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Principal R Jobs (NOW HIRING)

Cytel

An experienced Principal Biostatistician with a passion for clinical development and analysis ... Strong proficiency in R for statistical analyses, simulations, data visualization, and advanced ...

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Principal Attorney (52644)

Poughkeepsie, NY · On-site

$130K/yr

Principal Attorneys may also assist in selecting and training new staff, developing and ... Name Eben R. Hill Telephone Fax Email Address MHLS2-HR@nycourts.gov Address Street 600 Old Country ...

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Principal R information

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$36.5K

$109.4K

$182K

How much do principal r jobs pay per year?

As of Jul 23, 2026, the average yearly pay for principal r in the United States is $109,393.00, according to ZipRecruiter salary data. Most workers in this role earn between $85,000.00 and $125,000.00 per year, depending on experience, location, and employer.

What are Principal R engineers?

Principal R engineers are senior-level professionals who specialize in the R programming language, often leading data science, statistical analysis, or software development projects. They are responsible for designing complex data models, guiding teams, and establishing best practices in coding and analytics. Their role often involves mentoring junior staff, contributing to strategic decision-making, and ensuring high-quality results using R. Principal R engineers are recognized for their expertise in both technical and leadership capacities within organizations.

How does a Principal typically collaborate with teachers and support staff to foster a positive school culture?

Principals play a key role in shaping and maintaining a positive school culture by regularly meeting with teachers and support staff, encouraging open communication, and supporting professional development initiatives. They often facilitate team meetings, provide constructive feedback, and create opportunities for staff to share ideas and best practices. By fostering an environment of trust and collaboration, principals help ensure that everyone works together to create a supportive learning environment for students.

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

To thrive as a Principal, you need strong leadership abilities, educational expertise, and typically a master's degree in education or educational administration along with state certification. Familiarity with school management systems, curriculum planning tools, and data analysis software is often required. Exceptional interpersonal skills, conflict resolution, and the ability to inspire and communicate a clear vision make someone stand out in this role. These skills and qualities are crucial for fostering a positive school environment, driving academic achievement, and effectively managing staff, students, and resources.

What is the difference between Principal R and Senior R Developer?

AspectPrincipal RSenior R Developer
Required CredentialsAdvanced degrees (Master's/PhD), extensive R expertise, leadership skillsTypically bachelor's or master's degree, strong R programming skills
Work EnvironmentLeadership roles, strategic planning, cross-team collaborationProject-focused, coding, data analysis, mentorship
Employer & Industry UsageResearch institutions, large corporations, consulting firmsTech companies, finance, healthcare, analytics firms

The main difference between Principal R and Senior R Developer lies in their responsibilities and experience level. Principal R roles focus on strategic leadership, advanced research, and guiding teams, while Senior R Developers primarily handle complex coding, data analysis, and project execution. Both roles require strong R programming skills, but Principal R positions demand more experience and a broader scope of influence within organizations.

More about Principal R jobs
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What job categories do people searching Principal R jobs look for? The top searched job categories for Principal R jobs are:
Principal R jobs near you
Infographic showing various Principal R job openings in the United States as of July 2026, with employment types broken down into 90% Full Time, 8% Part Time, 1% Temporary, and 1% Contract. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution, with an average salary of $109,393 per year, or $52.6 per hour.
Principal Biostatistician FSP-Must have R proficiency

Principal Biostatistician FSP-Must have R proficiency

Cytel

On-site, Remote

Full-time

Posted 7 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.
Responsibilities
  • Participating in the development of study protocols, including study design discussions and sample size calculations.
  • Participating in exploratory data analyses to evaluate emerging study trends, support scientific decision-making, and generate insights throughout the course of development.
  • Applying advanced statistical methodologies, including mixed models and other complex modeling techniques, to support efficacy and longitudinal analyses.
  • Designing and executing simulation studies to evaluate study designs, operating characteristics, and statistical methodologies.
  • Leading and contributing to efficacy analyses and interpretation of primary and secondary endpoints.
  • Reviewing CRFs and data review guidelines; developing Statistical Analysis Plans (SAPs), including analysis dataset and TLF specifications.
  • Performing statistical analyses and interpreting statistical results.
  • Leading study activities when called upon and providing strategic statistical guidance to cross-functional teams.
  • Utilizing strong communication skills to present statistical methodology, assumptions, and the implications of decisions in clear, non-technical language.
  • Serving as a collaborative team player with a willingness to go the extra distance to meet project goals and timelines.
  • Demonstrating adaptability and flexibility as project priorities evolve.

Qualifications
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:
  • Master's degree in Statistics, Biostatistics, or a related discipline. PhD strongly preferred.
  • 8-10 years of biostatistics experience supporting clinical trials within the pharmaceutical or biotechnology industry. CRO experience strongly preferred.
  • 3-5 years of Study Lead experience working with cross-functional development teams.
  • Extensive experience in study design, sample size determination, protocol development, SAP development, efficacy analyses, and preparation of clinical study reports, including integrated summaries for regulatory submissions (ISS/ISE).
  • Strong knowledge and practical application of advanced statistical methods, including mixed models, longitudinal analyses, and simulation methodologies.
  • Demonstrated experience performing exploratory statistical analyses to support clinical development and decision-making.
  • Strong proficiency in R for statistical analyses, simulations, data visualization, and advanced modeling.
  • Solid SAS programming skills, including QC of critical outputs, efficacy and safety tables, and close collaboration with Statistical Programmers.
  • Strong knowledge of ICH guidelines and regulatory expectations.
  • Solid understanding and implementation of CDISC standards for regulatory submissions.
  • Experience generating ADaM specifications and performing programmatic review of analysis datasets.
  • Regulatory submission experience (ISS/ISE) strongly desired.
  • Excellent communication skills with the ability to explain statistical methodology and its implications to both technical and non-technical audiences.
  • Strong collaborative mindset with a commitment to delivering high-quality work under tight timelines.
  • Ability to thrive in a dynamic environment, manage ambiguity, and adapt to changing priorities.

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