Top 43 Sas programmer Jobs in Edison, Nj

Director, Early Phase Biostatistics
Daiichi Sankyo, Inc. —Basking Ridge, NJ
- $201,840 - $302,760 a year
- 7 years
- Doctor of Philosophy
- Travel
FSP Principal Statistical Programmer (Remote)
Everest Clinical Research —Bridgewater, NJ
- $112,000 - $175,000 a year
- Remote
- Computer Science
- Doctor of Philosophy
- Mentoring
- AD&D insurance
- Disability insurance
Quick Apply
Principal Statistical Programmer (Remote)
Everest Clinical Research —Bridgewater, NJ
- $112,000 - $175,000 a year
- Remote
- Computer Science
- Doctor of Philosophy
- Mentoring
- AD&D insurance
- Disability insurance
Quick Apply
2d
Senior Programming Manager
Genmab —Plainsboro, NJ
- $128,080 - $192,120 a year
- Online Application
- Computer Science
- Master's degree
- 8 years
- Commuter assistance
- Paid parental leave
Director, Late Development Statistical Programming
Genmab —Princeton, NJ
- $186,880 - $280,320 a year
- Online Application
- Computer science
- Computer Science
- 11+ years
- Commuter assistance
- Paid parental leave
Statistical Analyst and SAS Programmer
R&G US Inc. —Somerset, NJ
- $72,000 a year
- Email
- Writing skills
- English
- Mid-level
Quick Apply
SAS Programmer
Oasis Technology Inc. —East Brunswick, NJ
- Email
- Computer science
- Computer Science
- Bachelor of Science
Quick Apply
Junior Statistical Programmer
Oasis Technology Inc. —East Brunswick, NJ
- Contract
- Computer science
- Computer Science
- Bachelor of Science
Quick Apply
Senior Statistician
Katalyst Healthcares & Life Sciences —Edison, NJ
- Contract
- 6 years
- Doctor of Philosophy
- Organizational skills
Quick Apply
Clinical SAS Programmer
RR Solutions —Parsippany-Troy Hills, NJ
- Senior level
Sr. Statistical Programmer
Katalyst Healthcares & Life Sciences —Bridgewater, NJ
- Contract
- 6 years
- Management
- Computer Science
Quick Apply
Sr. Manager, Biostatistician / Programmer
Legend Biotech US —Somerset, NJ
- Full-time
- Master's degree
- Analysis skills
- Continuous improvement
Quick Apply
Associate Principal Scientist, Stat. Programming - A&R Standards, Innovation (Hybrid)
Merck —Rahway, NJ
- $142,400 - $224,100 a year
- Full-time
- Computer science
- 7 years
- Computer Science
- Paid holidays
- Health insurance
Manager Statistical Programming
Regeneron —Warren, NJ
- $128,600 - $210,000 a year
- Computer science
- Computer Science
- 8 years
- Disability insurance
- Health insurance
Principal Statistical Programmer
Regeneron —Warren, NJ
- $109,900 - $179,300 a year
- 3 years
- Master's degree
- Quality control
- Disability insurance
- Health insurance
Director, Real World Data & Epidemiology (RWD & EPI) Analytics
Genmab —Princeton, NJ
- $231,280 - $346,920 a year
- Online Application
- Master's degree
- Doctor of Philosophy
- Quality control
- Commuter assistance
- Paid parental leave
Clinical SAS Programmer
Katalyst Healthcares & Life Sciences —Newark, NJ
- Multiple hires
- Computer Science
- Bachelor of Science
- Writing skills
Quick Apply
Sr Clinical Shiny Developer
Katalyst Healthcares & Life Sciences —Avenel, NJ
- Contract
- Mentoring
- Linux
- Senior level
Quick Apply
Senior Manager, Statistical Programming
Regeneron —Warren, NJ
- $150,500 - $245,500 a year
- Computer Science
- Bachelor of Science
- Bachelor's degree
- Disability insurance
- Health insurance
Director, Clinical Data Management
PTC Therapeutics, Inc. —South Plainfield, NJ
- $200,700 - $252,600 a year
- Full-time
- Hybrid work
- Java
- C++
- Supervising experience
- Dental insurance
- Vision insurance
Quick Apply
3d

