Director, Clinical Quality Assurance (GCP)

<div class="content-intro"><p><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Eikon Therapeutics is a new biopharmaceutical company employing revolutionary technology at the intersection of chemistry, engineering, computation, and biology to discover novel treatments for life-threatening diseases. Eikon’s discovery platform is built on groundbreaking innovations from its founders (Nobel Prize, 2014), culminating in the creation of microscopes which enable real time, molecular-resolution measurements of protein movement in living cells, thereby unlocking otherwise intractable classes of proteins as drug targets.</span></p></div><p><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;"><strong>Position &nbsp;</strong></span></p> <p><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">We are seeking an experienced and dynamic Director, Auditor, Clinical Quality Assurance to&nbsp;lead our GCP auditing efforts. The successful candidate will play a pivotal role in ensuring that&nbsp;our clinical trials adhere to Good Clinical Practice (GCP) guidelines and maintain the&nbsp; highest standards of quality. This includes internal audits, site audits, and vendor audits. &nbsp;&nbsp;</span></p> <p><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">This role requires a minimum of 3 days per week onsite (or more, as business needs require) in either our Jersey City (NJ), or Millbrae (CA) offices.</span></p> <p><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;"><strong>About You &nbsp;</strong></span></p> <p><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">You are an expert-level auditor with the discipline and consistent follow-through to see complex&nbsp;audit programs through to completion. You are an excellent communicator who builds trust and collaborates effectively with stakeholders. You thrive as part of a dynamic team, and you're&nbsp;motivated by the opportunity to drive projects and results while mentoring and developing&nbsp;others. &nbsp;</span></p> <p><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;"><strong>What You’ll Do &nbsp;</strong></span></p> <ul> <li style="font-family: arial, helvetica, sans-serif; font-size: 12pt;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Lead and manage the Clinical Quality Assurance (CQA) audit program, ensuring&nbsp;compliance with GCP, applicable regulations, and company SOPs. &nbsp;</span></li> <li style="font-family: a