Top 64 Sr Statistical Programmer Jobs

Sr. Statistical Programmer
Katalyst Healthcares & Life Sciences —Baltimore, MD
- Contract
- Computer science
- 6 years
- Computer Science
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Sr Statistical Programmer (NA Only)
Syneos - Clinical and Corporate - Prod —North Carolina
- $80,600 - $145,000 a year
- Full-time
- English
- Team management
- Travel
- Employee stock purchase plan
- Health insurance
Sr.Statistical Programmer
Katalyst Healthcares & Life Sciences —Boulder, CO
- Contract
- Computer science
- 6 years
- Computer Science
Quick Apply
Senior RWE/RWA Programmer - Remote
Penfield Search Partners —Fairfield, CT
- Contract
- Remote
- 7 years
- Analysis skills
- Senior level
Quick Apply
Statistical Programmer/Sr. Statistical Programmer
Arrowhead Pharmaceuticals —Los Angeles, CA
- $90,000 - $135,000 a year
- Master's degree
- Analysis skills
- Quality control
Sr Programmer-Sr Data Scientist/Analys Real-World Data (SAS/R)
Syneos - Clinical and Corporate - Prod —North Carolina
- $80,600 - $175,700 a year
- Full-time
- English
- Analysis skills
- Bachelor's degree
- Employee stock purchase plan
- Health insurance
SR. STATISTICAL PROGRAMMER
TruMinds Clinical —Frisco, TX
- $81,286 a year
- Full-time
- Management
- Computer Science
- Mid-level
SR. STATISTICAL PROGRAMMER ANALYST
TruMinds Clinical —Frisco, TX
- $81,286 a year
- Full-time
- Mid-level
- Office
- Master's degree
Senior Principal Statistical Programmer (Remote)
WCG —Cary, NC
- $104,750 - $128,000 a year
- Full-time
- Remote
- Master's degree
- 8 years
- Travel
- Continuing education credits
- Health insurance
9d
Sr Statistical Programmer (Oncology), Real World Evidence – FSP
IQVIA —Durham, NC
- $88,300 - $220,900 a year
- Full-time
- 3 years
- Master's degree
- SQL
3d
Senior Principal Statistical Programmer
Katalyst Healthcares & Life Sciences —Paramus, NJ
- Contract
- 6 years
- Doctor of Philosophy
- Organizational skills
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Senior Statistical Programmer
Katalyst Healthcares & Life Sciences —Lake Villa, IL
- Contract
- Computer science
- 6 years
- Computer Science
Quick Apply
Senior Statistical Programmer
Merck —Rahway, NJ
- $117,000 - $184,200 a year
- Full-time
- Computer science
- Computer Science
- Bachelor of Science
- Paid holidays
- Health insurance
9d
Senior Statistical Programmer
Immunocore —Gaithersburg, MD
- $93,000 - $155,000 a year
- Full-time
- Computer Science
- 5 years
- Office
Sr. Principal Biostatistician
Biogen —Remote
- $134,000 - $179,000 a year
- Full-time
- 3 years
- Analysis skills
- Continuous improvement
- Paid parental leave
- Employee stock purchase plan
Senior Systems Programmer, Healthcare Innovations
American Institutes for Research —Chicago, IL
- $135,000 - $165,000 a year
- Email
- Remote
- Master's degree
- 8 years
- Analysis skills
Sr Manager, Statistical Programming
Gilead Sciences —Foster City, CA
- $169,320 - $219,120 a year
- Full-time
- Hybrid work
- Computer science
- Computer Science
- Bachelor of Science
- Health insurance
- Dental insurance
3d
Sr. Scientist, Stat. Programming - Late-Stage (Non-Oncology) (Hybrid)
Merck —Rahway, NJ
- $117,000 - $184,200 a year
- Full-time
- Computer Science
- Bachelor of Science
- 3 years
- Paid holidays
- Health insurance
7d
Sr. Principal Analyst, Statistical Programming
Neurocrine Bioscience —San Diego, CA
- $156,900 - $214,000 a year
- Full-time
- Computer science
- Computer Science
- Computer literacy
- Paid holidays
- Health insurance
Senior Biostatistician
CPC Clinical Research —Aurora, CO
- $120,000 - $150,000 a year
- Full-time
- Remote
- Microsoft Excel
- 5 years
- Master's degree
- Paid holidays
- Disability insurance
Quick Apply

