Senior Manager, Statistical Programming
Ascendis Pharma
Posted: 10/20/2026Python
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Senior Manager, Statistical Programming
Ascendis PharmaPosted 10/20/2026full-timePalo Alto • California • United StatesSenior💰 $170,000 - $180,000 per yearWebsite
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in Statistical Programming for clinical trials, with a strong focus on CDISC standards, SAS programming, and project management. Capable of leading programming efforts while ensuring compliance with regulatory requirements and quality expectations.
Highest-signal resume keywords
Statistical Programming LeadSAS ProgrammingCDISC StandardsSDTM and ADaM DatasetsClinical Trials Experience
Tech Stack
Tools & technologiesAbout the role
Key responsibilities & impact- Provide timely and strategic programming support to clinical study teams in alignment with project goals
- Serve as Statistical Programming Lead for one or more clinical trials
- Oversee all programming deliverables from study start through regulatory submission
- Represent Statistical Programming in cross-functional study team meetings
- Contribute to project planning and timelines
- Develop, validate, and maintain SDTM and ADaM datasets according to CDISC standards and study specifications
- Generate or validate tables, listings, and figures (TLFs) for clinical study reports, ISS/ISE, and regulatory submissions
- Support statisticians with planned and ad hoc analyses
- Develop and maintain reusable macros, templates, and specification tools
- Collaborate with Biostatistics, Data Management, and Medical Writing
- Ensure programming activities meet project timelines and quality expectations under internal SOPs and industry best practices
Requirements
What you’ll need- Bachelor’s degree in Statistics, Mathematics, Computer Science, or related field with at least 10 years of programming experience in the pharmaceutical or biotech industry; or a Master’s degree with at least 7 years of relevant experience
- Proven experience as a lead programmer for clinical trials and complex technical projects
- Excellent knowledge of CDISC standards, including SDTM and ADaM
- Understanding of the clinical drug development process and regulatory requirements
- Proficiency in SAS programming, including the ability to develop and validate reusable macros
- Familiarity with R, Python, Git, or VB is a plus
- Experience contributing to departmental tools such as macro libraries, specification templates, or automation tools is preferred
- Strong verbal and written communication skills, with the ability to collaborate effectively across functions
- Self-motivated and detail-oriented, with the ability to manage multiple tasks and adapt to shifting priorities under tight deadlines
Benefits
Comp & perks- 401(k) plan with company match
- Medical, dental, and vision plans
- Company-offered Life and Accidental Death & Dismemberment (AD&D) insurance
- Company-provided short and long-term disability benefits
- Unique offerings of Pet Insurance and Legal Insurance
- Employee Assistance Program
- Employee Discounts
- Professional Development
- Health Saving Account (HSA)
- Flexible Spending Accounts
- Various incentive compensation plans
- Accident, Critical Illness, and Hospital Indemnity Insurance
- Mental Health resources
- Paid leave benefits for new parents
- Discretionary annual bonus or incentive compensation plan eligibility
- Discretionary stock-based long-term incentives
- Paid time off
- Comprehensive benefits package
- Flexible/remote work option
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Statistical ProgrammingSAS ProgrammingCDISC StandardsSDTMADaMData ValidationMacro DevelopmentStatistical AnalysisRegulatory SubmissionProject Planning
Soft Skills
Strong Communication SkillsDetail-OrientedSelf-MotivatedCollaborationAdaptability
Tools & Technologies
RPythonGitVBMacro LibrariesSpecification TemplatesAutomation Tools
Industry Keywords
Pharmaceutical IndustryBiotech IndustryClinical Drug DevelopmentRegulatory RequirementsCross-Functional Collaboration