Data Analytics Consultant Visa Sponsorship Jobs in Maryland
Data analytics consultant roles in Maryland draw from a dense cluster of federal agencies, defense contractors, and health tech firms spanning the Baltimore-Washington corridor. Employers like Booz Allen Hamilton, Leidos, SAIC, and Johns Hopkins Medicine regularly sponsor skilled international professionals. Demand is especially strong in Bethesda, Rockville, Columbia, and Baltimore.
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Get Access To All JobsINTRODUCTION
Precigen (Nasdaq: PGEN) is a commercial-stage biopharmaceutical company specializing in the advancement of innovative precision medicines to address difficult-to-treat diseases with high unmet patient need. Precigen is dedicated to advancing scientific breakthroughs from proof-of-concept through commercialization. With a strong commitment to innovation, Precigen is developing a robust pipeline of differentiated therapies utilizing the company’s AdenoVerse® and UltraCAR-T® therapeutic platforms across its core focus areas of immuno-oncology, autoimmune disorders, and infectious diseases.
Position Summary
The Associate Director, Clinical Data is the sponsor's data management lead for every company-sponsored study, across Clinical Development and Medical Affairs. Data management is outsourced to CROs and specialty vendors; this role sets standards, oversees vendor delivery and owns sponsor accountability for data quality from database design through lock. The role works hand in hand with study leads and the Biostatistician so data are fit for analysis, submission and publication.
DUTIES AND RESPONSIBILITIES:
- Lead sponsor review and approval of data management plans, eCRF design, edit check specifications, data review plans and data transfer agreements.
- Oversee EDC build and participate in user acceptance testing; approve go-live.
- Monitor CRO data management performance against KPIs: query aging, data entry timeliness, open discrepancies and cleaning status.
- Own database lock readiness: lock checklists, reconciliation sign-off and sponsor approval to lock.
- Oversee integration and reconciliation of external data (central lab, IRT, eCOA/ePRO, imaging, biomarker) and SAE reconciliation with Safety.
- Oversee medical coding (MedDRA, WHODrug) with Clinical Science and Medical review.
- Partner with study leads and Clinical Science on ongoing clinical data review, listings and trend detection as part of risk-based quality management.
- Drive consistent data standards across the portfolio (CDASH collection, CDISC SDTM oversight) and reusable eCRF and edit-check libraries.
- Define data collection for Phase 3b/4, registry and chart review studies: abstraction forms, data dictionaries, source data quality checks and transfer specifications, proportionate to study risk.
- Ensure data management TMF artifacts are complete and current; support audits and inspections on data handling and computerized system validation.
- Contribute to vendor selection for CROs, EDC and specialty data vendors.
- Other duties as assigned.
EDUCATION AND EXPERIENCE:
- Bachelor's degree in life sciences, health informatics, computer science or related field
- 10+ years in clinical data management, including sponsor-side vendor oversight.
- Hands-on experience with major EDC platforms (e.g. Medidata Rave, Veeva CDMS) and external data reconciliation.
- Working knowledge of CDISC (CDASH, SDTM), MedDRA/WHODrug coding, ICH E6(R3) and 21 CFR Part 11.
- Experience taking studies through database lock and supporting a regulatory submission; RWE or observational study experience valued.
DESIRED KEY COMPETENCIES:
- Self-organizer, highly motivated, and keen attention to detail.
- Excellent interpersonal, verbal, and written communication skills are essential in this collaborative work environment.
- Ability to understand and execute the company’s mission and values.
- Maintain a high degree of ethical standard and trustworthiness.
- Exhibits an open mindset when approaching challenges and conflict.
- Ability to think and adapt to a rapidly changing environment and demands.
- Strong time management and organizational skills.
- Ability to manage multiple projects in a fast-paced environment.
INTRODUCTION
Precigen (Nasdaq: PGEN) is a commercial-stage biopharmaceutical company specializing in the advancement of innovative precision medicines to address difficult-to-treat diseases with high unmet patient need. Precigen is dedicated to advancing scientific breakthroughs from proof-of-concept through commercialization. With a strong commitment to innovation, Precigen is developing a robust pipeline of differentiated therapies utilizing the company’s AdenoVerse® and UltraCAR-T® therapeutic platforms across its core focus areas of immuno-oncology, autoimmune disorders, and infectious diseases.
Position Summary
The Associate Director, Clinical Data is the sponsor's data management lead for every company-sponsored study, across Clinical Development and Medical Affairs. Data management is outsourced to CROs and specialty vendors; this role sets standards, oversees vendor delivery and owns sponsor accountability for data quality from database design through lock. The role works hand in hand with study leads and the Biostatistician so data are fit for analysis, submission and publication.
DUTIES AND RESPONSIBILITIES:
- Lead sponsor review and approval of data management plans, eCRF design, edit check specifications, data review plans and data transfer agreements.
- Oversee EDC build and participate in user acceptance testing; approve go-live.
- Monitor CRO data management performance against KPIs: query aging, data entry timeliness, open discrepancies and cleaning status.
- Own database lock readiness: lock checklists, reconciliation sign-off and sponsor approval to lock.
