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Senior Statistical Programmer Jobs in Lowell, MA

Job Summary The Chai Laboratory seeks a doctoral-level Senior Computational Scientist to provide ... Qualifications Education Master's Degree Statistics required or Master's Degree Related Field of ...

Biostatistician Principal

Boston, MA · On-site

$56.59 - $82.31/hr

Job Summary The Chai Laboratory seeks a doctoral-level Senior Computational Scientist to provide ... Qualifications Education Master's Degree Statistics required or Master's Degree Related Field of ...

Programming and conducting statistical analysis under the direction and supervision of epidemiologists/statisticians including data coding, creation of algorithms, linkage of datasets, and use of ...

As a Senior Biostatistician you will be dedicated to one of our global pharmaceutical clients; a ... Provide review and/or author SOPs and/or Work Instructions related to statistical programming ...

New

Showing results 41-60

Senior Statistical Programmer information

See Lowell, MA salary details

$81.8K

$127.2K

$166.1K

How much do senior statistical programmer jobs pay per year?

As of Sep 3, 2026, the average yearly pay for senior statistical programmer in Lowell, MA is $127,237.00, according to ZipRecruiter salary data. Most workers in this role earn between $106,100.00 and $146,800.00 per year, depending on experience, location, and employer.

What is a senior statistical programmer?

A Senior Statistical Programmer is responsible for developing, testing, and validating statistical programs used for clinical trial data analysis. They work primarily with statistical software like SAS to generate tables, listings, and figures (TLFs) for regulatory submissions and research studies. This role requires strong programming skills, knowledge of statistical methodologies, and an understanding of clinical trial processes. Senior Statistical Programmers also collaborate with statisticians, data managers, and regulatory teams to ensure data integrity and compliance with industry standards.

What are the typical responsibilities and team dynamics for a senior statistical programmer?

As a Senior Statistical Programmer, you will typically be responsible for designing, developing, and validating statistical programs for clinical trial data analysis and reporting. You’ll work closely with biostatisticians, data managers, and clinical project teams to ensure data quality and regulatory compliance, often contributing to the creation of submission datasets and study reports. The role usually involves both independent work and active collaboration, with seasoned programmers frequently mentoring junior staff and participating in process improvement initiatives. This team-oriented structure offers exposure to a variety of projects and stakeholders, making it a dynamic environment ideal for those who enjoy both analytical tasks and cross-functional teamwork.

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

To thrive as a Senior Statistical Programmer, a strong background in statistical analysis, programming (often in SAS and R), and a relevant degree such as in statistics, mathematics, or computer science is essential. Experience with regulatory submission standards (like CDISC SDTM/ADaM), clinical trial software, and certifications such as SAS Certified Advanced Programmer are highly valued. Outstanding attention to detail, problem-solving abilities, and effective communication skills help individuals excel in this collaborative and deadline-driven role. These skills are crucial for ensuring accurate data analysis, regulatory compliance, and successful teamwork in high-stakes research environments.

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The top searched job categories for Senior Statistical Programmer jobs in Lowell, MA are:

What cities near Lowell, MA are hiring for Senior Statistical Programmer jobs?

Cities near Lowell, MA with the most Senior Statistical Programmer job openings:

Infographic showing various Senior Statistical Programmer job openings in Lowell, MA as of August 2026, with employment types broken down into 1% Internship, 79% Full Time, 16% Part Time, and 4% Contract. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution, with an average salary of $127,237 per year, or $61.2 per hour.

Senior Director, Statistical Programming

Bicycle Therapeutics

Lexington, MA • On-site

$97K - $119K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 19 days ago


Job description

Company Description

About Bicycle Therapeutics 

Bicycle Therapeutics is a clinical-stage pharmaceutical company developing a novel class of medicines, referred to as Bicycle® molecules, for diseases that are underserved by existing therapeutics. Bicycle molecules are fully synthetic short peptides constrained with small molecule scaffolds to form two loops that stabilize their structural geometry. This constraint facilitates target binding with high affinity and selectivity, making Bicycle® molecules attractive candidates for drug development. The company is evaluating nuzafatide pevedotin (formerly BT5528), a Bicycle® Drug Conjugate (BDC®) targeting EphA2, a historically undruggable target; a pipeline of Bicycle® Radioconjugates (BRCs) and imaging agents; zelenectide pevedotin (formerly BT8009), a BDC® targeting Nectin-4, a well-validated tumor antigen; and, through various partnerships, the use of Bicycle® technology to develop therapies to treat diseases in a range of therapeutic areas.

Bicycle Therapeutics is headquartered in Cambridge, UK, with many key functions and members of its leadership team located in Lexington, Massachusetts, USA. For more information, visit bicycletherapeutics.com 

Culture is key and all Bicycle employees actively embrace and role model our company values:

  • We are Adventurous. We believe it’s the way to deliver extraordinary results for our patients.  
  • We are Dedicated to our Mission. You can’t change the world if you don’t have determination.
  • We are One Team. We only succeed when we work together. 

