Our talented Clinical Research Managers, Clinical Research Associates, Clinical Trial Assistants and Medical Writers will help you operate your clinical trial.
Together the Clinical Operations team members has an average of 13 years experience from the pharmaceutical industry, CROs, healthcare and academia in the development and use of pharmaceutical products, medical device and functional food. We have acquired the best of knowledge to provide your company with the expertise you need to operate your clinical trial.
Our Clinical Research Managers (CRMs) skilfully manage vendors and study teams to ensure effective start-up and regulatory compliant conduct of your clinical trial in close collaboration with you as our customer. Read more about our project management services.
Our Clinical Research Associates (CRAs/Study Monitors) ensure the quality of your clinical trial by practicing risk-based monitoring. They identify, assess, monitor and mitigate risks that could affect the safety of the subjects or the quality of your clinical trial. Read more about our CRA and CTA services.
Our Clinical Trial Assistants (CTAs) play a central role in providing structured study files for your study documentation and support Clinical Operations in our day-to-day activities.
Our Medical Writers proactively coordinate the cross-functional development of your clinical study protocol and know how to effectively and clearly analyse and communicate the clinical output from your study, orally and in writing. Read more about our medical writing services.
Mikaela Lundell, Director Clinical Operations