Senior Statistician II - Biostatistics

Posted 7 Days Ago
Be an Early Applicant
Boston, MA, USA
In-Office
Senior level
Biotech • Pharmaceutical
The Role
Provide biostatistical expertise for complex clinical study design, modelling and simulation, develop statistical analysis plans, perform analyses for regulatory submissions and publications, coach junior statisticians, and improve methodology, quality and delivery across projects.
Summary Generated by Built In

Senior Statistician II 

Location: Boston

The Senior Statistician II has sufficient experience working as a statistician in the pharmaceutical industry to be working independently on activities relating to design, delivery and interpretation, regulatory submissions and/or commercialisation.  This individual is able to perform and communicate results of more technical analyses, and able to guide less experienced staff.  They have the scope to develop creative statistical ideas and approaches, and to apply them in their work.  Competent individual contributor with excellent cross-functional collaboration.  

Typical Accountabilities  

The Senior Statistician II will work directly within a project.   The accountabilities for supporting projects directly are: 

• Provide statistical expertise for complex design and interpretation for clinical programmes, high level internal governance committees, regulatory submissions and/or commercialisation 

• Analyse internal and external information, perform modelling and simulation to inform design decisions and the development of decision criteria 

• Develop a Statistical Analysis plan for complex studies and/or project deliveries 

• Act as a coach/guide for less experienced statisticians in the production of analysis, supporting graphics and analysis tables for study reports, Global Medical Affairs studies or publications 

• Able to analyse, interpret, summarise and communicate results of complex studies 

• Contribute to the regulatory submissions including specification of overview documents and response to regulatory questions 

• Identify opportunities for the application of modelling and simulation to improve study design 

• Identify opportunities to improve the methodology and provide practical solutions for problems 

• Identify and apply statistical methodology to improve the process and delivery activities 

• Contribute to the development of best practice to improve quality, efficiency and effectiveness 

• Accountable for the quality of their statistical work; provide discipline-specific understanding, insight and constructive challenge and take ownership of development needs, seek coaching or training opportunities  

 
Education, Qualifications, Skills and Experience 

Essential 

• MSc/PhD in Statistics, Mathematics (containing a substantial statistical component), or recognised equivalent to stats MSc 

. 3+ yrs experience of pharmaceutical development, data analysis and interpretation.

• Competent statistical programmer (SAS and R) 

• Knowledge of key technical and regulatory requirements 

• Experience of design, analysis and reporting of clinical studies in more than one setting 

• Communication skills 

• Collaboration and team working skills 

• Experience and knowledge of statistical methods and applications in study design, analysis and interpretation   

 
Desirable 

• Collaboration skills required   

• Ability to apply statistical expertise to problems, problem solving and quality focus   

Date Posted

16-Jun-2026

Closing Date

09-Jul-2026

Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.

Skills Required

  • MSc/PhD in Statistics, Mathematics with substantial statistical component, or recognised equivalent
  • 3+ years experience in pharmaceutical development, data analysis and interpretation
  • Competent statistical programmer (SAS and R)
  • Knowledge of key technical and regulatory requirements
  • Experience designing, analysing and reporting clinical studies in more than one setting
  • Experience and knowledge of statistical methods and applications in study design, analysis and interpretation
  • Communication skills
  • Collaboration and team working skills
  • Ability to apply statistical expertise to problems, problem solving and quality focus

AstraZeneca Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about AstraZeneca and has not been reviewed or approved by AstraZeneca.

  • Fair & Transparent Compensation Pay is considered competitive across many roles when total rewards are factored in. Senior scientific and leadership bands are described with high ranges that reinforce competitiveness at upper levels.
  • Strong & Reliable Incentives Bonuses, equity eligibility in many salaried roles, and solid sales on‑target earnings with upside are emphasized as meaningful parts of compensation. These elements boost overall value even where base pay is not the very highest.
  • Retirement Support A 401(k) program with a strong company match and immediate vesting is repeatedly cited as a standout. Generous retirement support is viewed as enhancing the total package relative to peers.

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The Company
HQ: Gaithersburg, MD
70,000 Employees
Year Founded: 1999

What We Do

We're transforming the future of healthcare by unlocking the power of what science can do for people, society and the planet.

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