BIOTRONIK seeks a Principal Clinical Research Analyst in Tustin, CA to lead clinical evaluation and regulatory strategies for Class III devices. You will drive CER/PMCF programs, perform evidence analyses, and collaborate with Regulatory, Quality, and Engineering teams to ensure lifecycle regulatory compliance.
The role requires extensive EU MDR experience, strong scientific writing, and cross-functional leadership. Hybrid onsite work at the Tustin facility is offered.
#J-18808-LjbffrSenior Clinical Research Lead — EU MDR & Class III Devices in tustin at Unknown Company
This position is listed as full time and hybrid.