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Anette Vierning is Director of Clinical Operations and Performance Services. She has a background as a registered nurse, working in neonatal intensive care and as a Health care visitor, followed by 10 years of experience within clinical research, backed up by exams and courses within Clinical Drug Development and a Diploma in GCP monitoring. Her past experience in CCBR comprises coordinating and auditing clinical research centers, project management and serving as a Clinic Manager of CCBR Ballerup, Denmark.
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| This e-mail address is being protected from spambots. You need JavaScript enabled to view it. | Phone | +45 9633 4700 |
Working with CCBR speeds up and drives efficiencies in clinical trials by offering greater numbers of patients across fewer sites
A Global Footprint covering more than 20 dedicated Clinical Research Centers in high density population areas
Uniform SOPs enable the tightest possible adherence to study protocols and consistency across all CCBR sites
Real-Time tacking of subject enrolment and trial progress ensures sponsors have the most up to date information, all of the time
Centralised, standardised billing affords better visibility into trial costs for sponsors
