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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 ... through training, consultation, and collaboration. - Stay current with evolving statistical ...

New

NNIT

Clinical Business Consultant

Davidson, NC · On-site +1

Experience working in or with regulated life sciences environments, such as pharmaceutical, biotech ... Experience with digital biomarkers, wearables, sensors, remote patient monitoring, decentralized ...

Teamwork Corporate

Supply Chain Consultant

We offer opportunities for continuous learning, a robust benefits package, remote work flexibility ... You have worked in or alongside pharma, biotech, or life sciences environments (preferred, not ...

synergy

New Business Development Manager

Dallas, TX · Remote

... Remote - National Territory) Travel: ~40-50% Overview Synergy Bioscience is a Contract Research, Development, Testing, and Consulting Organization (CRO) supporting pharmaceutical, biotechnology, and ...

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How much do biotech consultant remote jobs pay per hour?

As of Aug 23, 2026, the average hourly pay for biotech consultant remote in the United States is $49.72, according to ZipRecruiter salary data. Most workers in this role earn between $24.28 and $62.50 per hour, depending on experience, location, and employer.

What is a biotech consultant remote?

A Biotech Consultant Remote job involves providing expert advice to biotechnology companies, research organizations, or healthcare firms while working remotely. Consultants may specialize in regulatory compliance, product development, market strategy, or business operations. They analyze data, offer strategic insights, and help clients navigate industry challenges. This role typically requires a strong background in biotech, life sciences, or pharmaceuticals and excellent communication skills. Remote consultants use virtual tools to collaborate with teams and clients across different locations.

What does a biotech consultant remote do?

A typical day for a remote Biotech Consultant involves analyzing client data, developing strategic recommendations, and communicating findings via virtual meetings and reports. You may spend your time coordinating with clients, leading project teams, and staying up-to-date on industry trends and regulatory requirements. Flexible scheduling allows for independent, focused work but also requires strong time management to meet deadlines. Collaboration is often facilitated through digital platforms, enabling dynamic teamwork across different locations. This setup offers a stimulating mix of independent analysis and interactive client engagement.

What are the key skills and qualifications needed to thrive as a biotech consultant remote?

To thrive as a Biotech Consultant Remote, you need a solid background in biotechnology or life sciences, analytical problem-solving skills, and relevant consulting experience, ideally supported by a bachelor's or advanced degree. Familiarity with laboratory data analysis software, project management tools, and possibly certifications like PMP or Six Sigma is commonly expected. Exceptional communication, self-motivation, and the ability to manage client relationships virtually are crucial soft skills for remote work. These qualifications enable effective project delivery, client satisfaction, and seamless collaboration across dispersed teams in the biotech sector.

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Biotech Consultant Remote jobs near you
Infographic showing various Biotech Consultant Remote job openings in the United States as of August 2026, with employment types broken down into 50% Full Time, and 50% Contract. Highlights an 100% Remote job distribution, with an average salary of $103,425 per year, or $49.7 per hour.

Remote Biostatistician (Phase II/Oncology)

TechData Service Company LLC

Warren, NJ • Remote

$90 - $110/hr

Contractor

Medical, Dental, Life, Retirement, PTO

Posted 2 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/