Apply

Ready to go for it?

AI Apply speeds things up—apply directly if you prefer.

FREE ACCESS
5,000–10,000 jobs/day
JobTailor Logo

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.
BioNTech SE

Senior Manager, Statistical Programming

BioNTech SE

Senior 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 & technologies
SQL

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 resume
Applicant 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