Green Card Senior Statistical Programmer Jobs
Senior Statistical Programmer roles at U.S. biotech, pharmaceutical, and CRO employers frequently qualify for EB-2 or EB-3 green card sponsorship through PERM labor certification. Your advanced degree in statistics, biostatistics, or a related field, combined with SAS or R programming expertise, positions you strongly for employment-based permanent residency.
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Get Access To All JobsINTRODUCTION
About Certara
Certara accelerates the potential of bringing medicines to market and to patients using biosimulation software, technology, and services to transform traditional drug discovery and development. Our clients include more than 2,400 biopharmaceutical companies, academic institutions, and regulatory agencies across 70 countries.
Our goal is to enable the life sciences industry’s use of data, modeling, and analytics to make better decisions across the various phases of discovery and drug development. Our software and scientists incorporate modern advances in scientific understanding, drug development experience, data analysis, and AI resulting in significant opportunities to decrease the cost and increase the probability of success for new drug approval and commercialization.
Responsibilities
As a Statistical Programming Consultant, you will use your SAS and R programming skills to prepare SDTM and ADaM datasets, Tables, Listings, & Figures (TLFs), as well as create related documents such as aCRF, programming specifications, and define packages (including reviewer’s guides) for Phase 1 to Phase 4 clinical trials. Advanced SAS macro programming experience is required for the development of global tools that will increase the efficiency and capacity of the Statistical Programming group. Preclinical SEND dataset preparation is a plus. Experience with NDA/IND-type regulatory submissions is preferred.
In addition, you will conduct quality control and quality assurance activities on datasets and outputs and may participate in company initiatives to improve the efficiency of end-to-end statistical programming activities, analysis, and reporting (IT, methodology, automation, quality). You will work closely in teams led by statistical programmers, statisticians, and drug development consultants, supporting a variety of client projects across various therapeutic areas and complexities.
BASIC QUALIFICATIONS
- B.Sc., M.Sc., or equivalent education in Biostatistics/Statistics, Bioinformatics, Life Sciences, Mathematics, Physical Sciences, or related fields.
- At least 6 years of Clinical trials related work experience in SAS programming, analysis and reporting in the context of drug development projects is required.
- Well experienced in the Pinnacle 21 validation process, generating Define.xml using Pinnacle 21.
- Extensive experience in implementing CDISC standards, as well as annotating CRFs, creating specifications for SDTM and ADaM datasets.
- Experienced in creating Define.xml and the corresponding Reviewers’ Guide for SDTM and ADaM datasets.
- Good verbal and written communications skills in English.
- Demonstrated knowledge of clinical drug development.
- Proficiency in conducting advanced statistical analyses.
- Must be independent, attention to detail, accountable to quality and timely delivery.
- Ability to work on multiple collaborative projects, team player mentality.
- Experience with the R software platform (in addition to SAS) is a plus.
Certara bases all employment-related decision on merit, taking into consideration qualifications, skills, achievement, and performance. We treat all applicants and employees without regard to personal characteristics such as race, color, ethnicity, religion, sex, sexual orientation, age, nationality, marital status, pregnancy, physical or mental condition, genetic information, military service, or other characteristic protected by law.
INTRODUCTION
About Certara
Certara accelerates the potential of bringing medicines to market and to patients using biosimulation software, technology, and services to transform traditional drug discovery and development. Our clients include more than 2,400 biopharmaceutical companies, academic institutions, and regulatory agencies across 70 countries.
Our goal is to enable the life sciences industry’s use of data, modeling, and analytics to make better decisions across the various phases of discovery and drug development. Our software and scientists incorporate modern advances in scientific understanding, drug development experience, data analysis, and AI resulting in significant opportunities to decrease the cost and increase the probability of success for new drug approval and commercialization.
Responsibilities
As a Statistical Programming Consultant, you will use your SAS and R programming skills to prepare SDTM and ADaM datasets, Tables, Listings, & Figures (TLFs), as well as create related documents such as aCRF, programming specifications, and define packages (including reviewer’s guides) for Phase 1 to Phase 4 clinical trials. Advanced SAS macro programming experience is required for the development of global tools that will increase the efficiency and capacity of the Statistical Programming group. Preclinical SEND dataset preparation is a plus. Experience with NDA/IND-type regulatory submissions is preferred.
In addition, you will conduct quality control and quality assurance activities on datasets and outputs and may participate in company initiatives to improve the efficiency of end-to-end statistical programming activities, analysis, and reporting (IT, methodology, automation, quality). You will work closely in teams led by statistical programmers, statisticians, and drug development consultants, supporting a variety of client projects across various therapeutic areas and complexities.
BASIC QUALIFICATIONS
- B.Sc., M.Sc., or equivalent education in Biostatistics/Statistics, Bioinformatics, Life Sciences, Mathematics, Physical Sciences, or related fields.
