Join us where collaboration between scientists, clinicians, biostatisticians, data scientists, and IT experts is producing the highest quality results.
What can we do for you?
Pharmacovigilance and Medical Monitoring
Medical review and consultancy along with case processing, safety reporting, analysis, and submissions.
Protocol Development and Data Management
From protocol document review to enable consistency, completeness and clarity, to site support, data cleaning and quality control.
Investigator, Site and Patient Services
From site identification, selection, activation, and monitoring, to patient recruitment, screening, blinding and management, we have the support services needed for your trial.
Statistical Design and Analysis
From protocol design and pre-study feasibility, to reporting, Data and Safety Monitoring Board (DSMB) support and manuscript preparation.
Global Regulatory Affairs
Emmes can help you navigate the investigational new drug, device and biologics regulatory pathways toward a successful product launch.
Medical Writing
Including protocols for both interventional and non-interventional trials, data management plans, study reports, manuscripts, posters and presentations.
Quality Assurance
Ensuring operations follow established procedures through auditing of study data, sites, laboratories, 3rd party vendors and CROs.
Schedule a Meeting
Please contact us
Careers
Careers