Bio Pharma / Healthcare Services
We provide sponsors with an experienced, skilled, and proactive clinical trial management resources to efficiently manage and complete phase I through phase III clinical trials on-time for bio-pharmaceutical, medical devises companies, clinical research sites, and CROs.
Our consultants/employees have experience working in multiple Therapeutic Areas at various capacity, varying from Medical Writing, Clinical Operations, Medical Monitoring, Data management and Quality.
Our flexible sourcing strategy provides resources with no extra costs to sponsors/partners. We can provide single consultant or team of consultants to complete your clinical trials from feasibility, start-up to study close out on-time. Our resources can be placed at sponsors/partner site or offsite / offshore at our locations or can work remote at our US office. We offer our consultants for permanent positions and long and short temporary positions.
Below are some of the resources listed that we could offer to our partners.
Clinical Trial Managers / Clinical Project Managers
Vendor Managers
Clinical Research Associates
Clinical Research Coordinators
Clinical Trial Associates / Clinical Trial Assistants
Study Start-up specialists
Site Contract and budget negotiation Associates / Managers
Clinical Drug Associates
Regulatory Affairs Associates
Clinical Data Associates
Clinical Data Managers
Statistical Programmers
Biostatisticians
Medical Writers
Medical Monitors
Service Offerings
Consulting
Site Selection
Project Management
Site Monitoring
Quality Assurance
