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Statistical Programmer Contract Jobs in Massachusetts

Orion Castings

CMM Programmer

Billerica, MA

$36 - $44/hr

... large-scale, advanced contract manufacturing services worldwide. Operating out of a ... Interpret complex inspection results and statistical data (SPC), communicating variations or ...

campus4tech

Contract System Test Engineer

Newton, MA · On-site

We are currently looking for an ambitious Contract System Test Engineer to join our Endovascular ... on statistical processes • Conducting statistical analysis to determine if multi-sample tests ...

Orion Castings

CMM Programmer

Billerica, MA · On-site

$36 - $44/hr

... large-scale, advanced contract manufacturing services worldwide. Operating out of a ... Interpret complex inspection results and statistical data (SPC), communicating variations or ...

LinQ Global

Safety Data Analyst

Boston, MA · On-site

Boston, MA 02110 Type: 6-Month Contract Job Summary We are seeking a Safety Data Analyst to develop ... Bachelor's degree in Data Analytics, Statistics, Engineering, Safety Management, or a related field ...

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Statistical Programmer Contract information

What is a statistical programmer contract?

A Statistical Programmer Contract refers to a temporary or project-based role where a professional specializes in programming and data analysis, often within clinical research or pharmaceutical industries. These programmers use statistical software like SAS, R, or Python to manage, analyze, and report clinical trial data. Contract positions typically focus on ensuring data integrity, generating tables, listings, and figures, and supporting regulatory submissions. The contract nature means the engagement is for a defined period or project, offering flexibility for both the programmer and the employer.

What are the key skills and qualifications needed to thrive as a statistical programmer contract?

To thrive as a Statistical Programmer Contract, you need a solid background in statistics, programming (especially SAS or R), and a relevant degree in mathematics, statistics, or computer science. Familiarity with statistical software (such as SAS, R, or Python), CDISC standards, and experience with clinical trial datasets are typically required, and certification in SAS programming can be advantageous. Strong analytical thinking, attention to detail, and effective communication skills set top performers apart in this role. These competencies are vital for ensuring the accuracy, integrity, and regulatory compliance of statistical analyses in research or clinical environments.

What are some common challenges faced by statistical programmers working on a contract basis, and how can they be addressed?

Statistical Programmers working on a contract often face challenges such as quickly adapting to new team environments, learning proprietary systems, and managing tight project deadlines. Since contractors may work with multiple clients or projects, strong organizational and communication skills are essential to align with varying expectations and workflows. Building rapport with permanent team members and proactively seeking clarification on project requirements can help smooth the transition and ensure project success.

What are the most commonly searched types of Statistical Programmer jobs in Massachusetts?

The most popular types of Statistical Programmer jobs in Massachusetts are:

What are popular job titles related to Statistical Programmer Contract jobs in Massachusetts?

For Statistical Programmer Contract jobs in Massachusetts, the most frequently searched job titles are:

What job categories do people searching Statistical Programmer Contract jobs in Massachusetts look for?

The top searched job categories for Statistical Programmer Contract jobs in Massachusetts are:

What cities in Massachusetts are hiring for Statistical Programmer Contract jobs?

Cities in Massachusetts with the most Statistical Programmer Contract job openings:

Statistical Programmer Contract jobs near you
Infographic showing various Statistical Programmer Contract job openings in Massachusetts as of August 2026, with employment types broken down into 35% Full Time, and 65% Contract. Highlights an 80% In-person, and 20% Remote job distribution.

Vice President, Biometrics

City Therapeutics

Cambridge, MA • On-site

Full-time

Re-posted 24 days ago

Job description

City Therapeutics is a biopharmaceutical company harnessing next-generation engineering to improve and expand the reach of RNAi-based medicines. The company is building a pipeline of innovative RNAi therapeutics to make a significant impact for patients across multiple therapeutic areas. Co-founded by pioneering executives and scientists in RNAi, City Therapeutics is based in Cambridge, MA, and has raised $140 million from leading life sciences investors.
The Role
The Vice President, Biometrics will serve as the senior leader responsible for biometrics activities at City Therapeutics, encompassing biostatistics, and statistical programming, . This individual will report to CMO and be a key strategic partner to Clinical Development, Clinical Operation, Regulatory Affairs, and Medical Affairs - driving the design, execution, analysis, and reporting of clinical trials across the portfolio.
The VP will establish and scale the Biometrics infrastructure, including internal capabilities, vendor strategy, processes, and systems. This role requires both deep technical expertise and the leadership acumen to influence enterprise-level development decisions, lead related regulatory interactions, and build a high-performing team in a fast-growing organization.
Key Responsibilities
Strategic Leadership & Function Building
  • Define and execute the strategic vision for the Biometrics function, aligning capabilities with City Therapeutics' clinical development goals and pipeline priorities.
  • Build and lead an internal team of biostatisticians, statistical programmers, and data managers; develop hiring plans commensurate with pipeline growth.
  • Establish and continuously improve biometrics processes, SOPs, data standards (CDISC/CDASH/SDTM/ADaM), and quality frameworks.
  • Partner with the CMO, Clinical Development, Clinical Operations and Regulatory Affairs to align biometrics strategy with overall program objectives.

