Expert Clinical Trial CRO: About PRC Clinical
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Who We Are
Who We Are
PRC Clinical began providing clinical trial CRO services in 2003 offering clinical research consulting to pharmaceutical, biotech, and medical device and diagnostic sponsors. Over the past two decades, PRC has grown from a small consulting firm to a trusted CRO partner offering functional and full-service clinical operations and integrated data management, biostatistical and pharmacovigilance teams specialized in personalized project management, timelines and quality deliverables. Our signature services of project oversight, site management, monitoring and eTMF document management focus on de-risking clinical studies to ensure that our sponsors meet enrollment goals on time with the highest data integrity and quality.
Our Mission
PRC brings lifesaving therapies to patient populations by providing competent expertise in clinical trial services and management to smaller biotech, pharma and device sponsors, giving them a competitive advantage in moving through the trial and approval process.
Our Vision
At PRC Clinical we believe that our success is directly tied to the success of our customers, employees and partners. That’s why we strive to provide the best possible service and support to help them achieve their goals. We are committed to building strong, long-lasting relationships based on trust, respect and mutual benefit. Thank you for choosing PRC Clinical as your partner in success.
Our Team
Our leadership and executive management team have spent their entire careers getting here. Made up of industry veterans, the team has decades of combined experience in clinical research, business and quality management.
Curtis Head
CEO & Co-Founder
Tony Taricco
President & Co-Founder
Shari Burgess
Vice President
Kara Lee Rimkus
Quality Assurance
Employee & Contract Staff
PRC Clinical nurtures a hands-on culture where employees and contract staff are empowered to work toward their career goals.
Our core study teams are generally full-time employees, providing the necessary stability to clinical studies across the day-to-day project management.
Contracted staff on the other hand, give our studies the benefit of being highly flexible to adjust staff when and where it is needed. Contract staff are afforded many of the same benefits of working at PRC, and because this team is contracted for our sponsor’s studies — aware of the workload, start and end dates — there is far less turnover than many other CROs.
PRC Clinical provides opportunities for career advancement as well as flexible work hours and many other attractive options — see what we can do together.
Open Roles
Whether providing overall clinical trial management, North American support or part of global studies, remote or site monitoring, PRC Clinical knows that delivering expert clinical trial services and high-quality data requires hands-on care. We’re the right size — right fit for understanding your needs, executing your protocol, finding ideal sites from our extensive network and maintaining the close contact that keeps research on schedule and on budget.