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Associate Director Statistical Programming Jobs in Cambridge, MA

Head of Biometrics

Watertown, MA · On-site

$310K - $395K/yr

In your role as Head of Biometrics , you will be responsible for leading all biostatistics and statistical programming activities across Treeline's clinical and translational development programs.

Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a dynamic customer project focused on AI-assisted clinical research. In this role, you'll apply your ...

Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a dynamic customer project focused on AI-assisted clinical research. In this role, you'll apply your ...

Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a dynamic customer project focused on AI-assisted clinical research. In this role, you'll apply your ...

Director of Biostatistics

Lynn, MA · Remote

$60 - $65/hr

Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a dynamic customer project focused on AI-assisted clinical research. In this role, you'll apply your ...

Head of Biometrics

Watertown, MA · On-site

$310K - $395K/yr

Manage the statistical programming function and ensure delivery of high-quality datasets and ... agreement directed to the particular position or positions is in place at the start of the ...

Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a dynamic customer project focused on AI-assisted clinical research. In this role, you'll apply your ...

Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a dynamic customer project focused on AI-assisted clinical research. In this role, you'll apply your ...

Biostatistics Associate Director (HYBRID)

Boston, MA · Hybrid

$174K - $262K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Biostatistics Associate Director will perform sophisticated scientific statistical analyses in ... Collaborates with statistical programming and other functions to ensure timely delivery of TFLs ...

Showing results 41-60

Associate Director Statistical Programming information

See Cambridge, MA salary details

$167.8K

$306.2K

$376K

How much do associate director statistical programming jobs pay per year?

As of Aug 18, 2026, the average yearly pay for associate director statistical programming in Cambridge, MA is $306,194.00, according to ZipRecruiter salary data. Most workers in this role earn between $284,700.00 and $352,500.00 per year, depending on experience, location, and employer.

What does an associate director statistical programming do?

An Associate Director of Statistical Programming leads teams responsible for the design, development, and validation of statistical programs used in the analysis of clinical trial data. They oversee the creation of datasets, tables, listings, and figures that support regulatory submissions and scientific publications. In addition to technical expertise, this role involves managing timelines, ensuring compliance with regulatory standards, and collaborating with cross-functional teams such as biostatistics, data management, and clinical operations.

What are the key skills and qualifications needed to thrive as an associate director statistical programming?

To thrive as an Associate Director Statistical Programming, you need expertise in statistical programming, clinical trial data standards, and a degree in statistics, mathematics, or a related field, often with several years of experience in the pharmaceutical or biotechnology industry. Proficiency in programming languages such as SAS and R, knowledge of CDISC standards (SDTM, ADaM), and familiarity with regulatory submission requirements are typically required. Strong leadership, project management, and communication skills are vital for guiding teams and collaborating with cross-functional partners. These skills and qualities ensure the delivery of high-quality, compliant statistical outputs that support clinical development and regulatory approval.

How does an associate director statistical programming typically collaborate with cross-functional teams in a pharmaceutical or biotech setting?

As an Associate Director of Statistical Programming, you will work closely with biostatisticians, clinical data managers, and regulatory affairs professionals to ensure that statistical analyses and data outputs meet project and regulatory requirements. You’ll often lead programming teams, coordinate timelines, and help translate statistical analysis plans into executable code. Regular meetings and clear communication are key, as you’ll be expected to provide technical guidance and ensure data integrity across multiple studies or programs. This role often requires balancing hands-on programming with strategic leadership and mentorship responsibilities.

What is the difference between Associate Director Statistical Programming vs Statistical Programmer?

AspectAssociate Director Statistical ProgrammingStatistical Programmer
Required CredentialsBachelor's or Master's in Biostatistics, Statistics, or related field; experience in clinical trial programmingBachelor's or Master's in similar fields; entry to mid-level experience
Work EnvironmentLeads teams, manages projects, collaborates with cross-functional teamsPerforms programming tasks, supports project teams, executes statistical analyses
Employer & Industry UsagePharmaceutical and biotech companies, clinical research organizationsPharmaceutical companies, CROs, biotech firms

The Associate Director Statistical Programming typically oversees programming teams and manages project deliverables, requiring leadership skills and extensive experience. In contrast, the Statistical Programmer focuses on executing programming tasks under supervision. Both roles are essential in clinical research, but the Associate Director holds more managerial responsibilities and strategic oversight.

