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Biostatistical Programmer Jobs in Delaware (NOW HIRING)

Cytel

Principal Biostatistician FSP

Dover, DE · On-site

An experienced Principal Biostatistician with a passion for clinical development and analysis ... Oversight of internal programming activities and/or CRO contributions on assigned clinical trials ...

Cytel

Principal Biostatistician FSP

Dover, DE

An experienced Principal Biostatistician with a passion for clinical development and analysis ... Oversight of internal programming activities and/or CRO contributions on assigned clinical trials ...

Prophecy Technologies

R&D CSV Engineer

Wilmington, DE · On-site

The engineer will be responsible for applying core CSV principles and regulatory expertise within a ... High-level understanding of R&D domains such as Biostatistics, Clinical, Discovery, Medical Affairs ...

Zimmer Biomet

$14.25 - $18.75/hr

... to the Biostatistics & Clinical Data Management (BCDM) department in the development and ... Exposure to or coursework in programming languages such as Java, JavaScript, SQL, Python, or ...

Zimmer Biomet

$15 - $20/hr

... to the Biostatistics & Clinical Data Management (BCDM) department in the development and ... Exposure to or coursework in programming languages such as Java, JavaScript, SQL, Python, or ...

Zimmer Biomet

$14.75 - $19.50/hr

... to the Biostatistics & Clinical Data Management (BCDM) department in the development and ... Exposure to or coursework in programming languages such as Java, JavaScript, SQL, Python, or ...

Zimmer Biomet

$13 - $17.50/hr

... to the Biostatistics & Clinical Data Management (BCDM) department in the development and ... Exposure to or coursework in programming languages such as Java, JavaScript, SQL, Python, or ...

Zimmer Biomet

$14.25 - $18.75/hr

... to the Biostatistics & Clinical Data Management (BCDM) department in the development and ... Exposure to or coursework in programming languages such as Java, JavaScript, SQL, Python, or ...

Zimmer Biomet

$14.50 - $19.50/hr

... to the Biostatistics & Clinical Data Management (BCDM) department in the development and ... Exposure to or coursework in programming languages such as Java, JavaScript, SQL, Python, or ...

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Biostatistical Programmer information

What is a biostatistical programmer?

Biostatistical Programmers are professionals who use statistical programming languages, such as SAS, R, or Python, to analyze biological and clinical data. They support clinical trials and public health research by managing datasets, performing statistical analyses, and generating tables, listings, and figures for reports or regulatory submissions. Their work is essential in ensuring data quality and integrity, as well as interpreting results to support scientific conclusions. Biostatistical Programmers often collaborate with statisticians, data managers, and clinical teams in pharmaceutical, biotechnology, or research organizations.

How does a biostatistical programmer typically collaborate with clinical research teams during a study?

Biostatistical Programmers work closely with clinical researchers, data managers, and statisticians throughout the lifecycle of a clinical study. They are responsible for transforming raw clinical trial data into analyzable datasets, generating tables, listings, and figures, and ensuring data integrity. Collaboration often involves participating in regular team meetings to discuss data requirements, timelines, and any challenges that arise during statistical programming. Effective communication and teamwork are essential, as programmers must often clarify statistical analysis plans and adapt to evolving project needs.

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

To thrive as a Biostatistical Programmer, you need a solid background in statistics, programming (typically in SAS, R, or Python), and a relevant degree in biostatistics, mathematics, or a related field. Proficiency with clinical trial data management systems, statistical analysis software, and familiarity with regulatory standards such as CDISC are essential. Attention to detail, problem-solving skills, and effective communication help distinguish top performers in this role. These skills ensure accurate data analysis, regulatory compliance, and clear reporting of clinical trial results, which are critical for advancing medical research.

What cities in Delaware are hiring for Biostatistical Programmer jobs?

Cities in Delaware with the most Biostatistical Programmer job openings:

Principal Biostatistician FSP

Dover, DE • On-site

Cytel
See more jobs at Cytelexternal

Full-time

Posted 12 days ago

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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