Senior Statistical Programmer Green Card 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 JobsAre you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it’s the best of both worlds…. ClinChoice is searching for a Senior Statistical Programmer Consultant to join one of our clients. ClinChoice is a global full-service CRO with a strong focus on quality, professional development, and supportive culture. As a client-facing role, we are looking for confident candidates with the ability to work independently whilst establishing a high-trust environment with the client’s counterparts.
Location: NJ/PA/DE; Hybrid role in any of these location
Job Summary
The contract Senior Statistical Programmer is a member of the Biometrics Department within the Research and Development (R&D) organization who supports Statistical programming work in accordance with corporate standard operating procedures (SOPs), GCP, 21 CFR and ICH guidance.
Responsibilities
Programing for clinical trials:
- Program and validate derived datasets, tables, figures, listings.
- Process data from the external sources.
- Perform ad hoc exploratory analyses for publications and programming support other functions of Research and Development or other organizations.
- Oversee programing work/deliverables from CROs.
- Contribute to the design/implementation/review of Case Report Form, Data Transfer Specification, Statistical Analysis Plan, SDTM/ADaM Specification documents, Define packages.
Electronic submissions:
- Program and validate CDISC compliant deliveries for the electronic submissions.
- Support in the creation of supporting documentation for submissions.
Project Management:
- Ensure programming deliverables are on time and of high quality.
- Help managing internal contractors and external vendors.
Standards and Guidelines:
- Participate in development of departmental working instructions and guidelines.
- Help in creation of enhanced functions/macros and utilities.
Qualification & Experience
- Bachelor or Master degree in Computer Science, Mathematics, Engineering, Medical or related discipline.
- BS with more than 5 or MS with 3 years of experience in statistical programming (SAS, R) in the pharmaceutical industry.
- Working knowledge of SAS and its various components.
- Knowledge of R programming in clinical trials
- Familiarity of the drug development process.
- Strong SAS and SAS Macro language skills.
- R programming skills in clinical trials
- Strong knowledge of industry standards.
- Ability to work on data integrations (ISS and ISE).
- Strong oral and written communication skills. Ability to communicate details of the analysis to other team members with less technical experience.
The Application Process
Once you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for phone interview as the first step. Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.
Who will you be working for?
About ClinChoice
ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of proven high-quality delivery and results across all our services, with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific.
Our Company Ethos
Our mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Our employees are the most valuable company asset and they are the fulcrum around which all ClinChoice activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives all personnel the clear tools needed to manage both internal and client processes with the same methodology. The success of these core values is evidenced by our below industry average turnover rates. ClinChoice is an equal opportunity employer. We have based our success on attracting, developing, and promoting talent guided by diversity and inclusivity. Our employees come from very diverse backgrounds: gender, race, beliefs, and ethnicities. We recognize this is our strength and celebrate it.
#senior#contract
Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it’s the best of both worlds…. ClinChoice is searching for a Senior Statistical Programmer Consultant to join one of our clients. ClinChoice is a global full-service CRO with a strong focus on quality, professional development, and supportive culture. As a client-facing role, we are looking for confident candidates with the ability to work independently whilst establishing a high-trust environment with the client’s counterparts.
Location: NJ/PA/DE; Hybrid role in any of these location
Job Summary
The contract Senior Statistical Programmer is a member of the Biometrics Department within the Research and Development (R&D) organization who supports Statistical programming work in accordance with corporate standard operating procedures (SOPs), GCP, 21 CFR and ICH guidance.
Responsibilities
Programing for clinical trials:
- Program and validate derived datasets, tables, figures, listings.
- Process data from the external sources.
- Perform ad hoc exploratory analyses for publications and programming support other functions of Research and Development or other organizations.
- Oversee programing work/deliverables from CROs.
- Contribute to the design/implementation/review of Case Report Form, Data Transfer Specification, Statistical Analysis Plan, SDTM/ADaM Specification documents, Define packages.
Electronic submissions:
- Program and validate CDISC compliant deliveries for the electronic submissions.
- Support in the creation of supporting documentation for submissions.
Project Management:
- Ensure programming deliverables are on time and of high quality.
- Help managing internal contractors and external vendors.
Standards and Guidelines:
- Participate in development of departmental working instructions and guidelines.
- Help in creation of enhanced functions/macros and utilities.
Qualification & Experience
- Bachelor or Master degree in Computer Science, Mathematics, Engineering, Medical or related discipline.
- BS with more than 5 or MS with 3 years of experience in statistical programming (SAS, R) in the pharmaceutical industry.
- Working knowledge of SAS and its various components.
- Knowledge of R programming in clinical trials
- Familiarity of the drug development process.
- Strong SAS and SAS Macro language skills.
- R programming skills in clinical trials
- Strong knowledge of industry standards.
- Ability to work on data integrations (ISS and ISE).
- Strong oral and written communication skills. Ability to communicate details of the analysis to other team members with less technical experience.
The Application Process
Once you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for phone interview as the first step. Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.
Who will you be working for?
About ClinChoice
ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of proven high-quality delivery and results across all our services, with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific.
Our Company Ethos
Our mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Our employees are the most valuable company asset and they are the fulcrum around which all ClinChoice activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives all personnel the clear tools needed to manage both internal and client processes with the same methodology. The success of these core values is evidenced by our below industry average turnover rates. ClinChoice is an equal opportunity employer. We have based our success on attracting, developing, and promoting talent guided by diversity and inclusivity. Our employees come from very diverse backgrounds: gender, race, beliefs, and ethnicities. We recognize this is our strength and celebrate it.
#senior#contract
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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, your employer should file PERM well before your sixth year to preserve extension eligibility under AC21 portability rules.
Senior Statistical Programmer jobs are hiring across the US. Find yours.
Find Senior Statistical Programmer JobsSenior Statistical Programmer Green Card Sponsorship: 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.
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