Top 11 Sas programmer Jobs in Philadelphia Pa

Associate Director Biostatistics
Penfield Search Partners —Pennsylvania
- 7 years
- English
- Office
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Statistical Analytical Programmer
Slipstream IT —Blue Bell, PA
- Full-time
- Remote
- 5 years
- Bachelor of Science
- Travel
- Disability insurance
- Health insurance
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SDTM, Clinical SAS Programmer
Katalyst Healthcares & Life Sciences —North Wales, PA
- Contract
- Senior level
- 10 years
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SR. CLINICAL SAS PROGRAMMER
ACL Digital —King of Prussia, PA
- Email
- Computer science
- Computer Science
- Quality control
SAS Programmer
BioInforMedica —West Chester, PA
- Computer Science
- Bachelor of Science
- Bachelor's degree
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
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
TO APPLY PLEASE SEND US AN EMAIL >
Inference —Chesterbrook, PA
- 5 years
- Mentoring
- Senior level
Sr. Manager/ Associate Director, Statistical Programming
Avalo Therapeutics —Chesterbrook, PA
- 7 years
- Computer Science
- Master's degree
Quick Apply
Principal Statistical Programmer (Remote)
Everest Clinical Research —United States
- $112,000 - $175,000 a year
- Remote
- Computer Science
- Doctor of Philosophy
- Mentoring
- AD&D insurance
- Disability insurance
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Associate Director Biostatistics

Penfield Search Partners
Pennsylvania

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Job Details

Qualifications

Pharmaceutical research experience

Full Job Description

Associate Director, Biostatistics
Location: Greater Philadelphia or Boston
Work Model: Hybrid (3 days onsite per week)

Our client is a global organization focused on advancing novel therapies for patients with rare diseases, with a clinical pipeline spanning multiple therapeutic areas and stages of development. Bringing a collaborative, project-driven structure, the organization is building a forward-looking team dedicated to delivering treatments that make a meaningful impact worldwide.

Currently they are seeking an Associate Director, Biostatistics to provide statistical leadership for clinical development programs. In this role, you will develop and implement statistical strategies for clinical trials and regulatory submissions, contributing to study design, data analysis, and reporting. This position offers strong visibility and requires close collaboration with cross-functional teams as well as interactions with regulatory agencies both in the U.S. and internationally. It’s a fantastic opportunity to become a part of a stable and growing group with a focus on innovation.

Responsibilities

Lead the full scope of Biostatistics activities for a clinical development program within a therapeutic area.
Define statistical strategy and ensure appropriate statistical methodologies are applied to study design and data analysis for clinical trials and regulatory submissions.
Influence and contribute to clinical development plans and collaborate with cross-functional teams for governance reviews.
Lead statistical strategy for study planning and execution as a member of the Study Executive Team and Clinical Development Team.
Provide quantitative evaluation supporting clinical trials, regulatory submissions, and related documentation.
Provide statistical thought partnership for innovative study design and clinical development plans, including Go/No-Go criteria and probability of technical success calculations.
Plan and oversee program-wide statistical analyses and ensure the quality and timely delivery of interim and final results, including integrated analyses for submissions.
Represent Biostatistics in interactions with regulatory authorities such as the FDA, EMA, and PMDA.
Interpret analysis results and ensure accuracy in study reports and regulatory documents.
Manage outsourcing operations or collaborate with internal statistical programmers within the program.
Ensure the quality and timeliness of deliverables from CROs or functional service providers.
Support or lead improvement initiatives within the department, organization, or broader pharmaceutical industry.
Prepare abstracts, posters, oral presentations, and written reports to communicate results of clinical programs and studies to internal and external stakeholders.

Qualifications

PhD or MS in Biostatistics, Statistics, or a related field
PhD with 7 years of experience or MS with 9 years of experience in drug development
Experience providing statistical leadership at the compound or indication level
Demonstrated expertise in facilitating and optimizing clinical development strategies across early, late, or full development phases
Experience supporting regulatory submissions
Experience interacting with major regulatory authorities preferred
Experience working with CROs or managing internal statistical deliverables preferred
Demonstrated track record of innovation preferred

Core Competencies

Familiarity with regulatory guidance and regulatory interactions
Broad knowledge of clinical development processes
Ability to work collaboratively and provide leadership in a matrix environment
Strong written and verbal communication skills in English
Good working knowledge of SAS and/or R
Expertise across a range of statistical methodologies
Experience applying innovative or creative statistical methods for clinical data analysis
Familiarity with CDISC standards, statistical programming, and data standards

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Refine Your Search

sas programmer jobs in philadelphia pa

Associate Director Biostatistics

Statistical Analytical Programmer

SDTM, Clinical SAS Programmer

SR. CLINICAL SAS PROGRAMMER

SAS Programmer

Bioinformation B

Senior Programmer, EDC Systems

TO APPLY PLEASE SEND US AN EMAIL >

Sr. Manager/ Associate Director, Statistical Programming

Principal Statistical Programmer (Remote)

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