Top 255 Sas Programmer Clinical Jobs

Associate Director, Statistical Programming
EPM Scientific —Philadelphia, PA
- $160,000 - $200,000 a year
- Master's degree
- 8 years
- Bachelor's degree
Quick Apply
6d
Director, Statistical Programming
CSL Behring —King of Prussia, PA
- $239,000 - $308,000 a year
- Full-time
- Computer science
- Computer Science
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Associate Director Oncology Biostatistics
Penfield Search Partners —San Francisco, CA
- 5 years
- Doctor of Philosophy
- Quality control
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Principal Statistical Programmer (Remote)
Everest Clinical Research —Bridgewater, NJ
- $112,000 - $175,000 a year
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- Doctor of Philosophy
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FSP Principal Statistical Programmer (Remote)
Everest Clinical Research —Bridgewater, NJ
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- Remote
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Senior Statistical Programmer
MM Infotech —Remote
- Full-time
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VENESCO, LLC —Falls Church, VA
- Full-time
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- 5 years
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Clinical SAS Programmer
NoyMed CRO —Remote
- Full-time
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Clinical Data Programmer I
Perceptive —Remote
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- Full-time
- Remote
- Computer science
- Computer Science
- SQL
- Health savings account
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SAS Statistical Programmer
Cardiovascular Research Foundation —New York, NY
- $85,000 - $95,000 a year
- Full-time
- Hybrid work
- Computer Science
- Mid-level
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SAS Programmer
Oasis Technology Inc. —East Brunswick, NJ
- Email
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- Bachelor of Science
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Clinical SAS Programmer
RR Solutions —Parsippany-Troy Hills, NJ
- Senior level
SAS Programmer
BioInforMedica —West Chester, PA
- Computer Science
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Katalyst Healthcares & Life Sciences —Newark, NJ
- Multiple hires
- Computer Science
- Bachelor of Science
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SAS Programmer
Katalyst Healthcares & Life Sciences —San Francisco, CA
- Contract
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- 7 years
- Master's degree
- Bachelor's degree
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Junior Statistical Programmer
Oasis Technology Inc. —East Brunswick, NJ
- Contract
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- Computer Science
- Bachelor of Science
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Principal SAS Programmer
Princeton Pharmatech —New Jersey
- 5 years
- Analysis skills
- Doctor of Philosophy
SAS Programmer
CICONIX, LLC —Fort Detrick, MD
- Full-time
- Background check
- Mid-level
- Office
- Paid time off
Quick Apply
Sr. Statistical Programmer
Kodiak Sciences Inc. —Palo Alto, CA
- Full-time
- Computer Science
- 5 years
- Bachelor of Science
11d
Senior Clinical Programmer Contractor
Arcus Biosciences —Remote
- Contract
- Remote
- Computer Science
- Mid-level
- Master's degree
13d

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Associate Director, Statistical Programming

EPM Scientific -
Philadelphia, PA

Quick Apply

Job Details

$160,000 - $200,000 a year
6 days ago

Qualifications

SAS
SAS language
ICH guidelines
Bachelor's degree
Pharmaceutical company experience
CDISC standards
Vendor communication
Cross-functional collaboration
Data analysis software

Full Job Description

Title: Principal / Associate Director, Statistical Programming

Location: King of Prussia, PA (Hybrid)

I am currently partnered with a leading pharmaceutical organization seeking an Individual Contributor, Statistical Programmer to lead programming activities across multiple clinical development programs spanning the full drug development lifecycle.

Key Responsibilities

Lead and support statistical programming activities across multiple clinical studies and development programs.
Develop, validate, review, and maintain SAS programs for data manipulation, analysis, reporting, and submission.
Review external vendor deliverables (e.g., SDTM, ADaM, TLFs, Define.xml packages) to ensure accuracy, quality, and compliance with standards.
Contribute to regulatory submissions, including NDA/BLA filings, integrated summaries (ISS/ISE), pooled analyses, and responses to health authorities.

Qualifications

Bachelor's degree in Statistics, Mathematics, etc. (Masters Preferred)
8+ years of statistical programming experience within the pharmaceutical or biotechnology industry.
Strong proficiency in SAS programming
Deep understanding of regulatory guidelines (ICH, GCP) and industry standards.
Extensive experience with CDISC standards, including SDTM and ADaM
Prior involvement in regulatory submissions (NDA/BLA) and associated deliverables (e.g., Define.xml, validation processes) preferred.
Strong communication, organizational, and cross-functional collaboration skills.
Solid knowledge of statistical methodologies applied to clinical trial data.
Demonstrated experience working with or overseeing external CRO partners.

Quick Apply

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