22 Results for

Biostatistics Jobs in Bridgewater, NJ

Jobs

Basking Ridge, NJ12 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, NJ12 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, NJ10 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, NJ12 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, NJ12 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, NJ12 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, NJ12 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.

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.

Somerset, New Jersey18 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.

Paramus, New Jersey16 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, NJ12 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).

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.

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.

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.

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.

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.

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.

Resume Resources

Free Resume Templates Free Resume Builder

Get noticed by top employers!

Upload your resume to let employers know you're open to Biostatistics job opportunities. Plus, receive relevant job recommendations in your inbox.

Create A Free Account

Biostatistics Jobs in Bridgewater, 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 Director Biostatistics Penfield Search Partners

Statistical Analyst and SAS Programmer R&G US Inc.

Senior Principal Biostatistician GLOBAL Recruitment Solutions LLC

Sr. Principal Statistics Globalchannelmanagement

Biostatistician Systimmune

Manager, Statistical Programming Pacira Pharmaceuticals, Inc.

Senior Director, Statistician Genmab

Associate Director, RWE Analytics Pacira Pharmaceuticals, Inc.

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

Manager, Observational Health Data Analytics Johnson and Johnson

Associate Director, Statistical Programming Eisai

Resume Resources