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What is it like to work at Daiichi Sankyo?

Daiichi Sankyo is a global pharmaceutical company that values innovation, collaboration, and patient-centricity, fostering a culture of teamwork and mutual respect among its employees.

The company's structure is organized into various business units, including oncology, cardiovascular, and infectious diseases, allowing employees to work on projects that align with their interests and expertise. Daiichi Sankyo's global headquarters in Tokyo, Japan, and its research facilities in the United States and Europe, provide a dynamic and international work environment.

Working at Daiichi Sankyo may appeal to candidates who are passionate about developing innovative treatments for life-threatening diseases and are eager to contribute to a company that prioritizes patient needs and strives to make a positive impact on society.

What makes Daiichi Sankyo an attractive place to work?

Daiichi Sankyo is a global pharmaceutical company with a long history of innovation and commitment to improving patient outcomes, positioning itself as a leader in the industry. The company offers a dynamic work environment that fosters collaboration, creativity, and professional growth, with opportunities to work on cutting-edge projects and contribute to the development of new treatments. By joining Daiichi Sankyo, individuals can leverage their skills and expertise to make a meaningful impact in the field of healthcare and advance their careers in a stable and supportive organization.
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Infographic showing various Statistical Programmer job openings at Daiichi Sankyo in the United States as of July 2026, with employment types broken down into 98% Full Time, and 2% Contract. Highlights an 98% Physical, and 2% Hybrid job distribution.
Associate Director, Biostatistics (Late Stage)

Associate Director, Biostatistics (Late Stage)

Daiichi Sankyo, Inc.

Basking Ridge, NJ • On-site

$175K - $263K/yr

Other

Posted 26 days ago

Job description

At Daiichi Sankyo, we are united by a single purpose, to improve lives around the world through innovative medicines. With a legacy of innovation since 1899, a presence in more than 30 countries, and more than 19,000 employees, we are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases, and immune disorders. Guided by our 2030 vision to "be an innovative global healthcare company contributing to the sustainable development of society", we are shaping a healthier, more hopeful future for patients, their families, and society. Job Summary Position leads complex studies in study design, statistical analysis and interpretation of results with some supervision. This position contributes to specific aspects of drug development plans with minimal supervision and contributes to documents submitted to Health Authorities globally with some supervision. This position also guides contract research organization (CRO) programmers and statisticians in preparing analysis files and performing statistical analyses. Additionally, this position interacts with study teams, as well as statisticians and programmers at CROs. This position works under some supervision to solve complex study problems. Responsibilities Protocol Development, Case Report Form (CRF; review), Statistical Analysis Plan (SAP), Statistical Analysis, Results Interpretation, and clinical study report (CSR): Leads statistical activities for complex studies including study design, protocol development, CRF review, SAP development, analysis files development, statistical analysis accuracy validation, results interpretation and CSR input and review. Acts as main statistical contact for the assigned studies and projects. Provides guidance to study team on all aspects of statistical activities; collaborates closely with data manager to ensure high quality data. Drug Development Strategy: Provides input to multiple aspects of the development plan to ensure the study designs at each phase of the development are scientifically sound, can fulfill regulatory requirements and deliver the pre-specified product profile. CRO / Vendor Oversight: Review CRO/vendor proposal and budget. Establishes procedures through regular interaction, setting expectation on deliverables and timelines to guide CRO biostatistician and statistical programmers on complex studies. Ensures deliverables are accurate and delivered according to the timelines. Global Health Authority Interaction / Negotiation: Contributes to documents submitted to Health Authorities globally by providing input for the interaction or by writing the interaction document. May participate in meeting or teleconferences with Health Authorities Global BDO Strategy to Improve Drug Development: Primarily participates and may occasionally lead moderately complex initiatives, with some level of supervision, to improve the harmonization and efficiency of drug development which leads to cost savings and shortened timelines for the company. Qualifications Education Qualifications Master's Degree in statistics or biostatistics required PhD in statistics or biostatistics preferred Experience Qualifications 8+ Years of relevant experience in the pharmaceutical industry with a masters degree required 5+ Years of relevant experience in the pharmaceutical industry with a PhD preferred Travel Requirements Ability to travel up to 10% of the time. Daiichi Sankyo, Inc. is an equal opportunity/affirmative action employer. Qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, age, or any other characteristic protected by law. Salary Range: USD$175,440.00 - USD$263,160.00 Download Our Benefits Summary PDF

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