Clinical Document Control Specialist

Embark on an enriching journey with PROCEPT BioRobotics, where our vision, mission, and values guide everything we do as a company. We are committed to revolutionizing treatment for benign prostatic hyperplasia (BPH, otherwise known as prostate gland enlargement) through innovation in surgical robotics. As our company succeeds and grows, we improve the quality of life of patients, provide more effective treatment options for surgeons, uphold the trust of our shareholders. That starts with a commitment to our People with a focus on creating an evolving landscape for your career, brimming with transformative opportunities that provide continuous career growth opportunities.

The Clinical Document Control Specialist is responsible for managing, organizing, and maintaining clinical documentation to ensure compliance with regulatory requirements and internal quality standards. This role supports clinical research teams by overseeing document lifecycle processes, facilitating audits, and ensuring proper archiving and retrieval of essential documents related to clinical trials and post-market studies. This role reports into the Senior Director of Clinical Affairs.