38 Results for

Biostatistics Jobs in Linden, NJ

Jobs

Basking Ridge, NJ13 days ago

$201,840–$302,760 Per Year
Full-time

Mentoring and Coaching Junior Statisticians: Mentoring the study level statisticians for the assigned projects to ensure optimal statistical handling and quality deliverables including Protocol Development, Statistical Analysis Plan (SAP), Statistical Analysis, Results Interpretation, and Clinical Study Report (CSR). Drug Development Strategy: Provides input to the clinical development plan to ensure the overall strategy can deliver the pre-specified product profile, is logical, scientifically sound, proposed studies have appropriate designs, efficacy and safety information to be collected meet regulatory agencies’ requirements for countries and regions the drug is to be submitted.

Basking Ridge, NJ13 days ago

$168,000–$252,000 Per Year
Full-time

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. 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.

Basking Ridge, NJ11 days ago

$271,500–$452,500 Per Year
Full-time

Provides regular status updates on projects, metrics and KPIs to Head of BDM and BDM LT External Vendor Oversight: Provides oversight of and is accountable for the quality/performance and budget, resources and timelines across the department and ensures timely delivery of high-quality deliverables at reasonable cost. This role also serves as a key member of the BDM leadership team, contributing to BDM broader organizational strategy, cross-functional decision-making, and the advancement of BDM objectives beyond the Biostatistics function.

Basking Ridge, NJ13 days ago

$157,920–$236,880 Per Year
Full-time

Master's Degree in Biostatistics, Data Science, Statistics, Applied Mathematics, Epidemiology, or related field plus 7 years of experience in epidemiologic methods and data analysis (pharmaceutical industry in safety or associated service provider experience is preferred) required PhD in Biostatistics, Data Science, Statistics, Applied Mathematics, Epidemiology, or related field plus 4 years of experience in epidemiologic methods and data analysis (pharmaceutical industry in safety or associated service provider experience is preferred) preferred. Provide data management of diverse data (e.g., real-world setting and clinical trial) to set up epidemiologic data sets for various approaches, quantitative epidemiologic data analysis, interpretation of results, visualization of results, and generate manuscripts to disseminate findings.

Basking Ridge, NJ13 days ago

$275,250–$458,750 Per Year
Full-time

The individual assuming this role may function as a key member of the Global Product Team in collaboration with Clinical Development, Regulatory, Project Management, Biostatistics, Pharmacology, and other departments to strategically manage benefit-risk throughout the lifecycle of the drug. Depending on the status of development of the compound, lead and medical-scientifically direct a team of physicians and scientists responsible for a compound/product including project-specific training and coaching of team members and review of team output cross-functionally.

Basking Ridge, NJ13 days ago

Develop and validate datasets and Tables, Listings, and Figures (TLFs) to ensure high-quality deliverables for pivotal studies, as well as Integrated Summary of Efficacy (ISE) and Integrated Summary of Safety (ISS) for oncology regulatory submissions. This role ensures the quality, consistency, and timeliness of deliverables supporting oncology regulatory submissions by guiding programming strategies, reviewing key outputs, and driving issue resolution.

Lawrenceville, NJ13 days ago

Full-time
Employee

Responsibilities:Data Analytics and ReportingBuild and continuously improve data analytics through supporting models that provide insights into efficiency, quality, stakeholder feedback, and key performance indicators to drive timely and informed decision making. The PV Analytics and Reporting Specialist, PV Analytics Center of Excellence applies a combination of life sciences strategy, leadership, and reporting/visualization experience to drive successful servicing of information needs across PS.

Raritan, NJ30+ days ago

Remote

Full-time

The Senior Scientist, Biostatistics will support the Oncology Therapeutic Area with a focus on: solid tumors or hematologic malignancies; cancer interception with the goal of developing products that interrupt the carcinogenic process; biomarkers that may help guide targeted, individualized use of our therapies; as well as safe and effective identification and treatment of early changes in the tumor microenvironment. Raritan, New Jersey, United States of America, San Diego, California, United States of America, Spring House, Pennsylvania, United States of America, Titusville, New Jersey, United States of America.

Bronx, New York27 days ago

Biostatistics faculty collaborate widely across the institution; teach in the medical and graduate educational programs; and lead and participate in biostatistics resources in the ICTR, Montefiore Einstein Comprehensive Cancer Center, Center for AIDS Research, Einstein Aging Study, and other research programs. The Division of Biostatistics in the Department of Epidemiology and Population Health includes more than 20 faculty members with active research programs in clinical trials methodology, statistical genetics and genomics, epidemiologic methods, machine learning, and analysis of real-world data.