What are popular job titles related to Associate Director Statistical Programming jobs in Cambridge, MA?

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What job categories do people searching Associate Director Statistical Programming jobs in Cambridge, MA look for?

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What cities near Cambridge, MA are hiring for Associate Director Statistical Programming jobs?

Cities near Cambridge, MA with the most Associate Director Statistical Programming job openings:

Infographic showing various Associate Director Statistical Programming job openings in Cambridge, MA as of August 2026, with employment types broken down into 100% Full Time. Highlights an 60% In-person, and 40% Hybrid job distribution, with an average salary of $306,194 per year, or $147.2 per hour.

Associate Director, Biostatistics

Clinical Dynamix, Inc.

Burlington, MA • On-site

Full-time

Re-posted 20 days ago


Job description

Associate Director, Biostatistics Job Description:

Position Summary

The Associate Director, Biostatistics is responsible for partnering with clinical, regulatory, data

management and statistical programming teams to deliver robust statistical methodologies that

advance clinical program objectives and ensure compliance with industry standards. This

individual will contribute to the success of the team and organization by delivering on role-

specific responsibilities while upholding our core working behaviors of Trust and Respect,

Communication and Feedback, Accountability and Reliability, Objectivity, and Team Balance and

Enablement.

Key Responsibilities

• Serve as the lead statistician for clinical trials, contributing to efficient study design and

rigorous data analysis.

• Provide high-quality statistical support across clinical programs, ensuring scientific

robustness and alignment with development goals.

• Design and refine clinical trial methodologies; author study synopses and protocols.

• Collaborate with data management on CRF design and database quality to ensure reliable

datasets.

• Develop statistical analysis plans and ensure clear, transparent documentation.

• Guide and mentor statistical programmers in creating SDTM/ADaM specifications, datasets,

and statistical outputs.

• Review and approve statistical deliverables to ensure consistency, accuracy, and regulatory

readiness.

• Interpret study results and contribute to clinical reports, presentations, publications, and

regulatory documentation.

• Author statistical content for regulatory submissions and support interactions with global

health authorities.

• Monitor timelines, deliverables, and support resource planning to keep programs on track.

• Participate in vendor selection and provide oversight to ensure high-quality, timely

statistical outputs.

• Contribute to the development and evolution of Biostatistics processes, standards, and best

practices at Company.

• Communicate proactively, collaborate effectively, and maintain a solutions-oriented

approach in a dynamic, fast-paced environment.

• Demonstrate ownership, accountability, and a commitment to delivering high-quality work.

• Provide constructive feedback to support team development and shared success.

Skills and Qualifications

• PhD in Biostatistics or related field with 5+ years of industry experience, or MS with 7+

years.

• Experience in oncology drug development preferred.

• Strong knowledge of FDA, EMA, and ICH guidelines, and a solid understanding of the end-to-

end drug development process.

• Expertise in statistical methods for clinical trials, up to date knowledge of statistical

applications and the ability to communicate complex concepts clearly to diverse audiences.

• Proficiency in SAS and R, and familiarity with CDISC SDTM and ADaM standards.

• Experience contributing to NDAs, MAAs, or other global regulatory submissions.

• Ability to collaborate effectively with CRO partners and manage outsourced statistical

activities.

• Strong interpersonal and communication skills, with the ability to build trust and guide

cross-functional decision-making.

• Demonstrated accountability, strong analytical thinking, and a data-driven approach to

problem-solving.

• Ability to work both independently and within a collaborative, matrixed team environment.

• Sense of urgency, initiative, and adaptability in a fast-moving, small-company setting.

• Excellent organizational, time management, and project leadership skills.

• High attention to detail and strong problem-solving capabilities.

• Willingness to learn, grow, and contribute to Company’s mission.

Working Behaviors (Core Expectations)

• Trust and Respect: Act with integrity, honesty, and openness to build strong, credible

relationships.

• Communication and Feedback: Share information clearly, listen actively, and engage in a

culture of constructive feedback.

• Accountability and Reliability: Take ownership for performance, be dependable, and support

others to achieve collective goals.

• Objectivity: Align on common objectives and use facts and data to reach fair, effective

decisions.

• Team Balance and Enablement: Contribute to balanced roles within the team, support

delegation, and help colleagues reach their full potential.