model (SDTM) datasets and related specification and submission documents for analysis and regulatory submissions; Provide Clinical Data Interchange Standards Consortium expertise and guidance to the Clinical Study Team including the Global Statistical Programming team and cross functional partners for implementation and mapping; Author and review Study Data Tabulation Model submission files; Review Study Data Tabulation Model data conformance checks output and study team dispositions on selected snapshots as determined by need and perform Study Data Tabulation Model audit for all pivotal snapshots; Support global standards level content management and impact analysis; and Support cross-functional development of global standard, Therapeutic Area, and product-level Case Report Forms. May telecommute.

Requirements: Master's degree (or foreign equivalent) in Applied Science, Mathematics, or a related field & completion of a university-level course, research project, internship, or one year of experience in the following:

1. Creating and managing annotated Case Report Forms (CRFs), reviewer's guides, and conformance documentation using controlled terminology and CDISC SDTM implementation guides;

2. Applying project management principles to coordinate timelines, deliverables related to applications that promote automation and harmonization of SDTM production across the portfolio, and cross-functional dependencies to ensure timely report completion;

3. Collaborating with external stakeholders, including Functional Service Providers (FSPs), Contract Research Organizations (CROs), or contingent workers to deliver study-level programming outputs including SDTM domains, CSDRG, Define.xml, and aCRF;

4. Working with clinical trial datasets to support regulatory submissions and internal analysis across different phases of clinical studies;

5. Preparing submission-ready datasets and documentation following CDISC and regulatory standards, including data mapping and ad hoc analyses;

6. Programming in statistical languages, including SAS, R, and Python, to develop and validate clinical data outputs; and

7. Designing and programmatically developing automation tools for process improvement related to automation and harmonization of SDTM production across the portfolio.

Contact: Interested candidates please apply via https://careers.amgen.com/en/search-jobs and search for job # R-244949

Job type: Full Time position. The annual salary for this position in the U.S. is $133,952.00- $192,690.00 per year. Also, this position offers stock, retirement, medical, life and disability insurance and eligibility for an annual bonus or for sales roles, other incentive compensation. For more details visit https://careers.amgen.com/life-at-amgen/benefits/

What you can expect of us

As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we'll support your journey every step of the way.

The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.

In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:
  • A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
  • A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
  • Stock-based long-term incentives
  • Award-winning time-off plans
  • Flexible work models, including remote and hybrid work arrangements, where possible


Apply now and make a lasting impact with the Amgen team.

careers.amgen.com

In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.

Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.

About Amgen Inc

Amgen is a biotechnology company that develops and manufactures human therapeutics for various illnesses and diseases. The company is values-based and deeply rooted in science and innovation to transform new ideas and discoveries into medicines for patients with serious diseases. They offer products for treating illness in the areas of oncology/hematology, cardiovascular, inflammation, bone health, nephrology, and neuroscience.

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Join the dynamic team at Amgen Inc, a biotechnology pioneer dedicated to discovering, developing, and delivering innovative human therapeutics. At Amgen, we offer more than just job opportunities; we invite you to be part of a culture of leadership, diversity, and innovation.

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At Amgen Inc, you will collaborate with some of the brightest minds in the industry, engaging in work that brings real solutions to patients worldwide. Our commitment to your career growth is evident in our professional development and leadership training programs designed to nurture your potential.

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Amgen’s inclusive culture and commitment to diversity are integral to our success. We believe in empowering our employees with the skills and networking opportunities they need to thrive. Our team’s collaboration is the key to developing groundbreaking solutions.

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Amgen Inc offers a variety of career paths, from research and development to marketing and sales, providing near-limitless opportunities for advancement. Whether you are looking for a full-time position, an internship, or a leadership role, Amgen has a place for you. Our robust benefits package supports the well-being of our employees and their families, contributing to a fulfilling work-life balance.

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Learn more about Amgen Inc
Size
24,200 employees
Market Cap
$141.2 billion
Industry
Net Income
$7.2 billion
Founded
1980
5 Year Trend
+2.5%
Revenue
$25.4 billion
NASDAQ

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