Emmes information
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$22.60 - $27.29
13% of jobs
$27.29 - $31.99
9% of jobs
$36.69 is the 25th percentile. Wages below this are outliers.
$31.99 - $36.69
3% of jobs
$36.69 - $41.39
1% of jobs
$41.39 - $46.09
5% of jobs
The median wage is $50.54 / hr.
$46.09 - $50.79
20% of jobs
$50.79 - $55.49
18% of jobs
$58.30 is the 75th percentile. Wages above this are outliers.
$55.49 - $60.18
10% of jobs
$60.18 - $64.88
5% of jobs
$64.88 - $69.58
9% of jobs
$69.58 - $74.28
6% of jobs
How much do emmes jobs pay per hour?
As of Aug 18, 2026, the average hourly pay for emmes in the United States is $49.88, according to ZipRecruiter salary data. Most workers in this role earn between $36.78 and $58.65 per hour, depending on experience, location, and employer.
Emmes is a global contract research organization (CRO) that provides clinical research services to biopharmaceutical companies, government agencies, and non-profit organizations. They specialize in designing and managing clinical trials, data management, biostatistics, and regulatory support across various therapeutic areas. Emmes helps clients navigate the complexities of clinical development from study design to regulatory submission, ensuring high-quality data and compliance with industry standards. Their expertise supports the advancement of new medical therapies and interventions.
Clinical research professionals at Emmes are often involved in diverse projects, including multi-center clinical trials, epidemiological studies, and public health research, frequently in collaboration with government agencies and academic institutions. This exposure allows team members to gain experience across various therapeutic areas and study phases, enhancing both their technical and project management skills. The collaborative environment at Emmes fosters ongoing learning and mentorship, supporting career advancement into roles such as project management, data analysis, or regulatory affairs.
To thrive as a Clinical Research Associate (CRA), you need a solid background in life sciences or a related field, often supported by a bachelor’s degree and relevant clinical research experience. Familiarity with Good Clinical Practice (GCP), electronic data capture (EDC) systems, and regulatory compliance is crucial. Strong attention to detail, organizational skills, and effective communication set top performers apart. These competencies ensure the integrity of clinical trials, regulatory adherence, and successful collaboration with research teams.
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