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TechData Service Company LLC

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Remote Biostatistician (Phase II/Oncology)

Warren, NJ · Remote

$90 - $110/hr

Biotech Position Summary: - 10+ years of biostatistics experience , with extensive oncology ... Statistical Analysis Plans (SAPs), define derived variables, and provide specifications to ...

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Danaher

Business Insights Analyst

Indianapolis, IN · On-site +1

Experience in Life Sciences, MedTech, Diagnostics, biotechnology or pharmaceutical organization ... We recognize the benefits of flexible, remote working arrangements for eligible roles and are ...

Horizontal Talent

Product Analyst

Minneapolis, MN · On-site +1

... this remote role, you will lead product strategy, roadmap planning, and cross-functional ... Experience in pharma or biotech, especially with cellular therapy market knowledge. * Familiarity ...

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How much do remote biotech analyst jobs pay per year?

As of Aug 24, 2026, the average yearly pay for remote biotech analyst in the United States is $73,261.00, according to ZipRecruiter salary data. Most workers in this role earn between $52,500.00 and $87,000.00 per year, depending on experience, location, and employer.

What is a remote biotech analyst?

Remote Biotech Analysts are professionals who analyze data, trends, and research in the biotechnology sector while working from a location outside of a traditional office, typically from home. They assess scientific advancements, company reports, and market developments to provide insights for investors, companies, or research institutions. Their work often involves reviewing clinical trial results, evaluating new technologies, and monitoring regulatory changes. Remote Biotech Analysts use digital communication tools to collaborate with colleagues and clients, making their expertise accessible regardless of location.

How do remote biotech analysts typically collaborate with laboratory teams and other stakeholders while working offsite?

Remote Biotech Analysts frequently use digital communication tools such as video conferencing, project management platforms, and secure data-sharing systems to stay connected with laboratory teams and other stakeholders. They participate in virtual meetings to discuss project updates, analyze data, and provide recommendations. Building strong communication habits and proactively scheduling check-ins are essential for overcoming the challenge of not being physically present. Additionally, clear documentation and timely reporting help ensure alignment and project success, making collaboration seamless despite the remote nature of the role.

What are the key skills and qualifications needed to thrive as a remote biotech analyst, and why are they important?

To thrive as a Remote Biotech Analyst, you need a strong background in biology or biotechnology, data analysis, and research methodologies, typically supported by a relevant degree. Familiarity with bioinformatics software, statistical tools like R or Python, and experience using databases such as PubMed are commonly required. Strong attention to detail, critical thinking, and effective written communication are vital soft skills for analyzing complex data and presenting findings clearly. These competencies are crucial for delivering accurate insights and supporting data-driven decisions in biotech organizations operating remotely.
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Remote Biotech Analyst jobs near you
Infographic showing various Remote Biotech Analyst job openings in the United States as of August 2026, with employment types broken down into 89% Full Time, 5% Part Time, and 6% Contract. Highlights an 80% Physical, 9% Hybrid, and 11% Remote job distribution, with an average salary of $73,261 per year, or $35.2 per hour.

Remote Biostatistician (Phase II/Oncology)

TechData Service Company LLC

Warren, NJ • Remote

$90 - $110/hr

Contractor

Medical, Dental, Life, Retirement, PTO

Posted 3 days ago

New

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Job description

Job Type: Contract
Length: 1 year (renewable)
Pay Rate: $90 - $110/hr.
Location: Remote (United States)
Company: Biotech


Position Summary:

-10+ years of biostatistics experience, with extensive oncology clinical trial experience
-Strong hands-on experience supporting Phase 2/3 studies, including protocol, SAP, TLFs, data review, and study deliverables
-Experience working cross-functionally with clinical, data management, programming, and medical teams
-Experience overseeing CRO statistical and programming activities
-Prostate cancer experience would be highly preferred


Key Responsibilities:

- Partner with Medical Directors, Clinical Scientists, Regulatory Affairs, Statistical Programming, Data Management, Medical Writing, and other colleagues to design clinical trials and frame statistical approaches to key drug-development questions.

- Contribute to or lead the development of study protocols, including sample size calculations and statistical methodology sections.

- Author Statistical Analysis Plans (SAPs), define derived variables, and provide specifications to programming teams.

- Perform or oversee statistical analyses according to the SAP; review Tables, Figures, and Listings (TFLs); and contribute to Clinical Study Reports (CSRs).

- Provide statistical insight into the interpretation and discussion of study results.

- Support regulatory interactions (e.g., analysis plans, briefing documents, advisory committee materials) and respond to agency questions.

- Participate in or lead post-hoc analyses, exploratory analyses, and evidence-generation activities (including Phase IV or real-world evidence studies, as applicable).

- Promote statistical thinking across the organization through training, consultation, and collaboration.

- Stay current with evolving statistical methodologies, regulatory guidance, and industry best practices; evaluate and apply innovative approaches when appropriate.

- Mentor more junior statisticians and contribute to process improvement and departmental initiatives.


Qualifications:

Required:

- PhD or equivalent in Statistics, Biostatistics, or a closely related field with relevant pharmaceutical/biotech experience, **or**

- MS in Statistics/Biostatistics with substantial industry experience (typically 10+ years depending on level).

- Solid understanding of clinical trial design, analysis, and interpretation in a regulated environment.

- Proficiency with statistical software (SAS required; R highly preferred; experience with other tools such as Python a plus).

- Strong knowledge of regulatory guidelines (FDA, EMA) and ICH standards related to statistical practice.

- Excellent written and verbal communication skills, with the ability to explain complex statistical concepts to both technical and non-technical audiences.

- Proven ability to work effectively in cross-functional, matrixed teams in a remote environment.

Company Description

https://quantive.bio/