Jobs at Daiichi Sankyo

Positions 2,118

Daiichi Sankyo Co., Ltd. is a leading global biopharmaceutical company headquartered in Tokyo, Japan. Since its merger with Sankyo in 2005, it has expanded its portfolio to include cardiovascular, oncology, and central nervous system therapies. The company also invests heavily in digital health, data analytics, and AI‑driven drug discovery, positioning it as a key player where biotechnology meets technology.

Candidates can find roles ranging from medicinal chemistry and clinical data management to software engineering and IT infrastructure. The 214 open positions cover product development, regulatory affairs, data science, cybersecurity, and software services that support clinical trial automation. Applicants can expect rigorous technical assessments, collaborative cross‑functional teams, and opportunities to work on global pipeline projects.

Job Transparency provides real‑time salary ranges and employee sentiment scores for each Daiichi Sankyo listing. By comparing compensation data with industry benchmarks and reading candid reviews, you can evaluate whether a role aligns with your career goals and compensation expectations before submitting an application.

Sr. Study Manager

Company: Daiichi Sankyo

Location: Other US Location

Posted Apr 19, 2023

Daiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging world-class science and technology. The company is primarily focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders. In an effort to build a strong candidate pipeline for future job openings, Daiichi Sankyo is accepting applications for (Sr. Study Manager) professionals. The incumbent will be responsible for ensuring the delivery execution of clinical studies in one or more geographic regions, in adherence to Good Clinical Practices (GCPs), appropriate Standard Operating Procedures (SOPs), Food and Drug Administration (FDA) regulations/EU Directive, and International Conference on Harmonization (ICH) guidelines. The Senior Clinical Study Manager will have routine interaction with key internal and external stakeholders communicating project status, escalating issues, and troubleshooting routine inquiries. The role is primarily a tactical study delivery role, reporting into an Associate Director (or above) responsible for Operational Study Strategy. The Senior Clinical Study Manager will have primary accountability for operational study level time, cost, and quality deliverables. They will lead the development of the clinical study plan, create the cross-functional Clinical Study Oversight Plan (CSOP), and provide operational input into study protocol profiles, final protocols and amendments. They will also lead document review & coordination for the protocol and amendments, and lead the CRO and vendor selection process in collaboration with the study team and outsourcing procurement management.

Director, Change Management. Change & Enablement

Company: Daiichi Sankyo

Location: Other US Location

Posted May 14, 2023

Daiichi Sankyo Group is dedicated to creating innovative pharmaceutical therapies to improve healthcare standards and address unmet medical needs. The company is focused on providing novel therapies in oncology and other research areas.

Associate Director, Biostatistics

Company: Daiichi Sankyo

Location: Other US Location

Posted May 12, 2023

The text describes a position at Daiichi Sankyo Group, a company with a legacy of innovation in pharmaceutical therapies. The role involves leading complex studies in drug development, providing input to multiple aspects of the development plan, and improving the harmonization and efficiency of drug development. The position requires a PhD in statistics or biostatistics, 5 or more years of relevant experience in the pharmaceutical industry, and strong statistical skills.

Director, Global Project Management & Leadership (Drug Development)

Company: Daiichi Sankyo

Location: Other US Location

Posted Apr 19, 2023

This position is responsible for providing project management, drug development expertise to Global Project Teams including strategic development and execution of an integrated product development plan. The position is accountable for partnering with the Global Team leader as the Project Management lead on drug development projects. The position can be assigned to any therapeutic area and work on projects at any stage of development. As a member of the GMP&L function, this position is also accountable for supporting divisional and departmental level objectives and may also lead a non-project initiative in support of these objectives. This position will report to the Sr Director, Group Leader, GPM&L.

Sr. Study Manager

Company: Daiichi Sankyo

Location: Other US Location

Posted May 15, 2023

Daiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging world-class science and technology. With more than 100 years of scientific expertise and a presence in more than 20 countries, Daiichi Sankyo and its 15,000 employees around the world draw upon a rich legacy of innovation and a robust pipeline of promising new medicines to help people. Under the Group's 2025 Vision to become a 'Global Pharma Innovator with Competitive Advantage in Oncology,' Daiichi Sankyo is primarily focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders. The text input is a job description for a Senior Clinical Study Manager position at Daiichi Sankyo Group.

