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