Top 12 Sas programmer Jobs in Lansdale Pa

Senior Programmer, EDC Systems
CSL Behring —King of Prussia, PA
- $143,000 - $169,000 a year
- Full-time
- Hybrid work
- Computer science
- Computer Science
- 5 years
Statistical Analytical Programmer
Slipstream IT —Blue Bell, PA
- Full-time
- Remote
- 5 years
- Bachelor of Science
- Travel
- Disability insurance
- Health insurance
Quick Apply
Statistical Analyst/Programmer
Temple University —Philadelphia, PA
- $75,000 - $85,000 a year
- Full-time
- Hybrid work
- Microsoft Access
- Mid-level
- Microsoft Office
- Paid holidays
- Health insurance
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Inference —Chesterbrook, PA
- 5 years
- Mentoring
- Senior level
Bioinformation B
University of Pennsylvania —Philadelphia, PA
- $67,155 - $101,500 a year
- Full-time
- Background check
- Computer Science
- Mid-level
- Health insurance
- Dental insurance
SDTM, Clinical SAS Programmer
Katalyst Healthcares & Life Sciences —North Wales, PA
- Contract
- Senior level
- 10 years
Quick Apply
13d
Associate Director, Biostatistics
CSL —King of Prussia, PA
- $212,000 - $251,000 a year
- Multiple hires
- Hybrid work
- English
- 8 years
- Doctor of Philosophy
Associate Director Biostatistics
Penfield Search Partners —Pennsylvania
- 7 years
- English
- Office
Quick Apply
Senior Scientist, Statistical Programming
Merck —North Wales, PA
- $117,000 - $184,200 a year
- Full-time
- Computer Science
- 3 years
- Travel
- Paid holidays
- Health insurance
Sr. Manager/ Associate Director, Statistical Programming
Avalo Therapeutics —Chesterbrook, PA
- 7 years
- Computer Science
- Master's degree
Quick Apply
Associate Director, Biostatistics
CSL Behring —King of Prussia, PA
- $212,000 - $251,000 a year
- Multiple hires
- Hybrid work
- English
- 8 years
- Doctor of Philosophy
4d

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Senior Programmer, EDC Systems

CSL Behring -
King of Prussia, PA

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Job Details

Full-time
$143,000 - $169,000 a year

Qualifications

Data integrity assurance
Data Integration (Data management)
Clinical research
Data validation techniques
XML
Writing skills
System design
English
System design for system development
Bachelor's degree
Pharmaceutical company experience
CDISC standards
Schema mapping design
Clinical quality assurance standards
Relational database design
Cross-functional communication
Validation design

Full Job Description

Position Purpose:

The Senior EDC Programmer focuses on governance, review, and validation of deliverables to ensure alignment with CSL standards, regulatory requirements, and industry best practices. The incumbent applies strong expertise in leading and overseeing set-up and maintenance of Clinical Data Management Systems in addition to providing technical support. This individual supports cross-functional teams such as Statistics, Data Management and Standards by overseeing and ensuring the quality of clinical data build and programming activities across in-house, hybrid, and vendor-supported studies. The role will contribute to shaping future-state data capabilities by supporting initiatives around scalable

data platforms and AI-driven automation, enabling more efficient and intelligent use of clinical data.

Reporting Relationships:

This role reports to the Director, Statistical Programming Lead

Work Environment:

*** On site / Hybrid at CSL Behring requires a minimum of 3 days in the designated work location office weekly for this role. Relocation and mobility assistance is not provided.

Main Responsibilities and Accountabilities:

Drive activities related to the design, development, and maintenance of clinical study databases by applying advanced technical expertise in: CRF design; database build; edit check programming; report development; custom programming; system interface configuration; and the implementation of all relevant systems features to support high-quality, compliant clinical data management.
Collaborate with clinical study teams, Standards (CDASH/SDTM,CSL), and cross-functional stakeholders to define, implement, and continuously enhance data quality methods, acceptance criteria, and validation rules for eCRF and external data sources across all study models
Oversee the implementation and maintenance of data quality control frameworks, including validation check libraries and acceptance criteria for vendor and internally generated data, ensuring alignment with CSL standards and regulatory expectations
Govern and maintain a standardized library of reports and listings to support study teams, ensuring consistency, reusability, and efficiency across in-house, hybrid, and vendor-supported studies
Oversee the setup, automation, and monitoring of recurring data quality and operational reports across different models (in-house vs outsourced etc.)a ensuring accuracy, completeness, and timely availability of outputs
Partner with Data Management, Statistics, and vendors to review and validate clinical data deliverables, ensuring submission readiness in accordance with regulatory standards (e.g., SDTM, define.xml)
Lead the reporting solutions that provide insights into data quality, study progress, and key metrics to support informed decision-making
Ensure appropriate data structures, storage, and integration approaches that enable pooled analyses, traceability, and efficient retrieval of both current and legacy clinical data
Support the integration and governance of external data sources (e.g., IxRS, eDiaries, labs, ECG), ensuring data consistency, quality, and alignment with study requirements, while facilitating collaboration between internal teams and vendors
Contribute to innovation and future-state initiatives by supporting the development of scalable data platforms, automation strategies, and AI-enabled capabilities to enhance data processing, validation, and analytics

Job Qualifications and Experience Requirements:

Education

BSc in Computer Science, Mathematics, Statistics or related area with relevant experience
Medidata Rave Study Builder Certification is preferred

Experience

5+ years of relevant experience with clinical database design in EDC systems within a pharmaceutical or CRO environment
Exposure to in-house, hybrid, and/or vendor-supported study models
Familiarity/practical experience with CDISC standards, particularly CDASH, SDTM including data mapping, validation, and activities supporting submission readiness
Proficiency with EDC systems (e.g., Medidata Rave, Veeva Vault) and understanding of eCRF design and clinical data collection frameworks
Strong understanding of clinical data processes, including data standards, data flows, and integration of eCRF and external data sources, data quality oversight, validation processes, and vendor deliverable review
Proven ability to manage priorities, meet timelines, and operate effectively in a fast-paced and evolving environment
Ability to independently perform data migration activities for post-production study changes is preferred
Experience with C# is preferred and familiarity with SAS, Python, or R is a plus

Competencies

Good communication and analytical skills
Good planning and organizational skills
Ability to work successfully in a matrix organizational structure
Networking skills and ability to share knowledge and experience amongst colleagues
Fluent in English, oral and in writing

The expected base salary range for this position at hiring is $143,000 - $169,000. Please note this salary range reflects the minimum and maximum base pay that CSL expects to pay for this position at the listed for the Waltham, MA USA work location at the time of this posting. Individual base salary for a successful candidate is determined by qualifications, skill level, experience, competencies and other relevant factors. In addition to base salary, total compensation for this role may also include incentive compensation and equity.

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sas programmer jobs in lansdale pa

Senior Programmer, EDC Systems

Statistical Analytical Programmer

Statistical Analyst/Programmer

TO APPLY PLEASE SEND US AN EMAIL >

Bioinformation B

SDTM, Clinical SAS Programmer

Associate Director, Biostatistics

Associate Director Biostatistics

Senior Scientist, Statistical Programming

Sr. Manager/ Associate Director, Statistical Programming

Associate Director, Biostatistics

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