Top 237 Clinical sas programmers Jobs

Director, Early Phase Biostatistics
Daiichi Sankyo, Inc. —Basking Ridge, NJ
- $201,840 - $302,760 a year
- 7 years
- Doctor of Philosophy
- Travel
SQL Programmer
VA Boston Healthcare System —Boston, MA
- Full-time
- Background check
- SQL
- Bachelor's degree
- Health savings account
- Health insurance
Quick Apply
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
Manager, Clinical Programming (Remote)
Penfield Search Partners —Fairfield, CT
- Contract
- Remote
- Computer Science
- Bachelor's degree
- Organizational skills
Quick Apply
4d
Associate Director Biostatistics
Penfield Search Partners —Pennsylvania
- 7 years
- English
- Office
Quick Apply
Associate Director Oncology Biostatistics
Penfield Search Partners —San Francisco, CA
- 5 years
- Doctor of Philosophy
- Quality control
Quick Apply
Principal Statistical Programmer - Global Studies- REMOTE
Penfield Search Partners —Fairfield, CT
- Contract
- Remote
- Computer Science
- 5 years
- Master's degree
Quick Apply
Clinical SAS Programmer
Katalyst Healthcares & Life Sciences —Newark, NJ
- Multiple hires
- Computer Science
- Bachelor of Science
- Writing skills
Quick Apply
Clinical SAS Programmer
RR Solutions —Parsippany-Troy Hills, NJ
- Senior level
SAS Programmer
VENESCO, LLC —Falls Church, VA
- Full-time
- Remote
- 5 years
- Master's degree
- Bachelor's degree
Quick Apply
Senior / Principal Statistical Programmer, Clinical Development Data Services, R&D, Orion Corporation
Orion Corporation —Boston, MA
- $100,000 - $180,000 a year
- Full-time
- Computer Science
- 5 years
- Office
10d
Clinical Data Programmer I
Perceptive —Remote
- $52,520 - $75,000 a year
- Full-time
- Remote
- Computer science
- Computer Science
- SQL
- Health savings account
- Paid holidays
Programmer Analyst (SAS or R) (Job 1366)
DLH —Atlanta, GA
- $50,000 - $80,000 a year
- Mid-level
- Master's degree
- SQL
- AD&D insurance
- Disability insurance
Quick Apply
Clinical Data Manager
SystImmune —Redmond, WA
- $100,000 - $170,000 a year
- Full-time
- Bachelor of Science
- Mid-level
- Office
- Paid holidays
- Disability insurance
Sr. Clinical Programmer
Syneos - Clinical and Corporate - Prod —Delaware
- $80,600 - $145,000 a year
- Full-time
- Microsoft Excel
- Bachelor's degree
- Travel
- Employee stock purchase plan
- Health insurance
Manager, Clinical Data Management
Immunocore —Radnor, PA
- $107,250 - $178,750 a year
- Full-time
- 5 years
- Bachelor of Science
- Writing skills
Statistical Programming Lead, Clinical Development Data Services, R&D, Orion Corporation
Orion Corporation —Boston, MA
- $130,000 - $230,000 a year
- Full-time
- Computer Science
- Office
- Master's degree
10d
SAS Programmer
BioInforMedica —West Chester, PA
- Computer Science
- Bachelor of Science
- Bachelor's degree
Clinical Data Analyst
SimulStat —Remote
- Contract
- 7 years
- Master's degree
- Bachelor's degree

I want to receive the latest job alert for clinical sas programmers

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

Director, Early Phase Biostatistics

Daiichi Sankyo, Inc. -
Basking Ridge, NJ

Apply Now

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

Download Our Benefits Summary PDF

Professionals

Apply Now

Refine Your Search

clinical sas programmers jobs

Director, Early Phase Biostatistics

SQL Programmer

FSP Principal Statistical Programmer (Remote)

Principal Statistical Programmer (Remote)

Manager, Clinical Programming (Remote)

Associate Director Biostatistics

Associate Director Oncology Biostatistics

Principal Statistical Programmer - Global Studies- REMOTE

Clinical SAS Programmer

Clinical SAS Programmer

SAS Programmer

Senior / Principal Statistical Programmer, Clinical Development Data Services, R&D, Orion Corporation

Clinical Data Programmer I

Programmer Analyst (SAS or R) (Job 1366)

Clinical Data Manager

Sr. Clinical Programmer

Manager, Clinical Data Management

Statistical Programming Lead, Clinical Development Data Services, R&D, Orion Corporation

SAS Programmer

Clinical Data Analyst

I want to receive the latest job alert for clinical sas programmers

Related Searches

Explore jobs in more locations

Job Seeker Tools

Employer Tools

Browse

Stay Connected