Founded in 1994, CenterWatch is a trusted source and global destination for clinical trials information for both professionals and patients. Located in Boston, CenterWatch provides proprietary data and information analysis on clinical trials through a variety of newsletters, books, databases, and information services used by pharmaceutical and biotechnology companies, CROs, SMOs, and investigative sites involved in the management and conduct of clinical trials.
CenterWatch offers several services and resources specifically to patients. With our Clinical Trial Listing Service we are able to provide patients with unbiased information on clinical trials, with a clinical trial database that contains thousands of currently enrolling trials. Information on drugs and new medical therapies are available to review. CenterWatch also provides patients with health and educational resources about clinical trials and other health information.
The Society for Clinical Research Sites was founded in 2012 in response to the growing need for a trade organization to represent the voice of research sites within the clinical research enterprise. Christine Pierre, the founder of the Site Solutions Summit, was motivated, along with other research professionals, to provide sites with resources, mentorship, and new ideas through a membership organization dedicated to providing the sites both a voice and community.
Now, with SCRS a reality, the ability to make a positive difference for the clinical research sites and their industry partners can be realized through giving the sites a unified voice and community. Pierre describes the origin of SCRS:
“We are all aware that as an industry we currently have an unsustainable model – for all stakeholders. As sites represent the largest number of providers to the industry, their impact on this process cannot be underestimated. Sites, which have long been the silent partner in the research enterprise, will no longer be passive participants. Now is the time for sites to become part of the dialogues and solutions through the voice of SCRS. I am confident we can attain operational excellence while, at the same time, ensuring study volunteers safety.”
Unify and amplify the voice of the global clinical research site community for site sustainability.
Advocate. SCRS will, on behalf of its site members, publicly comment on issues relevant to the clinical research industry. SCRS will work to maintain a presence in conversations with other groups and organizations to ensure the site’s perspective and voice is present as important decisions and debates are occurring.
Connect. SCRS provides a unique opportunity to sites and industry stakeholders to interact with companies and individuals across multiple sectors of the industry. The SCRS community creates an environment that supports meaningful partnerships all year long and not just at meetings.
Educate. SCRS’ knowledge platform creates the foundation for informed action, where industry leaders can analyze their most efficient programs, fresh voices can introduce proven innovations, and established experts can debate different interventions. SCRS and its members provide each other with a constant flow of new solutions and lessons learned.
Mentor. Recognizing both the importance of SCRS’ emphasis on excellence and the reality that new sites enter the industry each day, site members will offer to mentor to other site members.
The Association of Clinical Research Professionals (ACRP) is the primary resource for clinical research professionals in the pharmaceutical, biotechnology and medical device industries, and those in hospital, academic medical centers, and physician office settings. Headquartered in Alexandria, Virginia, ACRP was founded in 1976 to address the distinct educational and networking needs of research nurses and others who supported the work of clinical investigations. With its own professional society came the recognition of a new distinctive profession — that of the clinical researcher. More than 35 years later, ACRP is a global association comprised of the largest community dedicated to clinical research and development.
iCardiac Technologies, Inc., is the industry’s most innovative core laboratory for cardiac safety and respiratory services. We have introduced multiple breakthrough innovations to the cardiac safety industry, including our High Precision QT and Early Precision QT methodologies. iCardiac’s precision-optimizing cardiac safety assessment methodology has set a new standard for precision and accuracy in all phases of clinical trials. We have run some of the largest global respiratory studies that have ever occurred in the industry, and our unique platform ensures that subjects are not inappropriately included or excluded from studies. iCardiac serves 8 of the top 10 global pharma, as well as numerous small and mid-sized pharma and biotech companies. Our team members are active contributors to several FDA working groups that are advancing the field of drug safety.
New Hope Clinical Research
3101 Latrobe Dr
Charlotte, NC 28211
Phone : 980-228-9616
Fax : 980-226-5843
- Monday – 8:00 am – 5:00 pm
- Tuesday – 8:00 am – 5:00 pm
- Wednesday – 8:00 am – 5:00 pm
- Thursday – 8:00 am – 5:00 pm
- Friday – 8:00 am – 5:00 pm
- Saturday – Closed
- Sunday – Closed