Top 181 Director statistical programming Jobs

Director, Statistical Programming
Seaport Therapeutics —Boston, MA
- $198,000 - $233,000 a year
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- Bachelor of Science
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Alexion Pharmaceuticals,Inc. —Wilmington, DE
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Baptist Memorial Health —Memphis, TN
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Associate Director, Statistics
Takeda Pharmaceutical —Boston, MA
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Northrop Grumman —El Segundo, CA
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Director, Statistical Programming
CSL Behring —Waltham, MA
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Associate Director, Statistical Programming
Corcept Therapeutics —Redwood City, CA
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Associate Director, Statistical Programming
Alkermes, Inc. —Waltham, MA
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Avalo Therapeutics —Chesterbrook, PA
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Assoc Director, Statistical Programming
Gilead Sciences —Raleigh, NC
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Director, Statistical Programming
Puma Biotechnology —Los Angeles, CA
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Executive Director, Statistical Programming
Travere Therapeutics —San Diego, CA
- $246,000 - $332,000 a year
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Director, Statistical Programming
Kura Oncology —San Diego, CA
- $234,644 - $263,000 a year
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Associate Director/Senior Manager, Data Science (Statistical Programming)
Alumis —South San Francisco, CA
- $180,000 - $220,000 a year
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Associate Director, Statistical Programming
Servier —Boston, MA
- $165,000 - $200,000 a year
- Full-time
- 8 years
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5d

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Director, Statistical Programming

Seaport Therapeutics
Boston, MA

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Job Details

$198,000 - $233,000 a year

Qualifications

Procedural guides
SAS
FDA 21 CFR Part 11
SAS language
ICH guidelines
Pharmaceutical company experience
CDISC standards
Clinical trial standard operating procedures
Regulatory submission editing and review
Clinical quality assurance standards
Project stakeholder communication

Full Job Description

Seaport Therapeutics is a clinical-stage therapeutics company advancing the development of novel neuropsychiatric medicines in areas of high unmet patient needs. The Company has a proven strategy of advancing clinically validated mechanisms previously held back by limitations that are overcome with its proprietary GlyphTM technology platform. All the therapeutic candidates in its pipeline of first and best-in-class medicines are based on the Glyph platform, which is uniquely designed to enable oral bioavailability, bypass first-pass metabolism and reduce hepatotoxicity and other side effects. Seaport is led by an experienced team that invented and advanced important neuropsychiatric medicines and are guided by an extensive network of renowned scientists, clinicians and key opinion leaders. For more information, please visit www.seaporttx.com.

Seaport Therapeutics is hiring our first in-house Statistical Programming leader to build and lead the Statistical Programming function within the Biometrics department. Reporting to the VP, Head of Biometrics, this Director will provide strategic oversight of CRO/vendor programming activities, perform hands-on programming in SAS and R, and ensure high-quality, submission-ready deliverables that meet CDISC and global regulatory standards. In the near term, the role will focus on vendor governance, thorough review/QC of datasets and TLFs, and support for regulatory interactions, publications, and ongoing medical/safety monitoring. Longer term, this leader will establish processes and SOPs, recruit and develop a high-performing team, and serve as a key member of the Biometrics leadership team driving continuous improvement.

The ideal candidate will embrace a collaborative, innovative culture that embodies our values of service to patients impacted by mental health conditions, with a “we own it” mentality, demonstrating entrepreneurial spirit and technical excellence while fostering teamwork and continuous improvement. This position is based in Boston’s Seaport area, with a strong preference for being onsite 4 days per week.

Key Responsibilities:

Lead the Statistical Programming function for Seaport Therapeutics; serve as programming representative on study and program teams and within the Biometrics leadership group.
Provide strategic oversight and day-to-day governance of CROs and external programmers, including scope planning, timelines, quality metrics, and issue escalation.
Perform hands-on programming in SAS or R to review/QC vendor deliverables, develop analysis datasets (SDTM/ADaM), and generate tables, listings, and figures (TLFs).
Ensure compliance with CDISC standards (SDTM, ADaM), FDA/EMA/ICH guidance, and submission requirements (e.g., define.xml, reviewer’s guides, eCTD packages).
Support regulatory interactions (IND, NDA/BLA/MAA), including ad hoc analyses, briefing package outputs, and responses to information requests.
Partner with Biostatistics, Data Management, Clinical, and Safety to enable medical and safety monitoring, signal detection, and data-driven decision-making across ongoing trials.
Establish and maintain programming processes, SOPs, work instructions, and reusable libraries/macros; champion automation, reproducibility, and audit readiness.
Recruit, manage, mentor, and develop a team of statistical programmers as the portfolio grows; manage contractors/FSPs and oversee performance and career development.
Drive continuous improvement across standards, tools, and infrastructure (SAS/R environments, version control, code review practices) in collaboration with IT and QA.
Plan and manage resources and budgets for programming activities; contribute to vendor selection, governance frameworks, and performance/quality measures for delivery quality and timeliness.
Represent Statistical Programming in inspections and audits; ensure documentation completeness and compliance with 21 CFR Part 11, GCP, data privacy, and company SOPs.

Qualifications:

Advanced degree (MS/PhD) in Statistics, Biostatistics, Computer Science, Mathematics, or related discipline; BS with strong relevant experience considered.
10+ years of statistical programming experience in biotech/pharma/CRO settings, with 5+ years of people management.
Expert hands-on proficiency in SAS (Base, Macro, STAT, GRAPH, SQL) and strong working knowledge of R; experience with Python is a plus.
Demonstrated experience overseeing CROs/vendors and validating programming deliverables to CDISC standards (SDTM, ADaM).
Proven contribution to global submissions (e.g., NDA/BLA/MAA), including submission-ready datasets, TLFs, define.xml, reviewer’s guides, and CSR appendices.
Strong understanding of clinical development processes, ICH/GCP, FDA/EMA guidelines, and 21 CFR Part 11 compliance.
Track record of building teams, establishing SOPs and standards, and implementing automation and best practices for efficiency and quality.
Excellent communication, collaboration, and leadership skills; ability to translate technical concepts for non-technical stakeholders.
Therapeutic area experience in CNS/neuropsychiatry is a plus; passion for Seaport’s patient-centric mission is essential.

At Seaport, we believe transparency and fairness are key to building a culture of trust, respect, and collaboration. We care deeply about the happiness of our team and strive to ensure our total rewards (monetary and non-monetary) program reflects the value each person brings. The expected salary range for this role is $198,000-233,000 with the final offer based on experience, market data, and internal equity. We encourage open conversations with our talent acquisition team about compensation early in the process to ensure alignment from the start.

Apply Now

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