Statistical Science Director
Location: Boston, MA
The Statistical Science Director has sufficient experience working as a statistician in the pharmaceutical industry to be accountable and independently lead the statistical strategy or technical activities related to design, delivery and interpretation, high level internal governance committees and/or regulatory submissions of a project. This individual is able to lead, perform and communicate results of more technical analyses, and able to guide less experienced staff. Competent individual contributor with excellent cross-functional collaboration.
Typical Accountabilities:
Lead the statistical design and strategy to product development plans, clinical studies, regulatory strategy, health technology assessment and/or commercial activities as appropriate for the stage of the product
Lead the statistical content and ensure quality for study designs, documents, delivery and interpretation and submission
Quantify the benefit, risk, value and uncertainty of the emerging product profile and can communicate these effectively within the team
Provide global leadership to others and direct project work delivered by internal and external staff
Partner with CROs to ensure delivery to quality and time
Represent AZ externally which may include health authorities, advisory boards, conferences, workshops and/or payer interactions
Maintain knowledge of statistical methodology in relevant areas and promote, investigate and implement novel statistical approaches
Represent statistical strategy and decision making at internal decision-making governance including review boards, therapy area leadership teams and internal governance committees
Mentor/coach and support the technical education and training of Statistics staff
Education, Qualifications, Skills and Experience: Essential:
MSc/PhD in Statistics, Mathematics (containing a substantial statistical component), or recognised equivalent to stats MSc
7+ yrs of experience of pharmaceutical development, data analysis and interpretation and experience of program design.
Track record of background in leading independently
Experience with and broad awareness of regulatory interactions and/or submissions
Exemplary technical skills
Excellent communication skills/ builds strong relationships
Desirable:
TA or disease area knowledge expertise
Exposure to business development opportunities (e.g.in licencing)
Project management skills
Proficiency in programming SAS and/or R and Python
The annual base pay for this position ranges from $188,000 to $282,000. Our positions offer eligibility for various incentives—an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans.
Date Posted
12-Feb-2026
Closing Date
27-Feb-2026
AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.
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.
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Location: Boston, MA
The Statistical Science Director has sufficient experience working as a statistician in the pharmaceutical industry to be accountable and independently lead the statistical strategy or technical activities related to design, delivery and interpretation, high level internal governance committees and/or regulatory submissions of a project. This individual is able to lead, perform and communicate results of more technical analyses, and able to guide less experienced staff. Competent individual contributor with excellent cross-functional collaboration.
Typical Accountabilities:
Lead the statistical design and strategy to product development plans, clinical studies, regulatory strategy, health technology assessment and/or commercial activities as appropriate for the stage of the product
Lead the statistical content and ensure quality for study designs, documents, delivery and interpretation and submission
Quantify the benefit, risk, value and uncertainty of the emerging product profile and can communicate these effectively within the team
Provide global leadership to others and direct project work delivered by internal and external staff
Partner with CROs to ensure delivery to quality and time
Represent AZ externally which may include health authorities, advisory boards, conferences, workshops and/or payer interactions
Maintain knowledge of statistical methodology in relevant areas and promote, investigate and implement novel statistical approaches
Represent statistical strategy and decision making at internal decision-making governance including review boards, therapy area leadership teams and internal governance committees
Mentor/coach and support the technical education and training of Statistics staff
Education, Qualifications, Skills and Experience: Essential:
MSc/PhD in Statistics, Mathematics (containing a substantial statistical component), or recognised equivalent to stats MSc
7+ yrs of experience of pharmaceutical development, data analysis and interpretation and experience of program design.
Track record of background in leading independently
Experience with and broad awareness of regulatory interactions and/or submissions
Exemplary technical skills
Excellent communication skills/ builds strong relationships
Desirable:
TA or disease area knowledge expertise
Exposure to business development opportunities (e.g.in licencing)
Project management skills
Proficiency in programming SAS and/or R and Python
The annual base pay for this position ranges from $188,000 to $282,000. Our positions offer eligibility for various incentives—an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans.
Date Posted
12-Feb-2026
Closing Date
27-Feb-2026
AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.
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.
#J-18808-Ljbffr