Trial Experience
CUREM has experience across all phases of development and is recognized for exceptional quality and accuracy. Our team recently completed a phase III trial in 919 subjects and 125 clinic sites with an electronic trial data capture system completing database lock in 3 days from last patient visit.
Team Experience
Having worked with
each other for over 10 years, CUREM staff quickly transition to a
cohesive extension of the sponsor’s team. Our medical writer
has over 20 years of clinical trial experience writing for
pharmaceutical and biotechnology companies. Our lead biostatistician is
considered an expert in his field having worked in positions of
increasing responsibility for a major pharmaceutical company for over
20 years.
CUREM CRAs average over 10 years experience and nearly 80% are
registered nurses. Our data managers average 8 years
experience with our lead data manager having over 13 years experience
in the roles of data manager, monitor and clinical study manager.
Testimonials
“CUREM saved us $800,000.00 compared to a similar study monitored by a large CRO.”
“CUREM qualified over 100 sites in a 12 week period and came in 50% below budget on travel expenses.”
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Therapeutic Expertise
CUREM Research Partners colleagues are highly regarded for their depth and breadth of clinical reserach experience. Therapeutic area expertise of our staff includes, but is not limited to, experience in the following:
- Oncology
- Cardiovascular
- Ophthalmology
- CNS
- Stroke
- Women’s Health
- Gastroenterology
- Hepatitis
- Asthma
- Diabetes
- Hemophilia
- Renal Failure
- Infectious diseases
- HIV
- Genitourinary
- Pain management
- Psychiatry
- Pediatric studies
- Dermatology
- Parkinson’s
- Alzheimer’s
- Insomnia
- Otitis Externa
- Erectile dysfunction
- Endometriosis
- Sepsis
- Ulcerative colitis
To find out how our company can help you achieve your goals in your clinical trial research studies, call 734-253-2632 today. Or, email us at info@curemresearch.com.