CRAs/Monitors provided anytime anywhere from our extensive global database. Before being accepted onto our database, each CRA is required to prove a thorough understanding of their therapeutic areas, as well as strong GCP knowledge.
Local regulatory trial start up experts can be supplied on an ad hoc basis to ensure a smooth start with transparent timelines to your study on a country by country basis across the globe.
Data entry staff can be provided across all European countries for short or long term studies (minimum 3 months). The data entry staff work in harmony with the site teams to ensure deadlines are met.
Clinical teams consisting of Project Managers, CRAs and Clinical Trial Assistants can be provided to give an alternative solution to engaging with CROs. The teams can either work in house or from local offices in a particular country.
Biometrics team solutions also provide an alternative to engaging with full CRO solutions. Experienced Data Managers and Statisticians will work hand in hand with the Clinical team in house or from local offices.
Permanent or contract staff recruitment in all areas of the industry with particular expertise in supplying Clinical, Regulatory, Biometrics and Technology staff.
Since our incorporation in 2011, we have built up contacts across all continents.
We have collaborations with industry groups across various countries to ensure we provide bespoke tailored solutions to excatly suit your needs.
We advertise on a global scale to ensure we hire the best and most appropriate teams.
Call us on 01483 60 88 50 to discuss the solution to help you.
We will take time to research your requirement in depth and provide the right solution.
We will never promise something we cannot deliver.
We will ensure transparency at all times
We will always provide the lowest possible cost to you, without unecessary overcharging.
We will always offer you a smile and you will enjoy dealing with us.