In this role, you will lead study-level statistical programming deliverables, including developing ... The current base salary range for this Senior Manager position is expected to be between $131,035 ...
In this role, you will lead study-level statistical programming deliverables, including developing ... The current base salary range for this Senior Manager position is expected to be between $131,035 ...
The Biometrics Quality Team provides leadership and support for the Global Biometrics department, which consists of Data Management, Biostatistics and Statistical Programming. The Sr. Associate ...
The Biometrics Quality Team provides leadership and support for the Global Biometrics department, which consists of Data Management, Biostatistics and Statistical Programming. The Sr. Associate ...
Director, Biostatistics
Boston, MA · On-site
$230K - $265K/yr
... management for biostatistics and programming services Cross-Functional & Regulatory Engagement * Partner closely with Clinical Development to ensure statistical approaches align with program ...
Director, Biostatistics
Boston, MA · On-site
$230K - $265K/yr
... management for biostatistics and programming services Cross-Functional & Regulatory Engagement * Partner closely with Clinical Development to ensure statistical approaches align with program ...
Director, Biostatistics
Boston, MA · On-site
... management for biostatistics and programming services CrossFunctional & Regulatory Engagement * Partner closely with Clinical Development to ensure statistical approaches align with program ...
Director, Biostatistics
Boston, MA · On-site
... management for biostatistics and programming services CrossFunctional & Regulatory Engagement * Partner closely with Clinical Development to ensure statistical approaches align with program ...
Director, Biostatistics
$230K - $265K/yr
... management for biostatistics and programming services CrossFunctional & Regulatory Engagement * Partner closely with Clinical Development to ensure statistical approaches align with program ...
Director, Biostatistics
$230K - $265K/yr
... management for biostatistics and programming services CrossFunctional & Regulatory Engagement * Partner closely with Clinical Development to ensure statistical approaches align with program ...
Head of Biometrics
$310K - $395K/yr
Manage the statistical programming function and ensure delivery of high-quality datasets and analysis outputs in support of study reports, submissions, and publications. * Build and lead a high ...
Head of Biometrics
$310K - $395K/yr
Manage the statistical programming function and ensure delivery of high-quality datasets and analysis outputs in support of study reports, submissions, and publications. * Build and lead a high ...
Experience managing CRO statistical and programming relationships and vendor deliverable quality. * Proficiencyin SAS (required); R strongly preferred; Python or additional statistical languages a ...
Experience managing CRO statistical and programming relationships and vendor deliverable quality. * Proficiencyin SAS (required); R strongly preferred; Python or additional statistical languages a ...
Head of Biometrics
Watertown, MA · On-site
$310K - $395K/yr
Manage the statistical programming function and ensure delivery of high-quality datasets and analysis outputs in support of study reports, submissions, and publications. * Build and lead a high ...
Head of Biometrics
Watertown, MA · On-site
$310K - $395K/yr
Manage the statistical programming function and ensure delivery of high-quality datasets and analysis outputs in support of study reports, submissions, and publications. * Build and lead a high ...
Programming and conducting statistical analysis under the direction and supervision of ... Global Patient Safety and Risk Management (e.g., analysis to obtain background rates) for the ...
Programming and conducting statistical analysis under the direction and supervision of ... Global Patient Safety and Risk Management (e.g., analysis to obtain background rates) for the ...
Principal Statistical Programmer
Boston, MA · On-site
$149K - $223K/yr
The Principal Statistical Programmer works with management to delegate tasks appropriately, track progress, and provide expert technical support to team members. In addition, the Principal ...
Principal Statistical Programmer
Boston, MA · On-site
$149K - $223K/yr
The Principal Statistical Programmer works with management to delegate tasks appropriately, track progress, and provide expert technical support to team members. In addition, the Principal ...
Principal Statistical Programmer
Boston, MA · Remote
$149K - $223K/yr
The Principal Statistical Programmer works with management to delegate tasks appropriately, track progress, and provide expert technical support to team members. In addition, the Principal ...
