ZipRecruiter

Log In

1

Associate Director Statistical Programming Jobs in Boston, MA

Takeda

Associate Director, Statistics

Boston, MA · Hybrid

$64K - $64K/yr

... Programming, Patient Safety & Pharmacovigilance, and Strategic Operations The Statistics and ... It leverages cutting-edge technology, machine learning, AI, and statistical methods to analyze ...

Takeda

Associate Director, Statistics

Boston, MA · Hybrid

$64K - $64K/yr

... Programming, Patient Safety & Pharmacovigilance, and Strategic Operations The Statistics and ... It leverages cutting-edge technology, machine learning, AI, and statistical methods to analyze ...

next page

Showing results 1-20

All JobsAssociate Director Statistical Programming JobsAssociate Director Statistical Programming Jobs in Boston, MA

Associate Director Statistical Programming information

See Boston, MA salary details

$166.8K

$304.3K

$373.7K

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

As of Jun 9, 2026, the average yearly pay for associate director statistical programming in Boston, MA is $304,336.00, according to ZipRecruiter salary data. Most workers in this role earn between $283,000.00 and $350,300.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as an Associate Director Statistical Programming, and why are they important?

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.

What does an Associate Director of 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.

How does an Associate Director of 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 Boston, MA? For Associate Director Statistical Programming jobs in Boston, MA, the most frequently searched job titles are:
What job categories do people searching Associate Director Statistical Programming jobs in Boston, MA look for? The top searched job categories for Associate Director Statistical Programming jobs in Boston, MA are:
What cities near Boston, MA are hiring for Associate Director Statistical Programming jobs? Cities near Boston, MA with the most Associate Director Statistical Programming job openings:
Associate Director Statistical Programming jobs near you
Infographic showing various Associate Director Statistical Programming job openings in Boston, MA as of June 2026, with employment types broken down into 100% Full Time. Highlights an 91% In-person, and 9% Remote job distribution, with an average salary of $304,336 per year, or $146.3 per hour.
Associate Director / Director, Data Management

Associate Director / Director, Data Management

Beam Therapeutics

Cambridge, MA • On-site

Full-time

Posted 18 days ago

Job description

Company Overview:
Beam Therapeutics is a biotechnology company committed to establishing the leading, fully integrated platform for precision genetic medicines. To achieve this vision, Beam has assembled a platform with integrated gene editing, delivery and internal manufacturing capabilities. Beam's suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA. This has the potential to enable a wide range of therapeutic editing strategies that Beam is using to advance a diversified portfolio of base editing programs. Beam is a values-driven organization committed to its people, cutting-edge science, and a vision of providing life-long cures to patients suffering from serious diseases.
Position Overview:
Reporting to the Senior Director, Clinical Data Management, the Associate Director / Director, Clinical Data Management will serve as the dedicated data management lead for our Liver franchise. Initially supporting a single study within the program, this individual will grow with the franchise as it expands to include additional studies within the same program and, ultimately, other programs across the franchise portfolio.
This role offers a unique blend of hands-on study oversight and strategic leadership, making it an ideal opportunity for a candidate who thrives at the intersection of execution and innovation, in a fast-paced biotech environment where clarity, quality, and collaboration are critical.
This is a highly visible role working cross-functionally with Clinical Development, Biostatistics, Statistical Programming, Regulatory, Quality, and external partners to ensure data integrity, inspection readiness, and timely delivery of data supporting key development and regulatory milestones.
Primary Responsibilities:
Program & Study Ownership
  • Lead sponsor side clinical data management activities across multiple concurrent studies within a defined therapeutic area.
  • Own data management execution from study start-up through database lock and archival for concurrent studies, including late stage and registrational trials.
  • Ensure data quality, integrity, and traceability to support interim analyses, CSRs, DSURs, IB updates, and program specific regulatory interactions.
  • Proactively identify data risks, trends, and operational dependencies; communicate issues early with clear, solution-oriented recommendations.

CRO & Vendor Oversight
  • Serve as the primary data management contact for CROs and third-party data vendors.
  • Oversee outsourced CDM activities to ensure timely, high-quality deliverables aligned with sponsor' expectations.
  • Monitor CRO and vendor performance, escalating risks and proposing mitigation strategies in partnership with the Senior Director of Data Management.

Data Standards, Systems & Process Contribution
  • Contribute expert input to the development and evolution of data management standards, processes, tools/systems and vendor operating models as the organization scales its clinical portfolio.
  • Provide hands-on leadership for:
    • CRF design and cross functional review
    • Edit check specifications and user acceptance testing
    • Data Management Plans and CRF Completion Guidelines
    • External data transfer specifications
  • Apply CDASH/CDISC expertise and partner with Statistical Programming to support SDTM readiness, validation outputs, Reviewer's Guides, and define.xml.

Inspection Readiness
  • Support inspection readiness activities across assigned programs, ensuring documentation and data traceability meet regulatory expectations.
  • Serve as a key data management participant during audits and inspections, in coordination with the Senior Director and Quality.
  • Ensure data management deliverables remain inspection ready throughout the study lifecycle.

Cross-Functional Partnership
  • Collaborate closely with Clinical Operations, Biostatistics, Statistical Programming, Medical Monitoring, Regulatory, and Quality.
  • Communicate complex data issues clearly and effectively to stakeholders with varying technical backgrounds.
  • Build trust as a pragmatic, detail-oriented partner who balances scientific rigor with efficient execution.

Required Qualifications:
  • BS or MS degree in a scientific or health-related field.
  • 10+ years of experience in clinical data management within pharmaceutical/biotech and/or CRO environments.
  • Demonstrated sponsor-side ownership of Phase I, II and III studies, from start-up through closure for multiple clinical studies.
  • Strong hands-on experience with EDC systems (e.g., Medidata RAVE, Veeva EDC, Oracle Inform).
  • Deep knowledge of CDASH/CDISC, GCP/ICH, and FDA regulatory expectations.
  • Proven experience overseeing CROs and external data vendors.
  • Experience developing reports using J-Review and/or other CDM reporting tools.
  • Prior IND, as well as NDA/BLA (filing/submission) experience, is highly desirable.
  • Must be self-motivating, with strong analytical, organizational, and communication skills, with the ability to manage complexity across multiple studies.
  • Demonstrated ability to navigate evolving priorities and drive timelines forward with focus and composure in a fast-moving organization.

Preferred Qualifications:
  • Experience and knowledge of gene/cell therapy and/or rare disease.
  • Prior experience supporting registrational or pre registrational programs.

The salary range below reflects the full-time base salary range we expect to pay for this role at the time of posting. Base pay will be determined based on several factors including, but not limited to, relevant experience, education, scope of job, internal comparisons, and market data.
Beam Pay Range
$185,000-$260,000 USD

Apply