Manager, BioSample Operations

Company: Daiichi Sankyo

Location: Other US Location

Posted May 16, 2023

Daiichi Sankyo Group, a global pharmaceutical company with over 100 years of experience, is dedicated to creating innovative therapies for diverse medical needs. The Manager, Bio-Sample Operations, is responsible for overseeing the lifecycle of biomarker samples in clinical trials, ensuring proper handling, tracking, and storage. This role involves collaboration with various cross-functional teams, including Clinical Biomarker, Companion Diagnostics, and Clinical Study Teams. Key responsibilities include near real-time tracking of samples, managing sample lifecycle activities, and supporting data reconciliation and resolution of sample-related issues. The role also involves process documentation and improvement, people management, and resource planning. Successful candidates should have a Bachelor's Degree in a Life Sciences field, minimum 4 years of pharmaceutical or biotechnology drug development experience, and 2 or more years of bio-sample handling experience. Excellent organizational and communication skills, advanced Excel knowledge, and the ability to manage multiple priorities are required.

Associate Director, Biostatistics

Company: Daiichi Sankyo

Location: Other US Location

Posted May 15, 2023

The position involves leading complex studies in study design, statistical analysis, and interpretation of results with minimal supervision. It contributes to drug development plans, documents submission to Health Authorities, and guides CRO programmers and statisticians. The role involves protocol development, CRF review, SAP development, statistical analysis, results interpretation, and CSR input. It provides input to drug development strategy and CRO/vendor oversight. The position requires a PhD in statistics or biostatistics and 5 or more years of relevant experience in the pharmaceutical industry.

Manager, Data Management

Company: Daiichi Sankyo

Location: Other US Location

Posted May 08, 2023

None Found

Senior Analyst, Statistical Programming

Company: Daiichi Sankyo

Location: Other US Location

Posted Apr 21, 2023

The purpose of this job is to support quality assurance of statistical vendor deliverables, including performing programmatic review of analysis datasets and Table, Listing, and Figures (TLFs) generated by vendor, ensuring deliverable quality, and helping to expedite the preparation of regulatory submission. It will also to support statistical analysis during submissions and post-submission regulatory response period by independently developing and/or validating analysis datasets, and TLFs.

Dir HR Systems & People Analytics

Company: Daiichi Sankyo

Location: Other US Location

Posted May 16, 2023

The text describes a role in HR systems and technology, focusing on designing, deploying, and managing HR technology applications, as well as leading a team and providing strategic oversight. The role also involves project management, ensuring system compliance, and staying updated on industry trends.

Associate Director, Global Brand Strategy

Company: Daiichi Sankyo

Location: Other US Location

Posted May 14, 2023

Daiichi Sankyo Group is dedicated to creating innovative pharmaceutical therapies to improve standards of care and address unmet medical needs globally. The Global Brand Associate Director is responsible for supporting the development and execution of strategic planning and commercialization efforts globally.

Manager, Market Access Marketing and Strategy

Company: Daiichi Sankyo

Location: Other US Location

Posted Apr 18, 2023

Daiichi Sankyo Group is dedicated to creating and supplying innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging world-class science and technology. The company is primarily focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders.

Frequently Asked Questions

What’s it like to work at Daiichi Sankyo?
Employees describe a culture that rewards scientific curiosity and cross‑disciplinary collaboration. Teams are structured around project‑centric squads that include chemists, data scientists, and IT specialists, promoting rapid prototyping and iterative learning. The company offers global mobility programs, allowing staff to rotate between Japan, the U.S., and Europe, and provides continuous learning resources such as internal MOOCs on regulatory science and AI tools. Work‑life balance initiatives, including flexible hours and remote work options for eligible roles, help maintain employee well‑being while pursuing ambitious research goals.
What types of positions are available at Daiichi Sankyo?
The current 214 openings span several functional areas: 1) Research & Development – medicinal chemistry, pharmacology, and clinical data science; 2) Clinical Operations – data management, clinical project management, and regulatory affairs; 3) Information Technology – software engineering, DevOps, cybersecurity, and infrastructure support; 4) Manufacturing & Quality – GMP manufacturing, quality assurance, and process engineering; 5) Corporate – finance, human resources, marketing, and business development. Each role requires a blend of scientific expertise and technical proficiency, with many positions offering opportunities to contribute to global drug development pipelines.
How can I stand out as an applicant for Daiichi Sankyo?
Tailor your resume to highlight specific biotech or tech experience, such as experience with high‑throughput screening, machine‑learning models for drug discovery, or clinical data warehouse implementation. Quantify achievements (e.g., reduced data processing time by 30%) and include any relevant publications or patents. During interviews, demonstrate problem‑solving skills by discussing how you tackled regulatory challenges or optimized a clinical trial workflow. Show enthusiasm for the company’s focus on digital health by mentioning any projects involving AI or cloud analytics. Finally, engage with Daiichi Sankyo’s employee community on LinkedIn or the company’s career portal to learn about internal culture and current projects, then reference that knowledge in your cover letter.

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