CCBR-Aalborg has existed as independent Clinical Research Center since 1995 with a capacity of 1300 patients per year. CCBR-Aalborg is fully operational in phase I to phase IV trials. During its many years of operation CCBR-Aalborg has established a strong network and has a large database to recruit both healthy volunteers and patients with various diseases. The very high retention rate in various clinical trials has been very well recognized by our clients.
In 2009 the phase 1 unit was further developed and renovated in close collaboration with the CRO C4Pain to meet our clients demand for a unit that can handle phase I trials from proof-of-concept and further through Phase Ib. Our main target areas are pain, osteoporosis, osteoarthritis, diabetes, dyslipidemia, Irritable Bowel Syndrome and constipation. New upcoming target areas includes Alzheimer’s disease.
CCBR, Aalborg Hobrovej 42 D 2. sal , 9000 Aalborg Denmark
Phone: +45 9633 4720 fax: +45 9813 9048
Managing Director of Clinical Research Center: Bettina Storgaard Nedergaard
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Bettina S. Nedergaard, MD, Ph.D. | |
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Managing Director of Clinical Research Center & Physician |
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Jens Vang Andersen, MD | |
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Physician |
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Ole Svendsen, MD | |
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Physician |
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Sonja Snel, MD | |
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Physician |
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Carina Widén Zakhary, MD | |
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Physician |
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Lene Rubiano | |
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Study Coordinator & Local head of QC |
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Rikke Würtz | |
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Study Coordinator |
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Mette H. Skaksen | |
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Study Coordinator |
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Lene Nielsen | |
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Study Coordinator |
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Hanne S. Sørensen | |
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Study Coordinator |
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Mette N. Jensen | |
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Study Coordinator |
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Sofie Gradin | |
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Study Coordinator |
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Brit Nielsen | |
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X-ray Technician, Study Nurse |
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Merete Christensen | |
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DEXA Technician & Laboratory Technician |
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Louise Dyg | |
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DXA Operator Radiograf |
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Susanne Henriksen | |
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Laboratory Technician |
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Lone Kristensen | |
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Laboratory Technician |
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Maria Elisabeth Jensen | |
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Laboratory Technician |
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Asiah Rahi | |
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Clinical Assistant |
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Lene Kirch | |
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Secretary |
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Lise Lotte Husum | |
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Secretary |
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Susanne Hybholt | |
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Secretary |
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Ulla Schmitz | |
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Office Assistant |
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Maiken Nielsen | |
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Office Assistant |
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
