Top 7 Biostatistician Jobs in Carlstadt Nj

Clinical Services: Senior Biostatistician
Canfield Scientific —Parsippany-Troy Hills, NJ
- $120,000 - $160,000 a year
- Master's degree
- Analysis skills
- Doctor of Philosophy
- Paid holidays
- Health insurance
Principal, Biostatistician
Roivant Sciences —New York, NY
- $130,000 - $220,000 a year
- Full-time
- Senior level
- Commercial
Clinical Assistant Professor | Biostatistician
New York University —New York, NY
- $120,000 - $180,000 a year
- University
- Doctor of Philosophy
- Mentoring
Biostatistician - Med Faculty Open Rank
The City University of New York (CUNY) —New York, NY
- $80,982 - $169,995 a year
- Bachelor of Science
- Analysis skills
- University
- Paid parental leave
- Health insurance

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Clinical Services: Senior Biostatistician

Canfield Scientific -
Parsippany-Troy Hills, NJ

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Job Details

$120,000 - $160,000 a year

Benefits

Paid holidays
Health insurance
Dental insurance
Paid time off
Vision insurance
401(k) matching

Qualifications

Data integrity assurance
Technical writing for researchers
Statistics
Medical writing
Clinical study protocols and reports
Content creation for technical audiences
Statistics
Biostatistics-based research
Medical statistical report preparation
SAS
SAS language
Data integrity and documentation
ICH guidelines
Statistics research
Quality control
Clinical program data analysis
Compliance documentation
Managing projects
Regulatory compliance analysis
Clinical data analysis
Technical Proficiency
Scientific reports

Full Job Description

We are seeking a skilled and motivated Senior Biostatistician to join our fast-moving, collaborative environment focused on medical imaging and dermatology-based clinical development. In this role, you will support clinical studies through statistical planning, analysis, and reporting activities. The position requires strong technical expertise in statistics and SAS programming, with the ability to independently develop Statistical Analysis Plans (SAPs), execute and validate statistical analyses, and prepare statistical components of clinical study reports (CSRs). The right candidate can translate statistical outputs into clinically meaningful interpretations and communicate findings clearly to both technical and non-technical audiences.

Job Description

Independently author Statistical Analysis Plans (SAPs), including definition of analysis populations, endpoints, statistical methods, missing data handling, and sensitivity analyses
Provide statistical input into study protocols, including endpoint definition, sample size considerations, and methodological recommendations
Independently develop, validate, and maintain SAS programs for analysis datasets, tables, listings, and figures (TLFs) in accordance with SAPs
Perform statistical analyses aligned with SAPs and study objectives, ensuring accuracy, reproducibility, and compliance with regulatory expectations
Prepare statistical sections of clinical study reports (CSRs), including interpretation of results
Ensure analyses adhere to ICH and FDA guidance
Collaborate cross-functionally with clinical, regulatory, data management, and medical writing teams to support study deliverables

Core Requirements

Master’s degree in Biostatistics, Statistics, Mathematics or closely related quantitative discipline with at least 4 years of clinical research within a regulated environment (pharmaceutical, biotechnology, CRO, or medical device industry) or PhD with at least 2 years of relevant experience
Demonstrated experience independently authoring Statistical Analysis Plans (SAPs), contributing to clinical study reports and regulatory documentation
Proficiency in SAS, including validated code development, QC, and production of regulatory-grade TLFs
Solid understanding of statistical methodology for clinical trials, including analysis population definitions, endpoint types, missing data, and multiplicity considerations
Ability to communicate statistical results within the clinical study context
Working knowledge of ICH E9/E9(R1) and FDA regulatory expectations
Strong analytical skills with high attention to data integrity, reproducibility, and traceability
Ability to manage projects or analysis within established timelines

Desired

Experience with medical imaging or dermatology clinical studies
Exposure to regulatory submission processes
Experience contributing to peer-reviewed publications

Canfield Scientific, Inc. is a core imaging lab providing custom photographic systems, image monitoring, and centralized analysis services for the pharmaceutical, biotechnology and cosmetics industries supporting global clinical trials providing primary endpoint data and supporting documentation. Canfield offers comprehensive benefits to its eligible full-time employees. These include paid days off, medical, dental, and vision insurance, may be eligible for a discretionary bonus, and a 401(k) plan with employer match (currently set at 50%). The anticipated salary range for the position is $120,000.00-$160,000.00 annually. This is dependent upon consideration of multiple factors when determining a base salary such as a candidate’s experience, education, and current market conditions. If the role is eligible for full benefits, it will be discussed with you during the interview process. Canfield's imaging equipment leads the industry providing high-quality, registered, reproducible clinical images. This, together with proactive clinical image monitoring and a world class quality assurance regimen, sets the gold standard in image quality for clinical studies.

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biostatistician jobs in carlstadt nj

Clinical Services: Senior Biostatistician

Principal, Biostatistician

Clinical Assistant Professor | Biostatistician

Biostatistician - Med Faculty Open Rank

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