Medpace
Posted 98 days agoVerified live 2d ago
Statistical Analyst I
Brief overview
Cincinnati,Ohio,United StatesIn-person
MastersOr in progress
87 H-1B approvalsDept. of Labor
15 green cardsCertified filings
About the company
Medpacemedpace.com
Medpace, Inc., a clinical research organization, provides clinical development services for pharmaceutical and biotechnology
Visa sponsorship history
4 years sponsoring, last filed FY2026
Data powered by U.S. Department of Labor. This does not guarantee sponsorship for this specific role.87H-1B approved
95%approval rate
46new H-1B hires
15PERM certified
$120,000median wage / yr
H-1B Petition ApprovalsVisas USCIS actually granted: the strongest sign the company sponsors.
202319
202431
202530
20267
LCA Certified ApplicationsAn early filing step, not a visa approval: it signals intent, not confirmed sponsorship.
20235
20241
20255
20262
Green Card (PERM) FilingsCertified green card filings: a long-term commitment to international hires.
20231
20246
20257
20261
Top sponsored roles
Statistical Analyst IIISoftware Engineer IIIBioinformatics Scientist IIIBiostatistician IISoftware Engineer I
Sponsored employees from
ChinaBangladesh
Job description
Summary
Medpace is a full-service clinical contract research organization (CRO) that provides Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. They are seeking a Statistical Analyst I to write statistical programs for analysis datasets and communicate project requirements to ensure data suitability for analysis.
Responsibilities
- Write statistical programs for use in creating analysis datasets, tables, listings, and figures
- Review analysis plans for appropriate methods
- Program study analyses and review study results; and
- Communicate the project requirements for cleanup and data capture to ensure the key study variables are suitable for analysis
Skills
- Master's Degree in Statistics/Biostatistics required
- SAS and / or statistical programming experience
- Knowledge of databases and data management process
- Knowledge of statistical methods commonly used in pharmaceutical clinical trials
Qualifications
Must Haves
- Master's Degree in Statistics/Biostatistics required
- SAS and / or statistical programming experience
- Knowledge of databases and data management process
- Knowledge of statistical methods commonly used in pharmaceutical clinical trials
Benefits
- Flexible work environment
- Competitive PTO packages, starting at 20+ days
- Competitive compensation and benefits package
- Company-sponsored employee appreciation events
- Employee health and wellness initiatives
- Community involvement with local nonprofit organizations
- Discounts on local sports games, fitness gyms and attractions
- Modern, ecofriendly campus with an on-site fitness center
- Structured career paths with opportunities for professional growth
- Discounted tuition for UC online programs
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