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Sr. Statistical Programmer

Katalyst Healthcares & Life Sciences -
Baltimore, MD

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Job Details

Contract

Qualifications

FDA submissions
SAS
SAS language
SQL
Bachelor's degree
Industry trends
CDISC standards
Regulatory submission editing and review
Communication with regulatory authorities for clinical trials
Cross-functional collaboration
Cross-functional communication
Data analysis software

Full Job Description

Job Description:

We are seeking a highly motivated and qualified individual to join our Clinical Department as a Senior Statistical Programmer and work as part of a team to drive success.
Ideal candidates will be self-motivated, independent, committed to the generation of high-quality data within a fast-paced and innovative research team.
The Senior Statistical Programmer will serve as the lead statistical programmer and is responsible for statistical programming activities such as designing, developing, validating, updating, and documenting SAS programs to generate analysis datasets, data listings, summary tables, and statistical graphs supporting statistical analyses.
This position requires close collaboration with cross-functional teams to ensure the integrity and accuracy of clinical data used in regulatory filings and internal reporting.

Responsibilities:

Independently develop, validate, document and troubleshoot SAS programs for the preparation of periodic internal reports, regulatory submissions, and ad hoc analyses.
Create and maintain analysis and submission datasets (ADaM, SDTM) in compliance with CDISC standards and regulatory guidance.
Design, develop, validate, update, and document SAS programs to generate analysis datasets, data listings, tables, and graphs of high quality in a timely manner.
Support submission activities including preparation of data packages, eCTD deliverables, and responses to regulatory agencies,
Communicate with team members about statistical programming related to trial timelines, data quality, and results interpretation.
Develop software tools, SAS macros and utilities to automate programming activities and improve programming efficiency and quality.
Create SAS macros or other tools to enhance the efficient delivery of statistical services, providing associated documentation and staff training as needed.
Program quality checks for clinical study raw data and report findings.
Review or author SDTM and ADaM specifications and datasets.
Manage CROs, including reviewing or validating statistical deliverables of vendors.
Provides input in the design and development of case report forms.
Contribute to the preparation of research reports and presentations for internal project teams, leadership team, and external audience.
Establish and maintain excellent working relationships with critical collaborative partners throughout the company.

Requirements:

Bachelor's degree in Biostatistics, Mathematics, Statistics, Computer Science, or related field
Minimum 6 years' experience in bio-pharma statistical programming
Advanced SAS programming skills in SAS/Base, SAS/Macro, SAS/STAT, SAS/Graph, and SAS/SQL with a demonstrated mastery of SAS/STAT procedures
Strong expertise in CDISC including SDTM, ADaM, and CDASH
Extensive experience in SAS macro functions and dynamic code generations.
Experience in regulatory submissions (e.g., NDAs and DSURs)
High attention to detail, with a focus on quality and traceability in all deliverables
Strong interpersonal and teamwork skills with a collaborative mindset and the ability to manage multiple priorities in a fast-paced and dynamic environment with shifting timelines and evolving needs
Take initiatives to solve problems proactively and think critically
Willing to adapt to changing business needs, able to pivot between tasks
Able to make complex programming and data-related decisions independently
Comprehensive knowledge and deep understanding of statistical programming environments, processes, procedures, and roles for clinical development from Phase 1 through regulatory submission
Up to date with CDISC standards, industry trends, best practices, and statistical programming methodology

Quick Apply

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