Vor Bio · 1 month ago
Associate Director, Statistical Programing
Boston
Full-time
Onsite
Lead/Staff, Director/Executive
$205K/yr - $230K/yr
8+ years expVor BioPharma is focused on redefining the future of autoimmune care by advancing innovative therapies. The Associate Director, Statistical Programming will lead statistical analysis efforts in clinical studies, collaborating with various teams to ensure quality and compliance in data processing and reporting.
BiotechnologyHealth CareOncologyPharmaceutical
Responsibilities
Serve as a Lead study programmer to support activities including review SAP, set up mock TFL, dry run, draft and final TFLs
Collaborate with other functions for the requirement i.e. Safety update, publications etc
Effectively design and develop SAS programs including micros for efficiency and consistency
May involve in the standardization and process improvement initiatives
Supporting FDA submission as needed
Codes complex SAS programs (including Macro language, SAS/STAT and SAS/GRAPH) for applications designed to analyze and report complex clinical trial data and for electronic review, exchange, transformation, and submission of data in CDISC SDTM format; consistently meeting objectives of the study
Performs quality control checks of SAS code and output produced by other Statistical Programmers
Demonstrates proficient knowledge of clinical development and medical data
Solves clinical trial reporting problems and has a proven technical proficiency in supporting daily operations and ensuring that project tasks are completed accurately with limited supervision
Creates CDISC data sets by transforming various raw data sources, including different Electronic Data Capture (EDC) databases and Interactive Web Response Systems (IWRS), tables, figures, and listings reporting and submitting the results of clinical trials for investigational medications
Works with all types of coding dictionaries (MedDRA and WHODD) commonly used by the pharmaceutical industry
Works in a team environment providing technical leadership and solving clinical trial reporting problems within budget and customary time line constraints while assuring high quality standards
Qualification
Required
A Master degree in Statistics, Mathematics, computer science or other equivalents
Minimum 8 years of SAS programming in a pharmaceutical, biotech or CRO setting
Strong knowledge in CDISC including SDTM, ADaM, metadata, controlled terminologies, and data flows, as well as in industry standards for electronic submission of data to FDA
Strong hands-on SAS programming skills and working experience for clinical trial reporting
Ability to handle multiple development programs simultaneously
Ability to be flexible and adapt quickly to the changing needs of the organization
Strong interpersonal and effective communication (oral and written) skills
Benefits
Comprehensive health coverage
Flexible paid time off
Generous parental leave
Competitive 401(k)
Education assistance
Wellness resources
Financial security
Company
Vor Bio
Vor Bio is a clinical-stage biotechnology company transforming the treatment of autoimmune diseases.
2-10 employees
H1B Sponsorship
Vor Bio has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (6)
2024 (5)
2023 (6)
2022 (10)
2021 (1)
2020 (1)
Funding
Current Stage
Public CompanyTotal Funding
$748.4MKey Investors
RA Capital Management
2025-12-15Post Ipo Equity· $150M
2025-11-10Post Ipo Equity· $100M
2025-06-24Post Ipo Equity· $175M
Leadership Team
Jean-Paul Kress
Chairman and CEO
Dallan Murray
EVP, Chief Commercial Officer
Recent News
GlobeNewswire
2025-12-15
2025-12-15
Company data provided by crunchbase