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Remote Biostatistician Pharmaceutical Jobs (NOW HIRING)

System One

Biostatistician

Jersey City, NJ · Remote

$60 - $65/hr

Jersey City, NJ 07302 (Remote) Schedule: 24 hours/week (Choose: 9:00AM - 5:00PM) Compensation: $60 ... Experience supporting clinical studies in the medical device, biotechnology, or pharmaceutical ...

System One

Biostatistician

Jersey City, NJ · Remote

$60 - $65/hr

Jersey City, NJ 07302 (Remote) Schedule: 24 hours/week (Choose: 9:00AM - 5:00PM) Compensation: $60 ... Experience supporting clinical studies in the medical device, biotechnology, or pharmaceutical ...

System One

Biostatistician

Jersey City, NJ · Remote

$60 - $65/hr

Jersey City, NJ 07302 (Remote) Schedule: 24 hours/week (Choose: 9:00AM - 5:00PM) Compensation: $60 ... Experience supporting clinical studies in the medical device, biotechnology, or pharmaceutical ...

System One

Biostatistician

Jersey City, NJ · Remote

$60 - $65/hr

Jersey City, NJ 07302 (Remote) Schedule: 24 hours/week (Choose: 9:00AM - 5:00PM) Compensation: $60 ... Experience supporting clinical studies in the medical device, biotechnology, or pharmaceutical ...

System One

Biostatistician

Jersey City, NJ · Remote

$60 - $65/hr

Jersey City, NJ 07302 (Remote) Schedule: 24 hours/week (Choose: 9:00AM - 5:00PM) Compensation: $60 ... Experience supporting clinical studies in the medical device, biotechnology, or pharmaceutical ...

System One

Biostatistician

Jersey City, NJ · Remote

$60 - $65/hr

Jersey City, NJ 07302 (Remote) Schedule: 24 hours/week (Choose: 9:00AM - 5:00PM) Compensation: $60 ... Experience supporting clinical studies in the medical device, biotechnology, or pharmaceutical ...

System One

Biostatistician

Jersey City, NJ · Remote

$60 - $65/hr

Jersey City, NJ 07302 (Remote) Schedule: 24 hours/week (Choose: 9:00AM - 5:00PM) Compensation: $60 ... Experience supporting clinical studies in the medical device, biotechnology, or pharmaceutical ...

System One

Biostatistician

Jersey City, NJ · Remote

$60 - $65/hr

Jersey City, NJ 07302 (Remote) Schedule: 24 hours/week (Choose: 9:00AM - 5:00PM) Compensation: $60 ... Experience supporting clinical studies in the medical device, biotechnology, or pharmaceutical ...

System One

Biostatistician

Jersey City, NJ · Remote

$60 - $65/hr

Jersey City, NJ 07302 (Remote) Schedule: 24 hours/week (Choose: 9:00AM - 5:00PM) Compensation: $60 ... Experience supporting clinical studies in the medical device, biotechnology, or pharmaceutical ...

Biogen

Sr. Principal Biostatistician

$134K - $179K/yr

... pharmaceutical/biotech industry. Thorough understanding of statistical principles and clinical ... Although we are open to Remote candidates, the strong preference would be to have a Hybrid presence ...

Biogen

Sr. Principal Biostatistician

$134K - $179K/yr

... the pharmaceutical/biotech industry. • Thorough understanding of statistical principles and ... Although we are open to Remote candidates, the strong preference would be to have a Hybrid presence ...

Ultragenyx Pharmaceutical

Director, Biostatistics

OR · On-site +1

Remote: Officially documented as working full-time from home, with travel to Ultragenyx's offices ... pharmaceutical industry * Experienced in NDA / BLA / MAA activities as a key contributor from ...

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How much do remote biostatistician pharmaceutical jobs pay per hour?

As of Aug 26, 2026, the average hourly pay for remote biostatistician pharmaceutical in the United States is $57.55, according to ZipRecruiter salary data. Most workers in this role earn between $40.62 and $64.42 per hour, depending on experience, location, and employer.

What is a remote biostatistician in the pharmaceutical industry?

Remote biostatisticians in the pharmaceutical industry are professionals who apply statistical methods to analyze data from clinical trials and other research studies, while working from a location outside of a traditional office setting. They collaborate with research teams to design experiments, interpret study results, and ensure compliance with regulatory standards. Their work is critical for assessing the safety and efficacy of new drugs and medical treatments. By working remotely, they use digital tools to communicate, manage data, and contribute to the drug development process from virtually anywhere.

How does a remote biostatistician in the pharmaceutical industry typically collaborate with clinical research teams?

As a remote biostatistician in the pharmaceutical industry, you will regularly collaborate with cross-functional teams, including clinical researchers, data managers, and regulatory specialists. Communication often happens via video calls, shared platforms, and project management tools to ensure that statistical analyses align with study protocols and regulatory requirements. You may be responsible for providing statistical input during study design, reviewing data quality, and presenting findings to both technical and non-technical stakeholders. Building strong virtual relationships and maintaining clear documentation are key to overcoming the challenges of remote collaboration.

What are the key skills and qualifications needed to thrive as a remote biostatistician in the pharmaceutical industry?

A Remote Biostatistician in the pharmaceutical industry requires strong statistical analysis skills, proficiency in biostatistics, and a degree in statistics, mathematics, or a related field, often with experience in clinical trials. Expertise with statistical software such as SAS, R, and familiarity with regulatory guidelines like FDA or ICH E9 is typically expected. Excellent problem-solving, attention to detail, and clear written and verbal communication are essential soft skills for effective collaboration and reporting. These competencies ensure the accurate interpretation of clinical data, regulatory compliance, and impactful contributions to drug development from a remote setting.

What is the difference between Remote Biostatistician Pharmaceutical vs Remote Biostatistician Clinical Research?

AspectRemote Biostatistician PharmaceuticalRemote Biostatistician Clinical Research
CredentialsMaster's or PhD in Biostatistics, Statistics, or related fieldMaster's or PhD in Biostatistics, Statistics, or related field
Work EnvironmentPharmaceutical companies, biotech firms, CROsAcademic institutions, CROs, healthcare organizations
Industry UsageDrug development, regulatory submissionsClinical trials, patient studies
Common Search IntentPharmaceutical industry roles, drug trialsClinical trial analysis, patient data

Remote Biostatistician Pharmaceutical roles focus on drug development and regulatory submissions within the pharmaceutical industry, requiring industry-specific knowledge. In contrast, Remote Biostatistician Clinical Research positions often involve analyzing clinical trial data across various healthcare settings. Both roles require similar credentials but differ in industry focus and work environment.

More about Remote Biostatistician Pharmaceutical jobs

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The top searched job categories for Remote Biostatistician Pharmaceutical jobs are:

Remote Biostatistician Pharmaceutical jobs near you
Infographic showing various Remote Biostatistician Pharmaceutical job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, 1% Temporary, 3% Contract, and 1% Nights. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution, with an average salary of $119,702 per year, or $57.5 per hour.

Remote Biostatistician (Phase II/Oncology)

Warren, NJ • Remote

TechData Service Company LLC
Biotechnology Research and Development • 51 - 200 employees
Learn more about TechData Service Company LLCexternal

$90 - $110/hr

Contractor

Medical, Dental, Life, Retirement, PTO

Posted 5 days ago

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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/