Princeton, NJ30+ days ago

Contribute to the development and implementation of innovation in statistical methodology and trial design; perform simulations to assess various study design options and analysis approaches. Currently they are seeking an Associate Director of Biostatistics to support registration-directed clinical development programs and global regulatory submissions.

New York, NY22 days ago

$220,000–$240,000 Per Year

In collaboration with functional leads, ensure that the execution of clinical trials, (specifically data capture, cleaning) delivers quality and timely ongoing and final databases, develop strategies to minimize the cost of clinical trial execution in delivering quality clinical trial data and ensure that clinical trial systems used in the running of clinical trials are effectively linked to avoid conflicting information. Minimum 15 years of experience in leading biostatistics in clinical research (at various levels and in different capacities), including having built the biostatistics function and 5 years managing a biostatistical group working on all phases of clinical research and drug development.

Somerset, New Jersey19 days ago

$72,000–$72,000

Led by former FDA experts and industry experts, R&G US can provide end-to-end services in strategic planning, clinical trial design, statistical analysis, SAS programming, data management, medical writing, medical monitoring, pharmacovigilance, and Data Monitoring Committee services. R&G US's goal is to provide the best service to the clients and work as one team to lower costs, shorten development time, and increase the success probability of products.

Paramus, New Jersey30+ days ago

This role will lead key statistical activities across clinical trials and work closely with cross-functional teams, programmers, data management, and external partners to ensure high-quality statistical deliverables and timely execution. A growing pharmaceutical organization is seeking an experienced Biostatistics leader to support clinical development programs from protocol design through final study reporting, regulatory submissions, and post-study analysis.

Jersey City, NJ18 days ago

Remote

Full-time

Leads projects (all phases and even a program of studies) and smaller submissions, manages client meetings, CRMs, collaborates well with regulatory, PMs and sponsor. With a global footprint across four continents, MMS not only maintains an industry-leading customer satisfaction rating but also fosters a collaborative and inclusive work environment where employees can thrive.

Paramus, New Jersey17 days ago

Principal Statistics requires: SAS, ICH guidelines, CDISC data structures, FDA guidelines, SAP preparation, TFL shells, CRF review, database design review, edit check specifications, sample size calculation, analysis dataset validation, CRO oversight. Principal Statistics duties: Review protocol, understand study requirements, prepare statistical sections, design study elements including sample size calculation, analysis methods, study duration, etc.

Princeton, NJ13 days ago

Full-time

You will work closely with cross-functional teams, including clinical, regulatory, and international colleagues, to contribute to statistical analyses that inform decision-making across the clinical pipeline. It specializes in developing innovative cancer treatments using its established drug development platforms, focusing on bi-specific, multi-specific antibodies, and antibody-drug conjugates (ADCs).

Jersey City, NJ30+ days ago

Remote

Full-time

Produce and present external company presentations providing industry visibility for the organization; Continually suggesting solutions to solve issues in tune with organizational direction. Lead complex projects, programs and submissions, manages client meetings, CRMs, collaborates well with regulatory, PMs and sponsors.

Parsippany, New Jersey30+ days ago

$103,000–$140,000 Per Year

Write, test, and validate SAS programs to produce analysis datasets, TLGs and presentation output, to be included in reports for submission to regulatory agencies, publications and other communications as needed. The range considers a wide range of factors that are considered in making compensation decisions, including but not limited to: geographic markets, business or organizational needs, skill sets, experience, training, licensure, and certifications.

New York, NY30+ days ago

$90,000–$100,000

Additionally, candidates with experience working with electronic health record and administrative data (vital records, Medicaid/Medicare or other claims data) and with training or experience in reproductive epidemiology or application of statistical methods to clinical obstetrics and gynecology are highly desired. The Associate Research Scientist will work closely with Biostatistics faculty and clinical investigators in the Department of Obstetrics and Gynecology on application of statistical methods, data management, data workflows and monitoring across a wide range of areas.

New York City, NY30+ days ago

Remote

$260,000–$285,000 Per Year

Our industry-leading neuroscience portfolio includes FDA-approved treatments for major depressive disorder, excessive daytime sleepiness associated with narcolepsy and obstructive sleep apnea, and migraine, and multiple late-stage development programs addressing a broad range of serious neurological and psychiatric conditions that impact over 150 million people in the United States. Axsome Therapeutics is seeking a Senior Director, Health Economics and Outcomes Research (HEOR) Analytics to lead the design and execution of real-world evidence (RWE) analytics in support of the value proposition of Axsome's marketed products and pipeline assets.

