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Coastal Carolina Research Center (CCRC) believes these words characterize our strengths; we look forward to working with you in the future.
- Performance – Proven enrollment and retention rates in multiple therapeutic areas and clinical trial models.
- Quality – Low query rates, thorough source documentation, and proficiency with numerous clinical research tools (ie: EDC, IVRS, e-diaries, IRBs, Clinical Labs)
- Experience – Coastal Carolina Research Center is a multi-therapeutic research center that has conducted over 300 clinical trials in many different indications. CCRC’s 7 primary study coordinators have a combined 80 years of research experience. Dr. Strout, CCRC’s medical director; provide leadership and 12 years of dedicated clinical research experience (>200 clinical trials). Our support staff, including Lab Manager and staff Dietician, contributes additional abundant clinical research experience. For details visit our Sponsors Experience and CRO Experience pages.
- Integrity – Honesty, in the event we make a mistake, this is communicated in a timely manner to the sponsor and careful consideration is given to all participants before they enroll into one of our clinical trials.
- Humility – At CCRC we know what our strengths are and, more importantly, we know what our weaknesses are. Study feasibility is vital to our success; if we do not believe we would conduct a study well we will gladly decline consideration. In general we decline more studies then we accept.
- Passion – The staff here at CCRC truly enjoys what we do for a living and understand the valuable service we provide the Lowcountry community. All clinical staff are HAZMAT and BCLS certified.
- Diversity – CCRC’s research population is diverse according to age, gender, race and socio-economic status. We fully understand and appreciate that clinical research affects everyone.
- Customer Service – Excellence in serving our local clinical research volunteers and our clients is priority and is constantly reinforced, as witnessed by our Patient Testimonials. All clinical staff HAZMAT and BCLS certified.
- Leadership – CCRC accepts the responsibility of providing leadership and education in the Charleston metro area to be the "Lowcountry's Resource for Medical Research"
- Community - The Charleston area is a very conducive area in which to conduct clinical research. Generally the area has a "positive" attitude about clinical research and wants to fully understand the "active" role they may play in the process.
- Facilities & Equipment – CCRC has two thoroughly equipped research sites. Click here to read a complete description of our facilities.
Coastal Carolina Research Center Facts:
- Two site locations: Mt. Pleasant and Goose Creek
- GCP Trained and Certified Clinical Staff
- CCRC utilizes Central IRBs / Regulatory submission within 48 hours
- CLIA certified lab on site
- Drug Storage is on site in climate controlled, secure room
- Freezers available on site including -70 degree Celsius
- Refrigerated Centrifuge on site ECG available on site / Analog lines
for data transmission
- Automatic Back-Up Generator installed
(capacity to power entire office for 8 days)
- Monitor Rooms on site with Internet Access
- Experienced with multiple EDC, IVRS, and E-diary vendors
- Access to any diagnostic study requirements
- Charleston area – positive attitude towards medical research
- Successful FDA audits
PI Experience
Sponsors Experience
CRO Experience
The content in this website should serve all potential Sponsor or Contract Research Organizations (CROs) with enough information to merit our consideration as a clinical research investigator partner. Should you have any questions or concerns please contact:
Nathan Morton
Director of Business Development
Phone #: 843-856-3784
Fax #: 843856-3788
Email: nmorton@coastalcarolinaresearch.com
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