Clinical Regulatory Liaison • Mid-Level

Who you are

You have a strong background in clinical regulatory affairs and quality assurance, with experience in reviewing clinical complaints and ensuring compliance with regulatory requirements. You are detail-oriented and possess excellent analytical skills, allowing you to effectively investigate and resolve clinical issues. Your ability to communicate clearly and work collaboratively with cross-functional teams is essential in this role. You are self-motivated and driven to make a positive impact on patient care through your work. You understand the importance of maintaining high standards in clinical quality and are committed to continuous improvement.

What you'll do

In this role, you will support the Clinical Services Quality Assurance team by maintaining and enforcing iRhythm’s Clinical Quality Assurance System. You will review and evaluate clinical complaints related to misclassified rhythms and missed arrhythmia notifications, assisting with investigations and ensuring that all complaints are logged and trends are maintained. You will also assist in the Medical Device Reporting (MDR) process and help maintain compliance with regulatory requirements. Your contributions will be vital in ensuring that iRhythm continues to deliver trusted solutions in cardiac care.

What we offer

At iRhythm, you will be part of a dedicated team that is focused on innovation and improving patient outcomes. We offer a hybrid work environment, allowing you to work from our Deerfield office two days a week while also providing flexibility. You will have the opportunity to grow your skills in a supportive environment that values collaboration and continuous improvement. Join us in our mission to advance cardiac care and make a difference in patients' lives.