FREE ACCESS
5,000–10,000 jobs/day

See all jobs on JobTailor
Search thousands of fresh jobs every day.
Discover
- Fresh listings
- Fast filters
- No subscription required
Create a free account and start exploring right away.

Senior Manager, Statistical Programming
BioNTech SESenior Manager, Statistical Programming overseeing high-quality statistical programming deliverables at BioNTech. Collaborating with Clinical Development teams and CROs to support clinical projects and regulatory submissions.
Posted 4/23/2026full-timeCambridge • Maryland, Massachusetts, New Jersey • 🇺🇸 United StatesSenior💰 $130,800 - $198,200 per yearWebsite
Tech Stack
Tools & technologiesSQL
About the role
Key responsibilities & impact- Collaborate with Clinical Development teams or CROs to meet project timelines for statistical data analysis and reporting
- Oversee or independently produce and validate programming deliverables such as analysis datasets, tables, listings, and figures
- Anticipate resource needs and coordinate with management to ensure long-term resource allocation for therapeutic projects
- Ensure quality control (QC) is performed on all derived datasets, tables, listings, and figures in alignment with company standards and regulatory requirements
- Participate in developing global programming standards to enable consistent deliverables across portfolios; create tools supporting SDTM/ADaM dataset generation and TLF production
- Provide functional expertise in establishing BioNTech’s centralized clinical data repository, clinical data dictionary, and operational data dictionary
- Collaborate with Biostatistics to develop statistical applications such as data review and reporting tools
- Support regulatory submissions by preparing data submission packages including define.xml
Requirements
What you’ll need- BSc in Statistics, Mathematics, Computer Science, or related discipline; advanced degree preferred
- 5+ years (3+ years with advanced degree) experience in pharmaceutical industry/CRO/clinical research settings
- Strong competence in statistical programming (e.g., SAS/Base, Macro, STAT, GRAPH, SQL)
- Solid knowledge of FDA/EMA/ICH regulations and guidelines governing clinical trials
- Familiarity with industry standards for clinical study data reporting (e.g., CDISC standards)
- Experience in oncology therapeutic area; submission experience preferred
- Project management skills with strong organizational abilities and attention to detail
- Excellent communication skills (written/spoken English) with a proactive mindset for problem-solving
- Ability to thrive in a fast-paced team environment while maintaining analytical rigor
Benefits
Comp & perks- Medical, Dental and Vision Insurance
- Life, AD&D, Critical Illness Insurance
- Pre-tax HSA & FSA, DCRA Spending Accounts
- Employee Assistance & Concierge Program (EAP) available 24/7
- Parental and Childbirth Leave & Family Planning Assistance
- Sitterstream: Virtual Tutoring & Childcare Membership
- Paid Time Off: Vacation, Sick, Bereavement, Holidays (including Floating) & Year-End U.S. Shutdown
- 401(K) Plan with Company Match
- Tuition Reimbursement & Student Loan Assistance Programs
- Wellbeing Incentive Platforms & Incentives
- Professional Development Programs
- Commuting Allowance and subsidized parking
- Discounted Home, Auto & Pet Insurance
- …and more!
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
statistical programmingSASSQLdata analysisdata validationdataset generationTLF productionprogramming deliverablesdefine.xml preparationstatistical applications
Soft Skills
project managementorganizational abilitiesattention to detailcommunication skillsproblem-solvingcollaborationproactive mindsetanalytical rigorresource coordinationquality control