Princeton, NJ30+ days ago

Full-time

For 25 years, its hard-working, innovative and collaborative team has invented next-generation antibody technology platforms and harnessed translational, quantitative and data sciences, resulting in a proprietary pipeline including bispecific T-cell engagers, antibody-drug conjugates, next-generation immune checkpoint modulators and effector function-enhanced antibodies. The Role : The Senior Director acts as a high-level statistical expert supporting the clinical development of compounds as therapeutic area lead, compound lead and/or indication lead for both early and late-stage programs and may also act as trial responsible statistician with responsibilities as described below.

New York, New York30+ days ago

$50–$60 Per Hour

This role is ideal for someone who can operate as a true partner to cross-functional teams, bringing both technical expertise and scientific insight to clinical data management activities. System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America.

Raritan, NJ30+ days ago

Remote

Full-time

Cambridge, Massachusetts, United States of America, Horsham, Pennsylvania, United States of America, New Brunswick, New Jersey, United States of America, Raritan, New Jersey, United States of America, San Diego, California, United States of America, Spring House, Pennsylvania, United States of America, Titusville, New Jersey, United States of America. OHDA's mission is to improve the lives of individuals and quality of healthcare by efficiently generating real-world evidence from the world's observational health data, transparently disseminating evidence-based insights to real-world decision-makers, and objectively advancing the science and technology behind reliable, reproducible real-world analytics.

New York, NY30+ days ago

$66,299.99–$85,000

In this role, the successful candidate supports health research by developing, managing, and documenting analytical datasets in collaboration with faculty, scientists, and statistical analysts within the Center for Surgical and Transplant Applied Research (CSTAR). This role will primarily focus on using SQL and related tools in a large-scale data environment to prepare research-ready datasets and support analytic workflows across a range of clinical and population health research projects.

New York, NY30+ days ago

$70,481.60–$105,000

This role is ideal for an someone with prior experience working in academic environments, strong programming and analytic skills, ability to independently lead and execute analyses to achieve study aims, and who enjoys collaborating with researchers and policy partners to translate data into actionable insights. The Senior Data Analyst will serve as the primary quantitative analyst on several projects and work closely with investigators to manage complex datasets, implement analytic plans, and produce reproducible analyses that support publications, grant proposals, and policy-relevant research outputs.

Trenton, NJ30+ days ago

The PV Analytics and Reporting Specialist, PV Analytics Center of Excellence contributes to the ongoing development, implementation, and successful execution of the scientific, operational, and regulatory reporting efforts in line with the overall WWPS needs. The PV Analytics and Reporting Specialist, PV Analytics Center of Excellence applies a combination of life sciences strategy, leadership, and reporting/visualization experience to drive successful servicing of information needs across WWPS.

New York, NY30+ days ago

$70,481.60–$105,000 Per Year

New York, NY30+ days ago

$66,299.99–$85,000 Per Year

New York, New York30+ days ago

$77,200–$96,500 Per Hour

Serves as the primary analytical owner for CMS Star Ratings Member Experience measures, including monitoring performance across CAHPS domains such as Getting Needed Care, Customer Service, Rating of Health Plan, and Care Coordination. Analyzes member engagement across operational touchpoints including care management interactions, call center contacts, grievances, and service utilization to identify drivers of member satisfaction and opportunities to improve member experience across the lifecycle of plan enrollment and engagement.

New York, New York30+ days ago

$109,900–$146,500 Per Year

Owns the end-to-end analytic approach for monitoring membership, medical expenses, utilization, and revenue trends; conducts advanced forensic investigations into anomalies and unfavorable trends; and develops executive-ready presentations, dashboards, and supporting documentation to inform strategic and operational decisions. Overview: Leads the compilation, analysis, and interpretation of healthcare clinical and utilization data to produce insights related to cost drivers and opportunities to improve affordability and clinical outcomes for current and prospective VNS Health members.

Parsippany, New Jersey30+ days ago

$141,000–$194,000 Per Year

The Associate Director is versed in statistical programming languages such as SAS, R, Python, etc. to perform programming in processing data at various levels, verifies analytical datasets, and applies conventional and novel statistical methods to summarize data and generate clinically meaningful results. Working closely with his/her manager, the Associate Director designs pain management studies of clinical/economic burden of diseases, unmet needs of patients, comparative effectiveness of treatments on economic/health outcomes across treatments.

