11 Results for

Statistician Jobs in New Jersey

Jobs

Basking Ridge, NJ9 days ago

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, NJ9 days ago

$201,840–$302,760 Per Year
Full-time

Basking Ridge, NJ9 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.

New Brunswick, NJ30+ days ago

Extensive knowledge on statistical methodologies, such as design of experiment (DOE), linear and nonlinear regression, mixed model, statistical process control (SPC), and multivariate analysis. The successful candidate will provide statistical support to Global Product Development & Supply (GPS) and late stage development to deliver process and method robustness in ensuring product quality and compliance.

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.

Somerset, New Jersey15 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.

Jersey City, NJ14 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.

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.

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 Jersey13 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.

Resume Resources

Free Resume Templates Free Resume Builder

Get noticed by top employers!

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

Create A Free Account

Statistician Jobs in New Jersey

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

Director, Early Phase Biostatistics Daiichi Sankyo, Inc.

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

Quality - statistician TechDigital Corporation

Senior Director, Statistician Genmab

Statistical Analyst and SAS Programmer R&G US Inc.

Senior Biostatistician - Remote (US) MMS

Principal Biostatistician - Remote MMS

Senior Principal Biostatistician GLOBAL Recruitment Solutions LLC

Sr. Principal Statistics Globalchannelmanagement

Resume Resources