Manager, Biostatistics
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Before you apply
Salary$128k – $159k
LocationUS-Remote
Work moderemote · United States
Typefull-time
SeniorityMid
Experience4+ yrs
Company size1,001–5,000 people
PostedOct 30, 2026 · 5d ago
Verified live1d ago
At a glanceSummarised by Seekless from the posting.
MS and 4 yrs of experience within Statistics, Biostatistics, or a related quantitative discipline or PhD in Statistics, Biostatistics, or a related quantitative discipline
Strong understanding of statistical principles and clinical trial methodology
Working knowledge of FDA, EMA, PMDA, ICH, and other applicable regulatory guidelines
Familiarity with CDISC standards, including SDTM and ADaM
Experience supporting the design, analysis, and reporting of clinical trials
Proficiency in SAS programming
Strong analytical, problem-solving, and communication skills
Ability to work effectively in a cross-functional team environment
Experience contributing to protocols, SAPs, CSRs, and regulatory submission documents
Must be able to exercise appropriate judgment as necessary
Requires a high level of initiative and independence
Experience with R is desirable
Oncology clinical development experience is preferred
Experience working with CROs and external vendors is desirable
Must be able to travel domestically and internationally as needed
Skills
SAS
R
Benefits
401(k)
Medical insurance
Dental insurance
Vision insurance
Life insurance
Disability insurance
Flexible PTO
Paid holidays
Paid sick leave
About the company
Sumitomo Pharma Co., Ltd., is a global pharmaceutical company based in Japan with operations in the U.S. (Sumitomo Pharma America, Inc.), focused on addressing patient needs in oncology, urology, women’s health, rare diseases, cell & gene therapies and CNS. With several marketed products and a diverse pipeline of early- to late-stage investigational assets, we aim to accelerate discovery, research, and development to bring novel therapies to patients sooner. For more information on SMPA, visit our website https://www.us.sumitomo-pharma.com or follow us on LinkedIn.
About the role
The Manager, Biostatistics (Oncology) provides statistical leadership and support for oncology clinical development programs from protocol development through clinical study reporting and regulatory submission. The individual serves as the lead statistician for one or more clinical studies and collaborates with cross-functional teams including Clinical Development, Statistical Programming, Data Management, Clinical Operations, Medical Writing, Regulatory Affairs, and external partners to ensure the successful execution of clinical trials.
Key Responsibilities
· Serve as lead statistician for one or more oncology clinical studies.
· Provide statistical input into study design, endpoint selection, sample size determination, randomization methodology, and analysis strategy.
· Contribute to the development and review of clinical study protocols.
· Author and review Statistical Analysis Plans (SAPs).
· Collaborate with Statistical Programming in the development and review of analysis datasets, tables, listings, and figures (TLFs).
· Review statistical outputs and ensure the quality, consistency, and accuracy of study deliverables.
· Interpret study results and communicate findings to multidisciplinary project teams.
· Contribute to the preparation of Clinical Study Reports (CSRs), abstracts, publications, and regulatory documents.
· Support regulatory submissions and responses to health authorities.
· Collaborate with CRO statisticians and programming teams to ensure timely and high-quality deliverables.
· Ensure compliance with regulatory requirements, company procedures, and industry standards.
· Participate in departmental initiatives to improve statistical processes and standards.
· Provide technical guidance and mentoring to junior statisticians as needed.
Professional Experience / Qualifications
· MS and 4 yrs of experience within in Statistics, Biostatistics, or a related quantitative discipline or PhD in Statistics, Biostatistics, or a related quantitative discipline.
· Strong understanding of statistical principles and clinical trial methodology.
· Working knowledge of FDA, EMA, PMDA, ICH, and other applicable regulatory guidelines.
· Familiarity with CDISC standards, including SDTM and ADaM.
· Experience supporting the design, analysis, and reporting of clinical trials.
· Proficiency in SAS programming; experience with R is desirable.
· Strong analytical, problem-solving, and communication skills.
· Ability to work effectively in a cross-functional team environment.
· Experience contributing to protocols, SAPs, CSRs, and regulatory submission documents.
Nice to have
· Oncology clinical development experience is preferred.
· Experience working with CROs and external vendors is desirable.
Competencies
· Scientific rigor and strong attention to detail.
· Effective written and verbal communication skills.
· Ability to communicate statistical concepts to both technical and non-technical audiences.
· Strong organizational and project management skills.
· Ability to manage multiple priorities in a fast-paced development environment.
· Commitment to quality, innovation, and continuous improvement.
Travel Requirements:
Primarily remote role with periodic on-site meetings in office. Must be able to travel domestically and internationally as needed.
Mental/Physical Requirements:
Fast-paced environment handling multiple demands is involved. Must be able to exercise appropriate judgment as necessary. Requires a high level of initiative and independence. Excellent written and oral communication skills required. Requires ability to use a personal computer for extended periods of time.
Benefits
The base salary range for this role is
$127,500.00 - $159,400.00
Base salary is part of our total rewards package which also includes the opportunity for merit-based salary increases, short incentive plan participation, eligibility for our 401(k) plan, medical, dental, vision, life and disability insurances and leaves provided in line with your work state. Our robust time-off policy includes flexible paid time off, 11 paid holidays plus additional time off for a shut-down period during the last week of December, 80 hours of paid sick time upon hire and each year thereafter. Total compensation, including base salary to be offered, will depend on elements unique to each candidate, including candidate experience, skills, education and other factors permitted by law.
Legal
Disclaimer: The above statements are intended to describe the general nature and level of work being performed by people assigned to this classification. They are not to be construed as an exhaustive list of all responsibilities, duties, and skills required of personnel so classified. All personnel may be required to perform duties outside of their normal responsibilities from time to time, as needed.
Confidential Data: All information (written, verbal, electronic, etc.) that an employee encounters is considered confidential, in accordance with applicable law.
Compliance: Achieve and maintain Compliance with all applicable regulatory, legal and operational rules and procedures, by ensuring that all plans and activities for and on behalf of Sumitomo Pharma America (SMPA) and affiliates are carried out with the “best” industry practices and the highest ethical standards.
It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
Drug Screening Requirements
Applicants for sales/field, manufacturing, or other designated roles will be required to submit to a pre-employment drug test.
Sumitomo Pharma America (SMPA) is an Equal Employment Opportunity (EEO) employer
Qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.
Sumitomo Pharma America (SMPA) endeavors to make its application process accessible to all. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process, please contact SMPA at [email protected]. This contact information is for accommodation requests only and cannot be used to inquire about the status of applications.