Top 316 Data manager/statistician Jobs

Associate Director, Biostatistics (Late Stage)
Daiichi Sankyo, Inc. —Basking Ridge, NJ
- $175,440 - $263,160 a year
- 5 years
- Office
- Master's degree
SAS programmer
JN Data Resolution LLC —Florham Park, NJ
- $82,000 a year
- Full-time
- Computer Science
- Office
- Master's degree
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SQL Programmer
VA Boston Healthcare System —Boston, MA
- Full-time
- Background check
- SQL
- Bachelor's degree
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Senior Manager
BMS —Princeton, NJ
- $164,110 - $198,862 a year
- Email
- Hybrid work
- Computer Science
- Master's degree
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- Paid holidays
- Disability insurance
Manager I, Engineering - Experiments
Datadog —New York, NY
- $192,000 - $240,000 a year
- Mid-level
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- Recruiting
- Employee stock purchase plan
- Health insurance
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6d
Director, Biostatistics Hematology
BMS —Princeton, NJ
- $216,570 - $262,434 a year
- Email
- Hybrid work
- Writing skills
- Doctor of Philosophy
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Associate Director, Biostatistics
Genmab —Princeton, NJ
- $156,880 - $235,320 a year
- Online Application
- Master's degree
- Databases
- Doctor of Philosophy
- Commuter assistance
- Paid parental leave
Director, Biostatistics
BMS —Madison, NJ
- $218,740 - $265,060 a year
- Email
- Hybrid work
- Writing skills
- Doctor of Philosophy
- Travel
- Paid holidays
- Disability insurance
Senior Biostatistician II
Vertex Pharmaceuticals —Boston, MA
- $132,200 - $198,200 a year
- Full-time
- Hybrid work
- 3 years
- Master's degree
- Doctor of Philosophy
- Loan repayment program
- Dental insurance
Clinical Data Manager
MM Infotech —Remote
- Full-time
- Remote
- Bachelor of Science
- Mid-level
- 3 years
Manager, Clinical Data Management
Immunocore —Radnor, PA
- $107,250 - $178,750 a year
- Full-time
- 5 years
- Bachelor of Science
- Writing skills
Mathematical Statistician (Data Scientist) - Direct Hire
US Internal Revenue Service —Anchorage, AK
- $74,678 - $172,980 a year
- Online Application
- Hybrid work
- Background check
- 18 years or older
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10d
Clinical Research Project Manager (2+ years Clinical Trials Exp. Required)
Biotrial, Inc. —Newark, NJ
- $90,000 - $120,000 a year
- Full-time
- Bachelor of Science
- Writing skills
- Mid-level
- Health insurance
- Dental insurance
Quick Apply
12d
Data Scientist I
Generate Biomedicines —Somerville, MA
- $140,000 - $170,000 a year
- SQL
- Doctor of Philosophy
- Entry level
10d
Lab Data Manager I/II
Fred Hutchinson Cancer Center —Seattle, WA
- $80,475 - $133,058 a year
- Full-time
- Mid-level
- 3 years
- Master's degree
- Paid parental leave
- Paid holidays
Project Manager B: Protocol Development, Clinical Statistics and Data Analyses
University of Pennsylvania —Philadelphia, PA
- $66,000 - $81,441 a year
- Full-time
- Background check
- Management
- Mid-level
- Health insurance
- Dental insurance
Strategic Account Manager
Natera —Philadelphia, PA
- $190,000 - $220,000 a year
- Remote
- Up to 50% travel
- Mid-level
- 3 years
- Commuter assistance
- Health insurance
Senior Director – Real World Data (RWD) Architect - Engineer
Eli Lilly —Indianapolis, IN
- $169,500 - $248,600 a year
- Full-time
- DevOps
- HIPAA
- English
- Health insurance
- Dental insurance
3d
Data Manager and Statistical Analyst
University at Buffalo —Buffalo, NY
- $63,000 - $75,000 a year
- Full-time
- Computer Science
- System design
- Mid-level
- Health insurance
- Loan forgiveness
Data Science Manager, Tapestry
Loon —Mountain View, CA
- $207,000 - $304,000 a year
- Full-time
- Hybrid work
- 5 years
- Master's degree
- SQL
- Health insurance
- Dental insurance
3d

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Associate Director, Biostatistics (Late Stage)

Daiichi Sankyo, Inc. -
Basking Ridge, NJ

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Job Details

$175,440 - $263,160 a year

Qualifications

Master's degree
Pharmaceutical company experience

Full Job Description

Job Title:
Associate Director, Biostatistics (Late Stage)

Job Requisition ID:
1282

Posting Start Date:
4/2/26

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

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