- At least 6 years of Clinical trials related work experience in SAS programming, analysis and reporting in the context of drug development projects is required.
- Well experienced in the Pinnacle 21 validation process, generating Define.xml using Pinnacle 21.
- Extensive experience in implementing CDISC standards, as well as annotating CRFs, creating specifications for SDTM and ADaM datasets.
- Experienced in creating Define.xml and the corresponding Reviewers’ Guide for SDTM and ADaM datasets.
- Good verbal and written communications skills in English.
- Demonstrated knowledge of clinical drug development.
- Proficiency in conducting advanced statistical analyses.
- Must be independent, attention to detail, accountable to quality and timely delivery.
- Ability to work on multiple collaborative projects, team player mentality.
- Experience with the R software platform (in addition to SAS) is a plus.
Certara bases all employment-related decision on merit, taking into consideration qualifications, skills, achievement, and performance. We treat all applicants and employees without regard to personal characteristics such as race, color, ethnicity, religion, sex, sexual orientation, age, nationality, marital status, pregnancy, physical or mental condition, genetic information, military service, or other characteristic protected by law.
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Get Access To All JobsTips for Finding Green Card Sponsorship in Senior Statistical Programmer
Verify your degree maps to EB-2
EB-2 requires an advanced degree directly related to the role. A master's or PhD in biostatistics, statistics, or epidemiology typically satisfies this. A bachelor's plus five years of progressive clinical-trial programming experience can substitute under DOL guidelines.
Document SAS validation work before applying
PERM audits for statistical programmer roles often scrutinize specialty occupation evidence. Compile validation summaries, CDISC SDTM and ADaM dataset deliverables, and any FDA submission contributions now, before your employer files the labor certification.
Target CROs and pharma sponsors with PERM history
Contract research organizations and mid-to-large pharmaceutical companies routinely sponsor foreign statistical programmers through PERM. Search OFLC Wage Search to identify employers who have certified LCAs for Senior Statistical Programmer titles in your target location.
Search Migrate Mate to find sponsoring employers fast
Filter by green card sponsorship history and job title to surface employers actively hiring Senior Statistical Programmers. Migrate Mate surfaces PERM and LCA filing data so you can prioritize outreach to companies with a documented track record of sponsoring this role.
Confirm the prevailing wage level before accepting an offer
Your employer must pay at least the DOL prevailing wage for your location and experience tier. Use OFLC Wage Search to look up the Level III or Level IV wage for the O*NET occupation code covering senior statistical programming before you negotiate.
Understand the PERM timeline so you can plan status continuity
PERM labor certification currently takes 12 to 18 months with DOL, followed by I-140 adjudication with USCIS. If you're on H-1B visa, your employer should file PERM well before your sixth year to preserve extension eligibility under AC21 portability rules.
Green Card Senior Statistical Programmer: Frequently Asked Questions
Do Senior Statistical Programmer roles qualify for EB-2 or EB-3 green card sponsorship?
Most do, and many qualify for both categories. EB-2 applies when the position requires a master's degree or higher in statistics, biostatistics, or a closely related field. EB-3 covers roles requiring a bachelor's degree plus relevant experience. Your employer chooses the category based on the actual job requirements, not your personal credentials, so the posted minimum qualifications matter.
How does PERM green card sponsorship differ from H-1B sponsorship for this role?
H-1B is a temporary work visa capped at 65,000 slots annually, requiring a lottery for most applicants. PERM-based green card sponsorship has no annual visa cap at the EB-3 level for most countries, and it leads to permanent residency rather than a renewable temporary status. The tradeoff is timeline: PERM plus I-140 plus adjustment of status typically runs three to five years, while H-1B approval can take a few months.
How can I find employers who have sponsored Senior Statistical Programmers before?
Use Migrate Mate to filter job listings by green card sponsorship history and job title. The platform surfaces PERM and LCA filing records so you can identify CROs, pharmaceutical companies, and biotech firms that have a documented track record of sponsoring this specific role, which reduces the risk of pursuing employers who are unfamiliar with the PERM process.
What documentation should I prepare to support a PERM filing as a statistical programmer?
Compile degree transcripts, SAS or R certification records, and work samples demonstrating CDISC-compliant SDTM and ADaM programming, FDA submission contributions, and validation deliverables. DOL audits for specialty occupation roles frequently request evidence that the position genuinely requires an advanced degree, so your employer's attorney will need detailed job duty documentation alongside your credentials.
Can I switch employers during the green card process without losing my place?
Yes, in many cases. Under AC21 portability rules, if your I-140 has been approved and your I-485 has been pending for at least 180 days, you can move to a same or similar occupation without restarting the process. Senior Statistical Programmer roles at different sponsors generally satisfy the same-or-similar standard, but USCIS reviews each case individually, so consult your immigration attorney before making any move.