Accelerates Hiring & Plans to Open Office in Raleigh-Durham, North Carolina
SOUTHBOROUGH, MA – June 27, 2016 – Veristat, a full service Clinical Research Organization (CRO) with over 20 years of experience, announced today that it is continuing its accelerated growth and geographic expansion with the opening of an office in Raleigh-Durham, North Carolina. In addition to this newly planned North Carolina office, Veristat has additional North American-based offices in Southborough, MA, Cambridge, MA, San Bruno, CA, Montreal, Canada, and its European office in Glasgow, UK. The new office, scheduled to open in the fall of 2016, will support the company’s accelerated growth by engaging an experienced talent pool and providing local support to Veristat’s clients in the area.
Veristat has hired many talented clinical research professionals in North Carolina,” stated Patrick Flanagan, Chief Executive Officer of Veristat. “The Raleigh-Durham area has a population that includes a very experienced and professional CRO community. We have hired and will continue to hire very talented individuals to grow our team of biometrics and clinical operations professionals. Having a local office will facilitate the expansion of our team and allow us to better serve the clinical development needs of our clients.
Veristat currently has Clinical Operations, Biostatistics, SAS Programming, Data Management and Business Development/Account Management team members based in North Carolina. The Company is currently hiring professionals for all of its business units, including Clinical Operations, Biometrics, Medical & Regulatory and SG&A. Veristat will rapidly accelerate hiring as the office opens later this year.
Veristat is an innovative full-service, science-focused clinical research organization (CRO) with over 20 years of experience in supporting clinical trials and regulatory submissions for pharmaceutical, biotechnology, and medical device companies. Veristat offers comprehensive clinical development services, including biostatistics, statistical programming, medical writing, clinical monitoring, project management and data management, for a single study or an entire clinical program, as well as preparation of integrated summary documents and submission-ready CDISC data for regulatory filings. Due to Veristat’s unwavering commitment to scientific integrity, client focus and exceptional performance, long-lasting client relationships are our hallmark. For more information, please visit www.veristat.com.
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