Join Our Team

We are always looking for new talent with the drive to make an impact on the medical community. Does this sound like you? Apply to join our team.

SAS Programming Manager

The Manager, SAS Programming oversees statistical deliverables, creates and performs programmatic review of analysis data sets and Tables, Listings, and Figures (TLFs), and expedites the preparation of regulatory submissions. The Manager supervises the SAS Programming team, is responsible for meeting client timelines, and supports the development of programming standards to improve efficiency and quality. Learn more…

Regulatory Affairs Associate

The Regulatory Affairs Associate has responsibility for assistance in regulatory aspects of the company’s clinical studies from concept to completion, including CERs, clinical investigation plans, clinical study reports, regulatory submissions and supplements, and other regulatory filings. Learn more…

Quality Assurance Lead

The Quality Assurance Lead has responsibility for developing and managing testing methodologies, frameworks, and metrics for the technology arm of our Clinical Research Organization. Requires a solid understanding of web application architecture. Learn more…