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Senior Principal Sas Programmer Jobs in Delaware

Cytel

Principal Biostatistician FSP

Dover, DE

An experienced Principal Biostatistician with a passion for clinical development and analysis ... SAS programming skills for QCing critical outputs, Efficacy/Safety tables, and working closely with ...

New

Cytel

Principal Biostatistician FSP

Dover, DE

An experienced Principal Biostatistician with a passion for clinical development and analysis ... SAS programming skills for QCing critical outputs, Efficacy/Safety tables, and working closely with ...

New

Ra

Marketing Analytics Senior Manager

Wilmington, DE · On-site

Who is proficient in SAS or other statistical modeling tools. Who enjoys traveling, because this ... Who is proficient in Applied Statistics/Econometrics, Statistical Programming, Database Marketing ...

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Senior Principal Sas Programmer information

What is a senior principal SAS programmer?

Senior Principal SAS Programmers are highly experienced professionals who specialize in using SAS (Statistical Analysis System) software to analyze and manage large datasets, especially in industries such as pharmaceuticals, healthcare, and finance. They lead statistical programming activities, develop complex programs for data analysis, and ensure the quality and integrity of deliverables. In addition to their technical expertise, they often mentor junior programmers, provide guidance on best practices, and collaborate closely with statisticians and project teams to support regulatory submissions and clinical trials.

How does a senior principal SAS programmer typically collaborate with cross-functional teams in clinical research projects?

A Senior Principal SAS Programmer frequently works alongside biostatisticians, data managers, and clinical research associates to ensure the accuracy and integrity of clinical trial data. They are often responsible for developing and validating complex programs for data analysis and reporting, as well as providing technical guidance to junior programmers. Effective communication and a collaborative mindset are crucial, as they must interpret statistical analysis plans and translate them into SAS code while aligning with regulatory requirements and project timelines. This cross-functional teamwork is essential for meeting project milestones and delivering high-quality submissions.

What are the key skills and qualifications needed to thrive as a senior principal SAS programmer, and why are they important?

To thrive as a Senior Principal SAS Programmer, you need advanced expertise in SAS programming, statistical analysis, and a strong background in life sciences or a related field, often supported by a relevant degree. Mastery of SAS Base, SAS Macro, and SDTM/ADaM standards, as well as experience with clinical trial data management systems and regulatory submission processes, is crucial. Exceptional problem-solving, attention to detail, and effective communication skills help you lead projects and collaborate with cross-functional teams. These skills ensure the accuracy, efficiency, and compliance of clinical data analysis, which is vital for regulatory approvals and successful study outcomes.

What is the difference between Senior Principal Sas Programmer vs SAS Data Scientist?

AspectSenior Principal Sas ProgrammerSAS Data Scientist
Required CredentialsBachelor's/Master's in Computer Science, Statistics, or related field; SAS certificationsBachelor's/Master's in Data Science, Statistics, or related; SAS certifications often preferred
Work EnvironmentPharmaceutical, healthcare, or biotech industries; focus on programming and data managementResearch, analytics, and modeling in various industries; focus on data analysis and predictive modeling
Employer & Industry UsageUsed in clinical trials, regulatory submissions, and data managementUsed in analytics, machine learning, and business intelligence projects

The Senior Principal Sas Programmer primarily focuses on advanced SAS programming for clinical and regulatory data, while the SAS Data Scientist emphasizes data analysis, modeling, and insights. Both roles require SAS expertise and often overlap in data handling, but their core responsibilities and industry applications differ.

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For Senior Principal Sas Programmer jobs in Delaware, the most frequently searched job titles are:

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The top searched job categories for Senior Principal Sas Programmer jobs in Delaware are:

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Cities in Delaware with the most Senior Principal Sas Programmer job openings:

Senior Principal Sas Programmer jobs near you
Infographic showing various Senior Principal Sas Programmer job openings in Delaware as of August 2026, with employment types broken down into 87% Full Time, 11% Part Time, 1% Temporary, and 1% Contract. Highlights an 91% Physical, 2% Hybrid, and 7% Remote job distribution.

Principal Biostatistician FSP

Cytel

Dover, DE

Full-time

Posted yesterday

New

Job description

Who Are You?

An experienced Principal Biostatistician with a passion for clinical development and analysis, adept at utilizing advanced statistical methods, you will lead one Phase I-IV clinical studies across your region. You are excited and enthusiastic, motivate your teams to do great work and collaborate easily with your clients. You never settle for what is, but always push clinical development forward to what it could be. You motivate others to do the same.

Sponsor-dedicated:

Working fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you, you'll be at the heart of our client's innovation. As a Biostatistician you will be dedicated to one of our global pharmaceutical clients; a company that is driving the next generation of patient treatment, where individuals are empowered to work with autonomy and ownership. This is an exciting time to be a part of this new program.

Position Overview:

Our Principal Biostatisticians provide statistical and development support and influence for the associated client's trials providing expertise into processes, clinical development plans, concept sheets and protocols, as well as potentially providing oversight of work supported by other vendors. You will formulate integrated analytical approach to mine data sources, employ statistical methods, machine learning & deep learning algorithms to discover actionable insights and automate process for reducing effort and time for repeated use.

As a Principal Biostatistician, your responsibilities will include:

  • Lead statistical activities for assigned Clinical Trials (Phases 1 to 4) independently from protocol design to reporting of results.
  • Represent Statistics function on cross-functional trial (and possibly indication / project) teams and collaborate effectively with all cross-functional stakeholders.
  • Oversight of internal programming activities and/or CRO contributions on assigned clinical trials and other activities.
  • Contribute to or lead other activities from a statistical perspective as appropriate, including but not limited to Safety Reporting, ISS/ISE, addressing questions from Health Authorities, Publications.
  • Use SAS and/or R for purposes like QC of datasets and deliverables, inferential statistical analyses, modelling/simulation, exploratory analyses etc.
  • Contribute to and participate in other initiatives at Cytel or sponsor side as appropriate.
  • Oversight of more junior Statisticians as required.
  • Seeking an independent study level lead who
  • has a clear technical understanding of how to analyze clinical trial data properly (ICH E9 guideline)
  • experiences of representing biostats function to collaborate with stakeholders cross functionally
  • is equipped with strong communication skills
  • has a strong self-learning willingness to perform their own duties with minimum guidance.

Here at Cytel we want our employees to succeed and we enable this success through consistent training, development and support. To be successful in this position you will have:

  • Minimum of Bachelor's degree in statistics or a related discipline.
  • 9+ years supporting clinical trials in the Pharmaceutical or Biotechnology industry.
  • Ability to work independently, demonstrate initiative and flexibility through effective and innovative leadership.
  • Attention to detail and quality focused, excellent interpersonal and communication skills, innovative, and collaborative behaviours
  • SAS programming skills for QCing critical outputs, Efficacy/Safety tables, and working closely with Programmers.
  • Knowledge of R programming (R Shiny/Python).

Cytel Inc. is an Equal Employment / Affirmative Action Employer. Applicants are considered for all positions without regard to race, color, religion, sex, national origin, age, veteran status, disability, sexual orientation, gender identity or expression, or any other characteristics protected by law.

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