Arrowhead Pharmaceuticals, Inc. (Nasdaq:  ARWR) is a clinical stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing.

Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.

Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI and San Diego, CA.  Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need. 

The Position

The Manager of Good Clinical Practice (GCP), Clinical Quality Assurance is responsible for managing and maintaining quality assurance activities to ensure compliance with GCP standards. This includes overseeing investigator audit programs, developing and monitoring risk management plans, maintaining procedural documents, and generating metrics for continuous improvement. Additionally, the role involves managing quality events for vendors and internal procedures, such as deviations and CAPAs, while collaborating cross-functionally to uphold clinical trial quality and regulatory compliance.

Responsibilities

Duties and responsibilities will include, but not necessarily be limited to, the following:

Develop and maintain clinical quality study risk plans and maintain updates in the Quality Management System Share with functional QA leads risk plans and updates Collect site metrics for the selection of investigator site audits Implement and update investigator site audit annual plans Participate in program and protocol team meetings as the QA representative Leads and coordinates QA to QA relationship with CROs and collects metrics for review Analyzing and reporting trends in audit findings Facilitate ongoing quality improvement through communication of audit results, CAPAs, and GCP guidance and consultation with clinical teams Issuance, review, tracking, and completion of deviations, SCARs (supplier corrective action requests), and CAPAs Provide support for clinical study programs with GCP compliance, as needed Support health authority inspections Communicate any serious or critical compliance risks noted from these activities to senior management (manage reports of Serious Breaches) Participates and leads in generating, training, evaluating, and executing, as required, Arrowhead Standard Operating Procedures and Work Instructions regarding GCP/GCLP/GxP, industry guidelines (such as International Council of Harmonization-ICH) and global regulations Keep up to date with all related quality legislation and compliance issues Ensure regulations are communicated through the development of corporate policies and procedures Assist in document management and training functions across GxP areas as needed Requires occasional travel to other Arrowhead locations (San Diego, CA; Verona, WI; Pasadena, CA)

Requirements

A minimum of a bachelor's degree in a Science discipline A minimum of 5 years of relevant experience in GCP, investigator site audits, and compliance Experience administering deviation and/or CAPA processes. Experience authoring, reviewing, and managing controlled documents Strong knowledge of GCP and Food & Drug Administration (FDA), European regulations, and ICH guidelines.

Preferred

Professional certification in clinical trial auditing is desirable (Certified Quality Auditor, American Society of Quality-ASQ or Certified Clinical Research Professional, Society of Clinical Research Associates-SoCRA) California pay range $125,000—$145,000 USDCalifornia pay range $125,000—$145,000 USD

Arrowhead provides competitive salaries and an excellent benefit package.   

All applicants must have authorization to work in the US for a company.   

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