All CRA-Partner consultants have a degree in Life Sciences and have specialised in different areas highly relevant for clinical trials, such as planning, monitoring, patient recruitment, GCP training, clinical trial management and medical writing.
All consultants have extensive experience within clinical research, including CRA and medical writing experience, which we believe is the backbone of the activities within a clinical research department for trial planning, execution and reporting. If you are concerned with effective planning, execution and reporting of high quality clinical trials within agreed timelines, CRA-Partner offers the skills and experience needed.
Since 2005, CRA-Partner has successfully conducted clinical research and has worked for more than a dozen different biotech and pharmaceutical companies. Geographically our experience includes monitoring of clinical trials in Denmark, Norway and Sweden, project management throughout Europe and the United States of America as well medical writing services in phase I-IV trials within a wide range of therapeutic areas.
We are located in the Copenhagen area in Denmark.