Our team’s objective is to provide you with experienced, qualified clinical research sites for a successful and timely completion of a study.

We create well-established working relationships at each site and implement our Strategic Clinical Study Management Plan to ensure excellence and precision throughout the life of the study.

  • We engage in routine communication with all of our sites.
  • We provide study update reports to our sites.
  • We review enrollment goals and discuss recruitment strategies.
  • We schedule regular meetings with both the CRC and Physician.

Our Sponsor services include:

Site Qualification Development

  • Pre-qualify sites to ensure study is a good fit and enrollment goals can be met
  • Site information packets provided to CRA
  • Site visit preparation (e.g. protocol and equipment review)
  • Site visit date and time coordination

Document Processing

  • Regulatory document completion within 7-10 business days
  • Centralized contract and budget negotiations within 7-10 business days
  • Central IRB submission

Site Management

  • Thorough up-to-date CV, licensure and training certification review
  • Standard Operating Procedures (SOP) binders
  • Patient recruitment marketing services
  • Identify process improvement areas and implementation

Sponsors/CROs relationships

Abbott Merck
Abbvie Novartis
Alcon Novo Nordisk
Amgen Parexel
Bausch and Lomb Pfizer
Boehringer Ingelheim Pharma-Olam
Chiltern Purdue
Eli Lilly Quintiles
Eyegate Salix
Forest Smith and Nephew
Furiex SGS
Genentech Symbio
GSK Synergy
Inotek Takeda
Inventiv UBC
Medpace Zimmer

Synergyst Research Group, llc.
Corporate Office
4242 Medical Drive, Suite 5100
San Antonio, TX 78229

Mailing address
2313 Lockhill-Selma Road #245
San Antonio, TX 78230

Synergyst Research Group / Discovery Clinical Trials Honored for Third Year in a Row on the Inc. 500|5000 List of America's Fastest-Growing Private Companies.
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