Drive the execution of clinical monitoring activities, ensuring compliance with regulatory standards, conducting site visits, and managing site personnel for successful trial outcomes while providing thorough documentation and communication.

Drive growth by leveraging CRO sales experience to cultivate client relationships, enhance market presence, and support strategic initiatives for clinical research solutions across the western United States. Remote with travel as needed.

Join our team to enhance regulatory compliance and quality assurance. Drive GxP project implementations, support clients, and develop expertise in evolving regulations. Your contributions will directly impact project success and client satisfaction.

Lead the charge in quality assurance and regulatory consulting, delivering expert guidance on GxP compliance, managing projects, driving strategic initiatives, and enhancing client satisfaction while staying abreast of industry standards and innovations.

Lead the charge in advancing Class III medical device projects, overseeing cross-functional teams through design, regulatory, and commercialization phases to ensure compliant, market-ready implants are delivered on time and within budget.