CRA-Partner is a network of independent Clinical Research Consultants, who all have extensive CRA, clinical trial management and medical writing experience.
As independent Clinical Research Consultants, we provide clinical trial monitoring and project/trial management as well as medical writing services to biotech and pharmaceutical companies.
Our core business is to provide experienced and skilled assistance within the clinical operations and clinical research area of clinical trials; from trial set-up and planning, through execution and all the way to close down and reporting of trial results.
We are ready to act as your flexible colleague and we offer a range of services including on-site monitoring, trial management, project management and medical writing.
Staff experience and continuity is crucial for carrying out a trial in a successful and trustworthy manner. This is what CRA-Partner offers you.
Working with a CRA-Partner means contracting and working directly with the responsible consultant, ensuring a personal match and clear expectations. You contract an individual consultant, but with the advantages of having a network and back-up from other CRA-Partners.
Depending on your needs we can act as your partner during the full trial period or during a shorter period.
If you are in need of skills and resources for your clinical trial projects, please contact us.