Principal Statistical Programmer
Boston, MA · Remote
$149K - $223K/yr
The Principal Statistical Programmer works with management to delegate tasks appropriately, track progress, and provide expert technical support to team members. In addition, the Principal ...
Basic knowledge of statistical analysis methodologies and study design concepts * Fundamentals of project planning and management * Drug development process Communication & Interpersonal Skills:
Basic knowledge of statistical analysis methodologies and study design concepts * Fundamentals of project planning and management * Drug development process Communication & Interpersonal Skills:
Basic knowledge of statistical analysis methodologies and study design concepts * Fundamentals of project planning and management * Drug development process Communication & Interpersonal Skills:
Basic knowledge of statistical analysis methodologies and study design concepts * Fundamentals of project planning and management * Drug development process Communication & Interpersonal Skills:
Senior EDC Programmer (Medidata)
Cambridge, MA · On-site +1
Act as a liaison between Data Management and Statistical Programming to ensure data collection strategies support downstream analysis, reporting, and regulatory submission requirements. * Collaborate ...
Senior EDC Programmer (Medidata)
Cambridge, MA · On-site +1
Act as a liaison between Data Management and Statistical Programming to ensure data collection strategies support downstream analysis, reporting, and regulatory submission requirements. * Collaborate ...
Senior EDC Programmer (Medidata)
Cambridge, MA · On-site +1
Act as a liaison between Data Management and Statistical Programming to ensure data collection strategies support downstream analysis, reporting, and regulatory submission requirements. * Collaborate ...
Senior EDC Programmer (Medidata)
Cambridge, MA · On-site +1
Act as a liaison between Data Management and Statistical Programming to ensure data collection strategies support downstream analysis, reporting, and regulatory submission requirements. * Collaborate ...
... statistical reports for project queries. • Utilization of various database management tools and systems. • Based on level of experience, may also assist Biostatistical lead in the programming ...
... statistical reports for project queries. • Utilization of various database management tools and systems. • Based on level of experience, may also assist Biostatistical lead in the programming ...
Create, manage and maintain the programmingspecifications for the analysis datasets utilizing ... Provide programming support for simple presentations and basic statistical ad-hoc requests. Assist ...
Create, manage and maintain the programmingspecifications for the analysis datasets utilizing ... Provide programming support for simple presentations and basic statistical ad-hoc requests. Assist ...
Director, Biostatistics (Oncology)
Cambridge, MA · On-site
$168K - $268K/yr
Provide input to database requirements and work closely with Clinical Data Manager to ensure data quality standards are met * Provide guidance to Statistical Programmers on SDTM/ADaM and TLFs ...
Director, Biostatistics (Oncology)
Cambridge, MA · On-site
$168K - $268K/yr
Provide input to database requirements and work closely with Clinical Data Manager to ensure data quality standards are met * Provide guidance to Statistical Programmers on SDTM/ADaM and TLFs ...
Director, Biostatistics (Oncology)
Cambridge, MA · On-site +1
$168K - $268K/yr
Provide input to database requirements and work closely with Clinical Data Manager to ensure data quality standards are met * Provide guidance to Statistical Programmers on SDTM/ADaM and TLFs ...
Director, Biostatistics (Oncology)
Cambridge, MA · On-site +1
$168K - $268K/yr
Provide input to database requirements and work closely with Clinical Data Manager to ensure data quality standards are met * Provide guidance to Statistical Programmers on SDTM/ADaM and TLFs ...
Lead Clinical Programmer
Boston, MA · On-site
... including Data Management and GPS, to understand requirements for non-statistical clinical ... This position is responsible for taking a lead role in SAS programming support of centralized ...
Lead Clinical Programmer
Boston, MA · On-site
... including Data Management and GPS, to understand requirements for non-statistical clinical ... This position is responsible for taking a lead role in SAS programming support of centralized ...
Manager Statistical Programming information
See Lexington, MA salary details
$94.9K - $111.7K
3% of jobs
$111.7K - $128.5K
10% of jobs
$139.9K is the 25th percentile. Wages below this are outliers.