New York, New York22 days ago

Remote

$50–$75 Per Hour

This role supports current and upcoming remote consulting opportunities focused on structured public health review, surveillance documentation, program evaluation materials, health policy analysis, grant and reporting workflows, outbreak documentation, and high-quality project execution. Familiarity with tools and systems such as Esri ArcGIS, Google Maps Platform, SAS, MATLAB, Socrata, Esri ArcGIS Hub, public-health dashboards, open-data portals, or similar analytical platforms.

Nutley, NJ30+ days ago

$200,091.38–$217,900 Per Year

Requirements: A Master's degree in Molecular and Cellular Biology, Biotechnology, or closely related plus 8 years of experience in Pharmaceutical industry experience in clinical development statistical programming methods and processes in job offered or related roles. Significant areas of oversight include SAS programming activities in support of Multiple Studies (Phase II -IIIB) for a single or multiple compounds within related therapeutic areas spanning inception through to submission.

New York, NY30+ days ago

$90,000–$100,000 Per Year

Piscataway, NJ13 days ago

$25–$30 Per Hour

Aligned with Rutgers University-New Brunswick and collaborating university wide, RBHS includes eight schools,a behavioral health network, and six centers and institutes that focus on cancer treatment and research, neuroscience, clinical and translational research, advanced biotechnology and medicine, environmental and occupational health, and health care policy and aging research. Under Policy 100.3.1 Immunization Policy for Covered Individuals, if employment will commence during Flu Season, Rutgers University may require certain prospective employees to provide proof that they are vaccinated against Seasonal Influenza for the current Flu Season, unless the University has granted the individual a medical or religious exemption.

Einstein/Resnick - Bronx, New York30+ days ago

POSITION RESPONSIBILITIES: Pipeline development and leadership: Design, implement, document, and maintain end-to-end NGS pipelines for microbiome and HPV genomics applications (e.g., 16S/ITS1 amplicon sequencing, shotgun metagenomics, viral/HPV sequencing, bisulfite sequencing, and viral integration analyses). The ideal candidate is an independent problem solver who is comfortable taking ownership of analysis workstreams, building and maintaining reproducible pipelines, and driving projects forward from raw data to interpretable outputs.

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Biostatistics Jobs in Linden, NJ

Director, Early Phase Biostatistics Daiichi Sankyo, Inc.

Director, Early Phase Biostatistics (m/f/d) Daiichi Sankyo, Inc.

Associate Director, Biostatistics (Late Stage) Daiichi Sankyo, Inc.

Head of Global Biostatistics Daiichi Sankyo, Inc.

Associate Director, Epidemiology Analytics Daiichi Sankyo, Inc.

Senior Director, Clinical Safety MD Daiichi Sankyo, Inc.

Manager, Statistical Programming (m/f)d) Daiichi Sankyo, Inc.

Pharmacovigilance (PV) Analytics and Reporting Specialist Eclaro

Senior Scientist, Biostatistics - Oncology Johnson and Johnson

Associate/Full Professor, Biostatistics-Tenure Track Albert Einstein College of Medicine

Associate Director Biostatistics Penfield Search Partners

Senior Director, Biostatistics Cellectis

Statistical Analyst and SAS Programmer R&G US Inc.

Senior Principal Biostatistician GLOBAL Recruitment Solutions LLC

Senior Biostatistician - Remote (US) MMS

Sr. Principal Statistics Globalchannelmanagement

Biostatistician Systimmune

Principal Biostatistician - Remote MMS

Manager, Statistical Programming Pacira Pharmaceuticals, Inc.

Associate Research Scientist NYU Langone Health

Senior Director, Health Economics and Outcomes Research (HEOR) Analytics Axsome Therapeutics

Senior Director, Statistician Genmab

Clinical Data Manager (STEM-Focused) System One

Manager, Observational Health Data Analytics Johnson and Johnson

Data Analyst, Center of Surgical and Transplant Applied Research (CSTAR) NYU Langone Health

Senior Data Analyst NYU Langone Health

C08 - MEDICAL AND REGULATORY AFFAIRS / PHARMACOVIG - PHARMACOVIGILANCE SPECIALIST TechDigital Corporation

Senior Data Analyst NYU Langone Medical Center

Data Analyst, Center of Surgical and Transplant Applied Research (CSTAR) NYU Langone Medical Center

Member Experience Data Analyst, Hybrid VNS Health

Lead Health Economics Analyst VNS Health

Associate Director, RWE Analytics Pacira Pharmaceuticals, Inc.

Remote 24-MAG

Associate Director, Statistical Programming Eisai

Associate Research Scientist NYU Langone Medical Center

Student Assistant (CANSAH-BC) Rutgers University

Bioinformatics Analyst Albert Einstein College of Medicine

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