Working Classification:

At Bicycle, we benefit from a hybrid style working arrangement, allowing employees where possible the opportunity to collaborate and engage with their coworkers in person while also benefiting from the flexibility of remote working. A typical hybrid arrangement for this role is 2-3 days onsite per week at our Lexington, MA office, with the remainder of your working week remote.

Job Description

Your mission is to provide strategic and technical leadership for the statistical programming function, driving the delivery of high-quality data and analysis for Bicycle's clinical portfolio. You will ensure operational excellence across all programming activities, serve as a key strategic partner to Biostatistics and Clinical Development, and lead and mentor a team of programmers to support the successful execution of our clinical trials and regulatory submissions.

YOUR RESPONSIBILITIES  

Strategic & Technical Leadership

  • Provide strategic leadership and hold accountability for all statistical programming deliverables for assigned clinical development programs, ensuring timelines, quality, and compliance are met.
  • Serve as the senior technical expert on CDISC standards (SDTM, ADaM), programming methodologies, and data submission strategies, guiding the team and vendors on complex implementation challenges.
  • Partner with the Biometrics Lead to define and execute the long-term vision and strategy for the statistical programming function, including resource planning, technology adoption, and talent development.

Operational Excellence & Process Innovation

  • Drive the strategy for functional excellence by developing, implementing, and optimizing global Standard Operating Procedures (SOPs), tools, and innovative workflows to enhance efficiency and quality.
  • Oversee the strategic selection and governance of CROs and external vendors, ensuring a harmonized approach to programming and holding partners accountable for high-quality, timely deliverables.
  • Ensure all statistical programming activities and documentation are inspection-ready, providing senior oversight for data integrity and demonstrable compliance with ICH/GCP guidelines.

Team Leadership & Development

  • You will lead, coach, and mentor your team, investing in their professional growth and fostering a culture of high performance and psychological safety.
  • You will set clear goals and strategic priorities for your team, ensuring their work is directly aligned with departmental and organisational objectives.
  • You will champion the Bicycle Values in all that you do, acting as a role model and embedding a culture of collaboration, accountability, and innovation within your team.

WHO ARE YOU: SKILLS & COMPETENCIES

Knowledge:

  • You apply expert knowledge of statistical programming and clinical development to set functional strategy and solve complex, multi-faceted problems. You have a deep understanding of the regulatory landscape and its impact on programming deliverables.

Job Complexity:

  • You are accountable for managing a portfolio of complex clinical programs and addressing abstract challenges that require in-depth evaluation of variable factors. You anticipate future needs and develop innovative, long-range solutions for the programming function.

Independence:

  • You operate with a high degree of independence, aligning your team's strategy with broader departmental and company goals. You are trusted to make significant decisions regarding project execution, resource allocation, and vendor management.

Values & Behaviours:

  • You are a role model for the Bicycle Values, leading by example to create an inclusive and high-performing team environment. You build strong, influential relationships with senior stakeholders across the organization and represent the function with credibility.
Qualifications
  • Demonstrated deep expertise in statistical programming gained through significant and progressive experience in a biotech or pharmaceutical setting.
  • Proven track record of leading the programming strategy for clinical development programs, preferably within oncology.
  • Expert-level knowledge of SAS programming and CDISC data standards (SDTM/ADaM), with extensive experience preparing data for regulatory submissions (e.g., NDA/BLA).
  • Substantial experience in managing CROs and external vendors, including technical oversight, governance, and relationship management.
  • Proven leadership experience, with the ability to mentor programmers, set strategic direction for a team, and influence cross-functional partners.

Additional Information
  • 401(k) plan with a 4% Company match and immediate vesting 
  • Medical, dental, and vision insurance for eligible employees and their families with 100% of the premiums covered by the Company 
  • Health and Dependent Care Flexible Spending Accounts 
  • Employee assistance program (EAP)
  • Time off (eligibility to accrue up to 23 paid time off days per full year worked, the option to buy up to 5 additional days & 10 company nominated holidays)
  • 10 Company holidays 
  • Competitive reward including annual company bonus 
  • Employee recognition schemes
  • Enhanced parental leave policies
  • Flexible working environment
  • Eligibility for an option grant to subscribe to shares in Bicycle Therapeutics plc. 

Compensation

  • Salary Range: $215,000 - $270,000

Bicycle Therapeutics is committed to building a diverse workforce that is representative of the communities we serve. We recognize that diverse and inclusive teams build a stronger and more innovative company. Therefore, all qualified applicants will be considered for employment, and we do not discriminate on the basis of race, religion, colour, gender, sexual orientation, age, disability status, marital status, or veteran status.