Job Details
Title:
Associate Director, GCP Quality Assurance
Location:
La Jolla, California
Company Overview
Avidity Biosciences is pioneering a new class of oligonucleotide-based therapies called AOCs designed to overcome the current limitations of oligonucleotide therapies in order to treat a wide range of serious diseases. We utilize our proprietary AOC platform to design, engineer and develop therapeutics that combine the tissue selectivity of monoclonal antibodies (mAbs) and the precision of oligonucleotide-based therapies in order to access previously undruggable tissue and cell types and more effectively target underlying genetic drivers of diseases. We are passionate about the impact of every employee in bringing these potentially transformative therapeutics to patients in need. Make a difference with us.
Position OverviewThe Associate Director, GCP Quality Assurance, reporting to the Director of Quality Assurance, will manage the clinical quality function by supporting and providing oversight of clinical trials and clinical activities, establish and manage clinical quality systems, and ensure GCP compliance. The candidate will be hands-on and actively involved in executing GCP QA strategy, and support GCP compliance and alliance activities with vendors and business partners. The personnel will collaborate cross-functionally with various departments within the organization, and ensure effective communication and constructive working relationships with colleagues and business partners to enable global development of Avidity therapeutics.Responsibilities
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