Perceive Biotherapeutics is an exciting clinical-stage company (lead program in Phase 2), focused

on improving human health by developing breakthrough neuroprotective therapeutics in

ophthalmology that use novel approaches to treat highly prevalent, blinding diseases that

currently have no good therapeutic alternatives. Perceive brings together an experienced, worldclass

team of leaders, scientists and drug developers. Our unique approach is a first-in-class and

best-in-class gene therapy that will significantly impact patients’ lives. Our team is mission driven,

expert, agile and pragmatic.

We are looking for a talented and experienced individual to join our growing Clinical Operations

team and contribute to the company’s long-term goals and success. The successful candidate will

be diversely experienced, thoughtful, collaborative, highly motivated & productive, and possess

the desire to learn, improve processes, and support key clinical stakeholders during our Ph 1 and

Ph 2 trials with an emphasis towards quality, efficiency and operational best practices.

About Us:
Perceive Biotherapeutics (www.perceivebio.com) is an exciting early-stage company, funded by Deerfield Management, with a team focused on improving human health by developing breakthrough neuroprotective therapeutics. We are using novel approaches to treat highly prevalent, blinding diseases that currently have no good therapeutic alternatives. Our unique approach is leading to first-in-class and best-in-class small molecule and gene therapy solutions that will significantly impact patients’ lives.

Position Summary:
The Quality Systems Specialist will play a key role in ensuring the effectiveness and compliance of our Quality Management System (QMS). This position is ideal for a self-driven professional who thrives in a fast-paced, start-up environment and is passionate about contributing to the development of life-saving products. The role requires collaboration across multiple departments to maintain and improve quality systems in alignment with regulatory requirements (FDA, EMA, ICH, etc.) and industry standards.