$128.5K - $145.3K
18% of jobs
The median wage is $162.1K / yr.
$145.3K - $162.1K
19% of jobs
$176.8K is the 75th percentile. Wages above this are outliers.
$162.1K - $178.9K
29% of jobs
$178.9K - $195.8K
10% of jobs
$195.8K - $212.6K
12% of jobs
$212.6K - $229.4K
0% of jobs
$229.4K - $246.2K
0% of jobs
$246.2K - $263K
0% of jobs
$263K - $279.8K
0% of jobs
$94.9K
$165.5K
$279.8K
How much do manager statistical programming jobs pay per year?
What is a Manager Statistical Programming job?
A Manager Statistical Programming oversees a team of statistical programmers who support clinical trials and research by developing, validating, and maintaining statistical programs. They ensure compliance with regulatory requirements, manage project timelines, and collaborate with statisticians, data managers, and other stakeholders. This role requires strong programming skills in SAS or other statistical software, leadership abilities, and expertise in clinical data standards such as CDISC.
What are the typical daily responsibilities of a Manager Statistical Programming?
As a Manager Statistical Programming, your daily responsibilities usually include overseeing a team of statistical programmers, coordinating the development and validation of statistical programs for clinical trial data analysis, and ensuring deliverables meet regulatory and company quality standards. You will often interact with biostatisticians, data managers, and clinical teams to align programming outputs with study goals. Additionally, you may review project timelines, allocate resources, mentor junior programmers, and contribute to process improvement initiatives. This multifaceted role requires balancing technical oversight with leadership and interdepartmental communication.
What are the key skills and qualifications needed to thrive in the Manager Statistical Programming position, and why are they important?
To excel as a Manager Statistical Programming, you need a solid background in statistics, programming (such as SAS, R, or Python), and experience with clinical trial data management, often supported by a degree in statistics, mathematics, or a related field. Familiarity with regulatory guidelines (e.g., FDA, ICH), data standards such as CDISC, and certifications in relevant programming languages or clinical data processes are highly beneficial. Strong leadership, project management, and effective communication skills are essential for guiding teams and collaborating with cross-functional departments. These skills enable the manager to deliver high-quality statistical programming deliverables, ensure regulatory compliance, and drive team performance in a deadline-driven environment.

Principal Statistical Programmer, Biometrics
Agios Pharmaceuticals IncCambridge, MA • On-site, Remote
Full-time
Posted 7 days ago
Job description
Principal Statistical Programmer, Biometrics
Who we are:
At Agios, we are fueled by connections to transform rare diseases. We foster an inclusive, collaborative culture - one that sparks bold thinking and strengthens our connections with each other and with the rare disease communities we serve. We embrace diverse backgrounds with respect, active listening, and a commitment to inclusion - because our differences shape how we hire, collaborate, and innovate. Our team's proven track record of executional excellence, combined with our depth of expertise and dedication, enables us to develop innovative medicines that reflect the priorities of rare disease communities. Our commitment is more than scientific - it's deeply personal, grounded in the meaningful connections we have built. To learn more, visit www.agios.com and follow Agios on LinkedIn and X.
The impact you will make:
Agios Pharmaceuticals is seeking a dynamic Principal Statistical Programmer to join our growing Biometrics team. We are looking for someone who is passionate about this work and motivated by our mission to serve patient communities. In this role, you will lead study-level statistical programming deliverables, including developing programming specifications and programs for SDTMs and analysis datasets in accordance with Agios, CDISC, and study- or submission-specific standards; develop programs for tables, listings, and figures based on Agios standards or study-specific/submission-specific requirements, reviewing CRFs and creating SDTM-annotated CRFs; reviewing statistical analysis plans, analysis datasets, and outputs; performing hands-on programming; and reviewing CRO deliverables. Candidate must have a strong working knowledge of CDISC requirements and Pinnacle 21.
What you will do:
- Develop and/or validate programming specifications and programs to generate SDTMs and analysis datasets, using Agios, CDISC standards and study-specific/submission-specific requirements.