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sas programmer jobs near edison, nj

Director, Early Phase Biostatistics

Daiichi Sankyo, Inc. -
Basking Ridge, NJ

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Job Details

$201,840 - $302,760 a year

Qualifications

Statistics
Statistics
Biostatistics-based research
Statistics research
Doctor of Philosophy
Pharmaceutical company experience
Data analysis software

Full Job Description

Job Title:
Director, Early Phase Biostatistics

Job Requisition ID:
1342

Posting Start Date:
4/10/26

At Daiichi Sankyo, we are united by a single purpose, to improve lives around the world through innovative medicines. With a legacy of innovation since 1899, a presence in more than 30 countries, and more than 19,000 employees, we are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases, and immune disorders. Guided by our 2030 vision to "be an innovative global healthcare company contributing to the sustainable development of society", we are shaping a healthier, more hopeful future for patients, their families, and society.

Job Summary

Position leads multiple early phase compounds or complex studies contributing to clinical development plan, and responsible for statistical design, analysis and interpretation of results independently with minimal supervision. This position provides strategic inputs to entire drug development plans with minimal supervision and regulatory responses and other documents with minimal supervision. This position interacts with global project teams and global Health Authorities, as well as contract research organization (CRO) programmers and statisticians. Additionally, this position works under minimal supervision to solve complex project problems. This position utilizes innovative trial designs and modeling to optimize the statistical handling in the projects, in collaboration with statistical innovation group, precision medicine biostat group, and real-world data (RWD) group. This position collaborates with cross functional project leaders from translational medicine, clinical operation, CSPV, clinical development and other functions in GPTs

Responsibilities

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. Leads the implementation of statistical methodologies and addresses specific statistical issues in the design and modeling of responsible clinical studies.

Act as statistical expert in the assigned projects. Guides the project team in using the most efficient or innovative study design by considering the regulatory agencies’ requirements for the country and Regions the compound will be submitted, and helps to maximize the success of the drug product. May also serve as a lead statistician for certain studies and ensures the study designs are scientifically sound, the efficacy and safety information meets regulatory requirements of the countries and Regions the drugs will be submitted. Ensures consistency in -derived data definition, - statistical analysis and result interpretation; Leads the planning and analysis of integrated efficacy and safety data.

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).

CRO / Vendor Interaction: Participates in reviewing the proposal for CRO selection. Reviews and negotiates - timelines; Guides CRO biostatistician and statistical programmers on assigned projects to ensure consistency in derived data definition, - analysis methodologies, and interpretation of analysis results. Ensures timely delivery of high quality deliverables.

Global Health Authority Interaction / Negotiation: Authors documents and responses submitted to Health Authorities globally with some guidance from supervisor. Represents statistics function to Health Authorities meetings as needed.

Initiatives and harmonization to improve drug development: Lead or contribute to initiatives to optimize the process and save cost in drug development.

Qualifications

Education

PhD in statistics or biostatistics required

Work Experience

7+ years of relevant experience in the pharmaceutical industry required

Competencies

Expert knowledge of drug development and statistical methodologies.

Excellent programming skills in SAS and/or R.

Excellent oral and written communication skills.

Working knowledge of statistical software package such as NQUERY, EAST, etc.

Excellent Project planning skills.

Demonstrated expertise in trial design and data analysis.

Excellent collaborating skills.

Travel Requirements

Ability to travel up to 20%

International travel may be required

Daiichi Sankyo, Inc. is an equal opportunity/affirmative action employer. Qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, age, or any other characteristic protected by law.

Salary Range:
USD$201,840.00 - USD$302,760.00

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Refine Your Search

sas programmer jobs in edison, nj

Director, Early Phase Biostatistics

FSP Principal Statistical Programmer (Remote)

Principal Statistical Programmer (Remote)

Senior Programming Manager

Director, Late Development Statistical Programming

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Sr. Statistical Programmer

Sr. Manager, Biostatistician / Programmer

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Manager Statistical Programming

Principal Statistical Programmer

Director, Real World Data & Epidemiology (RWD & EPI) Analytics

Clinical SAS Programmer

Sr Clinical Shiny Developer

Senior Manager, Statistical Programming

Director, Clinical Data Management

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