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.

Clinical Project Manager

Under the direction of the Associate Director, Clinical Operations or Senior Clinical Project Manager, the Clinical Project Manager has responsibility for the comprehensive management of clinical studies and communication with study sites and sponsors. Occasional travel may required. The Clinical Project Manager may also participate in the development of SOPs, and internal monitoring processes.

Clinical Research Associate

Under the direction of the Senior Manager, Clinical Monitoring, the CRA has responsibility for the comprehensive monitoring of clinical study sites. This includes the responsibility to verify that the rights and well-being of human subjects are protected and that the trial is conducted in compliance with GCP and with all applicable regulatory requirements. The CRA I will also assist with other project management and site management activities, as needed. Travel is required.

Clinical Data Manager

Under the direction of the Senior Vice President, Clinical Sciences, the Data Manager has responsibility for data management tasks required for assigned clinical projects. Travel is not required.

Core Laboratory Research Associate

Under the direction of the Associate Manager, Core Laboratory, the Research Associate, Core Laboratory has responsibility for the quantification and measurement of core laboratory studies. This may include web-based quantification systems such as TeraRecon. The Research Associate, Core Laboratory shall conduct their work in compliance with GCP and with all applicable regulatory requirements. Local travel may be required.

Regulatory Affairs Writer

The Regulatory Writer will be responsible for the writing and editing of various regulatory documents intended for global regulatory bodies. The candidate will work under the direction of the Regulatory Affairs Manager and in collaboration with the Regulatory Strategy Department. There will be opportunities to work with leaders in the medical device field on innovative and groundbreaking new products across multiple clinical areas. Less than 5% travel maybe required.

Clinical Project Lead

Under the direction of the Senior Project Manager, the Clinical Project Lead has responsibility for assisting the project team with the comprehensive management of clinical studies and communication with study sites and sponsors. Occasional travel may be required.