- Oversee integration and reconciliation of external data (central lab, IRT, eCOA/ePRO, imaging, biomarker) and SAE reconciliation with Safety.
- Oversee medical coding (MedDRA, WHODrug) with Clinical Science and Medical review.
- Partner with study leads and Clinical Science on ongoing clinical data review, listings and trend detection as part of risk-based quality management.
- Drive consistent data standards across the portfolio (CDASH collection, CDISC SDTM oversight) and reusable eCRF and edit-check libraries.
- Define data collection for Phase 3b/4, registry and chart review studies: abstraction forms, data dictionaries, source data quality checks and transfer specifications, proportionate to study risk.
- Ensure data management TMF artifacts are complete and current; support audits and inspections on data handling and computerized system validation.
- Contribute to vendor selection for CROs, EDC and specialty data vendors.
- Other duties as assigned.
EDUCATION AND EXPERIENCE:
- Bachelor's degree in life sciences, health informatics, computer science or related field
- 10+ years in clinical data management, including sponsor-side vendor oversight.
- Hands-on experience with major EDC platforms (e.g. Medidata Rave, Veeva CDMS) and external data reconciliation.
- Working knowledge of CDISC (CDASH, SDTM), MedDRA/WHODrug coding, ICH E6(R3) and 21 CFR Part 11.
- Experience taking studies through database lock and supporting a regulatory submission; RWE or observational study experience valued.
DESIRED KEY COMPETENCIES:
- Self-organizer, highly motivated, and keen attention to detail.
- Excellent interpersonal, verbal, and written communication skills are essential in this collaborative work environment.
- Ability to understand and execute the company’s mission and values.
- Maintain a high degree of ethical standard and trustworthiness.
- Exhibits an open mindset when approaching challenges and conflict.
- Ability to think and adapt to a rapidly changing environment and demands.
- Strong time management and organizational skills.
- Ability to manage multiple projects in a fast-paced environment.
Data Analytics Consultant Job Roles in Maryland
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Search Data Analytics Consultant Jobs in MarylandData Analytics Consultant Jobs in Maryland: Frequently Asked Questions
Which companies in Maryland sponsor visas for data analytics consultants?
Maryland's federal contracting hub produces consistent sponsorship activity for data analytics consultants. Booz Allen Hamilton, Leidos, SAIC, Deloitte, and Accenture Federal Services all have documented sponsorship histories in the state. Health systems like Johns Hopkins Medicine and University of Maryland Medical System also sponsor analytics roles, particularly in clinical and operational data work. Checking Labor Condition Application disclosure records through OFLC shows which firms file most actively.
Which visa types realistically fit data analytics consultant roles in Maryland?
Data analytics consultant roles typically qualify as specialty occupations requiring a bachelor's degree in a directly related field such as statistics, computer science, mathematics, or information systems. The H-1B visa is the most common path, with initial status up to three years extendable to six. H-1B1 visa applies to Chilean and Singaporean nationals, and E-3 visa applies to Australian nationals, both also requiring specialty occupation eligibility. F-1 students may use OPT or STEM OPT if their degree is STEM-designated, with STEM OPT providing 24 additional months. Employer-sponsored EB-2 or EB-3 green cards are available for longer-term positions.
How to find data analytics consultant visa sponsorship jobs in Maryland?
Migrate Mate lists data analytics consultant roles specifically at employers with verified visa sponsorship histories in Maryland, letting you focus your search on companies that have filed for similar positions before. Filtering by the Baltimore-Washington corridor surfaces the defense contracting and health tech firms that drive most analytics hiring in the state. Searching Migrate Mate by role and location is a practical starting point for international candidates targeting Maryland opportunities.
Which cities in Maryland have the most data analytics consultant sponsorship jobs?
Bethesda and Rockville anchor the highest concentration of analytics sponsorship activity, driven by federal health agencies like NIH and FDA along with the contractors that support them. Baltimore follows closely, with strong demand from health systems, financial services firms, and cybersecurity companies. Columbia and Greenbelt also see meaningful activity given their proximity to federal campuses and established tech corridors along the I-270 and Route 1 corridors.
Are there state-specific factors that affect visa sponsorship for data analytics consultants in Maryland?
Maryland's heavy federal contracting presence means many data analytics consultant roles require security clearances, which can complicate sponsorship for candidates not yet authorized to hold them. Employers in the defense and intelligence sectors often prefer to sponsor candidates already in the pipeline for clearance eligibility. The state's university system, including University of Maryland College Park, also generates a consistent pipeline of international STEM graduates who pursue OPT and STEM OPT placements with Maryland-based analytics employers before transitioning to H-1B sponsorship.
What is the prevailing wage for sponsored data analytics consultant jobs in Maryland?
U.S. employers sponsoring a visa must pay at least the prevailing wage, which is what workers in the same role, area, and experience level typically earn. The Department of Labor sets this rate to make sure companies aren't hiring foreign workers simply because they'd accept lower pay than a U.S. worker. It varies by job title, location, and experience. You can look up current prevailing wage rates for any occupation and location using the OFLC Wage Search page.