Biostatistics & Statistical Programming
  • Provide statistical leadership and oversight for all clinical trials, including Phase 1-3 and registration studies.
  • Lead the design of clinical trials, including sample size determination, randomization, adaptive design methodology, and endpoint strategy.
  • Author and review Statistical Analysis Plans (SAPs), protocols, and clinical study reports (CSRs) to ensure statistical rigor and regulatory compliance.
  • Drive innovative approaches to trial design, such as seamless adaptive designs, and platform trials where appropriate.
  • Oversee statistical programming teams to ensure accurate, validated, and audit-ready CDISC-compliant datasets (SDTM and ADaM) and TLFs.

Regulatory & Submission Leadership
  • Lead biometrics contributions to global regulatory submissions, including INDs, NDAs, BLAs, MAAs, and agency briefing documents.
  • Represent City Therapeutics Biometrics in interactions with the FDA, EMA, and other health authorities; lead statistical discussions during regulatory meetings.
  • Ensure all deliverables meet regulatory requirements, including 21 CFR Part 11, ICH E9(R1), ICH E6(R2), and applicable FDA/EMA guidance.
  • Provide statistical input for labeling discussions and post-approval commitments.
  • Vendor & Operational Management
  • Develop and manage the CRO and biometrics vendor strategy, including vendor selection, oversight, and performance management.
  • Negotiate contracts and oversee budgets for all outsourced biometrics activities.
  • Implement risk-based quality oversight frameworks to ensure high-quality, on-time delivery by external partners.
  • Collaborate closely with Clinical Development, Clinical Operations, Medical Affairs, Translational Medicine, and Commercial to support data-driven decision-making across the organization.
  • Contribute to business development activities, including target assessment, due diligence, and partnership evaluations requiring quantitative analysis.
  • Represent Biometrics at governance committees, portfolio reviews, and executive leadership meetings.

Qualifications
  • PhD, MS, or equivalent advanced degree in Biostatistics, Statistics, or a closely related quantitative field.
  • Minimum of 12 years of experience in biometrics within the pharmaceutical or biopharmaceutical industry, with at least 5 years in a senior leadership role overseeing biostatistics, programming, and/or data management.
  • Demonstrated success leading biometrics for at least one NDA, BLA, or equivalent global regulatory submission resulting in approval.
  • Deep expertise in clinical trial design (including adaptive designs), statistical methodology, and regulatory statistics (ICH E9, E9(R1), E8).
  • Extensive experience with CDISC standards (CDASH, SDTM, ADaM) and regulatory submission requirements.
  • Proven track record building and leading high-performing biometrics teams, internally and through CRO partnerships.
  • Strong experience with FDA, EMA, and global health authority interactions on statistical matters.
  • Proficiency in SAS; experience with R and other programming languages a plus.
  • Exceptional communication skills with the ability to translate complex statistical concepts for non-statistical audiences.

Compensation
The base salary range provided reflects our current estimate of what we anticipate paying for this position. Your actual base salary will be based on several factors, including job-related skills, experience, internal equity, relevant education or training, and market dynamics. In addition, you will be eligible for an annual bonus, equity compensation, and a competitive benefits package. Pay range is $311,000 to $360,000
Our Working Model: In Person, By Design
At City, we believe that science and culture thrive together, and that happens best in person. Our working model is clear: we work onsite at our Kendall Square offices five days per week.
This choice reflects our belief that great science and cultures run on connection, fairness, and growth.
• Connection: Face time matters. Building an enduring biotech company is about people, science, and strategy. Working side by side sharpens ideas, accelerates feedback, and fuels innovation for patients.
• Fairness: One model for all. Every voice counts, and fairness depends on shared experience. We hold ourselves to one standard across all levels and functions.
• Growth: Learning moves faster in person. Growth comes from conversation, observation, and mentorship. We believe in developing talent, and that happens best when we're together.
We also know that life isn't always predictable. When individual needs arise, we're flexible and supportive and work together to balance home life with life at City.
We believe diverse teams drive better science. We welcome applicants from all backgrounds and experiences who share our mission to bring transformative RNAi medicines to patients.
City Therapeutics is an Equal Opportunity and Affirmative Action employer. All qualified applicants will receive consideration without regard to race, color, religion, national origin, gender, gender identity or expression, sexual orientation, age, disability, veteran status, or any other characteristic protected by law.
City Therapeutics is accepting applications from direct candidates only. Agency inquiries or submissions will not be accepted at this time.

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