For Sponsor and CRO Services
SERRG helps you bring your product to market with superior data and confidence.
SERRG is dedicated to bringing your cutting edge therapies to the marketplace in less time and for less money. That’s because we provide you with ethical, quality-oriented, enthusiastic, and experienced clinical research data in an expedited and efficient manner. We manage your projects with the utmost attention and we are committed to ensuring the successful outcome of your clinical investigation.
Expert Site Management
We manage and expedite site identification, qualification, initiation, and budget/contractual negotiations. Our internal management and operating procedures are specifically designed to provide you with multiple and highly-qualified sites that meet your specific criteria. Because we only present those sites that meet your self-defined needs, you can significantly reduce the time and resources required to evaluate and qualify a site or Principal Investigator.
Established Relationships and Networks:
We have a vast network of investigators that will meet your specific criteria, so that your time and resources are saved during the initial site identification, screening, and qualification of our investigators. We also have excellent working relationships with many quality CROs. Because of these established relationships, communication is greatly enhanced. Additionally, because the CRO may have previously worked with a particular site, they are familiar with its capabilities and past performance. This can significantly reduce time and resources expended during the site identification and qualification process. Having an established relationship between the monitor and site can also reduce monitoring time and expense.
Experienced Staff:
We assign a research coordinator to your study to centralize communication. This increases efficiency by reducing the time you typically spend answering similar site-generated questions. All of the Investigators in our network are highly experienced clinicians and researchers and must meet our stringent criteria of medical knowledge, experience and superior skills and ethics.
Contractual and Budgetary Management:
Budgetary and contractual discussions are always centralized, thus minimizing lengthy negotiations for each site. Upon agreement of a budget (which is applicable across all sites), a clinical trial agreement can typically be executed quickly.
SERRG’s Highlighted Services:
- Quality sites established with one phone call
- Phase II through Phase IV studies managed from start to finish
- Large database of highly skilled, experienced and enthusiastic Investigators
- Dedicated, full-time, and experienced Certified Clinical Research Coordinators
- Access to large patient populations with cultural diversity
- Efficient and centralized contract and budget resolution
- Strong working relationships with local and central IRB’s and laboratories
- Track record of consistently meeting or exceeding enrollment goals
- Aggressive patient recruitment including advertising and marketing materials to support local site’s own efforts
Proven ability to successfully conduct the most challenging studies - Supporting member of ACRP and APPI
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