- Develop and/or validate specifications and programs to generate tables, listings, and figures based on Agios standards and study-specific/submission-specific requirements.
- Create SDTM-annotated CRFs
- Accountable for study-level statistical programming deliverables on assigned projects, including timeliness and quality of deliverables.
- Review statistical analyses plans and case report forms.
- Ensure documentation is maintained to the standard required according to CDISC-compliant submissions and is acceptable for audit.
- Support establishment and maintenance of statistical programming standards at Agios.
- Ensure that all study-level statistical programming activities are conducted in compliance with relevant regulatory requirements, Agios SOPs and Agios standards.
- Serve as a general statistical programming resource at Agios including representation in cross-functional teams working on standard operating procedures, guidelines, process improvements, system validation and acquisition, customization, and integration of new tools and technologies.
What you bring:
- MS or equivalent degree with 7+ years biopharmaceutical industry experience
- 3+ years project management experience as a statistical programmer preferred
- Advanced knowledge of SAS/Base, SAS/Macro, SAS/STAT, SAS/Graph, and SAS/SQL in a windows environment
- Extensive experience and proven skills in the use of SAS within a Statistical Programming environment to develop and validate analysis datasets, tables, listings, and figures
- Hands-on experience on SDTM mapping from various data sources
- Knowledge of clinical database design, specifically electronic data capture using Rave, Veeva, and Medidata
- Experience supporting electronic submissions in the eCTD format
- Excellent oral and written communication skills
- Experience in open-source languages like Python or R preferred
Concerned that you don't check off every box in the requirements listed above? Please apply anyway! At Agios, we value each other's differences and recognize that teams thrive when everyone brings their unique experiences to the table. We are dedicated to building an inclusive, diverse, equitable, and accessible environment where all employees can bring their whole selves to work. If you're excited about this role but your previous experience doesn't align perfectly with the job description, we still encourage you to apply. You may be just the right candidate for this role or another opening!
Work Location:
Location Agnostic: Work location for this role is based on employee's individual preference. This role has the ability to be either remote in the US or hybrid in our Cambridge Headquarters. Hybrid schedules vary but are generally less than 3 days per week onsite and hybrid employees are expected to live within commutable distance to our Cambridge Headquarters. Remote employees work entirely from home except for attending Company sponsored events/ meetings. For employees who choose to work remotely, travel may be required for certain company events commensurate to the above job description.
What we will give you:
- Deliberate Development. Your professional growth as one of our top priorities.
- Flexibility. We're all about individual needs. We embrace different perspectives, work styles, health and wellness approaches, care of families and productivity. When you're at your best, we're at our best.
- Premium benefits package. We invest in the health, wellbeing, and security of our people with a premium benefits package that is well-rounded and flexible to help meet the varied personal and professional needs of every member of our team. For more detail on the benefits we offer at Agios, visit the Inside Agios section of our website.
- Competitive and equitable performance-based compensation. This includes base salary and both short- and long-term incentives that are connected to our business strategy and vary based on individual and company performance.
- The current base salary range for this Senior Manager position is expected to be between $131,035 and $196,553 annualized; final salary will be determined based on various factors including, but not limited to, years of relevant experience, job knowledge, skills and proficiency, degree/education, and internal comparators.
- Psychological safety. We support an environment of fearlessness. We want you to share your ideas, speak candidly and take data-informed risks to help push the boundaries.
- Commitment to diversity. We strive to foster a welcoming workplace where everyone can thrive. We're continuously looking to improve the inclusivity of our workforce.
- Commitment to community. We're an active participant in the communities that surround us - the communities where we live, and the community of people and their loved ones in need of better treatment options for conditions that are often overlooked.
Interested in learning more about what makes our culture unique? Visit the Inside Agios section of our website.
Employment Type: Full timeAbout Agios Pharmaceuticals
Sourced by ZipRecruiter
Industry
Pharmaceutical and medicine manufacturing
Company size
201 - 500 Employees
Headquarters location
Cambridge, MA, US
Year founded
2008