Assistant/Associate Director, Pharmacovigilance Quality Assurance

Headquartered in Carlsbad, California, and with offices in Boston, Massachusetts, and Dublin, Ireland, Ionis has been at work for more than three decades discovering medical breakthroughs that have redefined life for people with serious diseases. We’re pioneers in RNA-targeted medicines, and our platform continues to revolutionize drug discovery and transform lives for patients with unmet needs. With multiple marketed medicines and a leading pipeline in neurology, cardiology and select areas of high patient needs, we continue to drive innovation in RNA therapies in addition to advancing new approaches in gene editing to provide greater value to patients and are well positioned financially to deliver on our strategic goals.

At Ionis, we pride ourselves on cultivating a challenging, motivating and rewarding environment that fosters innovation and scientific excellence. We know that our success is a direct result of the exceptional talents and dedication of our employees.

With an unprecedented opportunity to change the course of human health, we look to add diverse individuals, skill sets and perspectives to our exceptional team. We continue to invest time, money and energy into making our onsite, hybrid and remote work environments a place where solid and lasting relationships are built and where our culture and employees can thrive.

We’re building on our rich history, and we believe our greatest achievements are ahead of us. If you’re passionate about the opportunity to have meaningful impact on patients in need, we invite you to apply and join us. Experience and contribute to our unique culture while you develop and expand your career!

ASSISTANT/ASSOCIATE DIRECTOR, PHARMACOVIGILANCE QA Summary We are seeking a highly motivated individual to join as an Assistant/Associate Director, Pharmacovigilance Quality Assurance. This is a hands-on QA role within Development Quality Assurance that supports the execution of a risk-based GVP quality program. This role partners closely with Patient Safety and Pharmacovigilance, Clinical Operations, Clinical Development, Regulatory Affairs, Medical Affairs, GMP QA, business partners, and service providers to support audit execution, inspection readiness, PV quality systems support, service provider oversight, metrics, and continuous improvement activities, in alignment with Ionis PV QA expectations.

WORK LOCATION remote US-based; at least 10-15% travel

Core Responsibilities GVP Audit Program

• Support implementation and maintenance of a comprehensive, risk-based GVP-compliant quality program covering clinical trial safety and post-marketed safety processes.
• Plan, conduct, and/or support end-to-end GVP audits of service providers, business partners, affiliates, and internal PV processes, including audit preparation, execution, reporting, CAPA follow-up, and closure.
• Prepare and/or review timely, well-written audit reports and communicate findings to auditees, cross-functional representatives, and management.
• Assess and review audit responses to ensure CAPA plans adequately address findings and root causes, including effectiveness checks where appropriate, and maintain, track, and follow up on CAPAs through completion.
• Develop, review, and/or revise audit plans, SOPs, guidance documents, templates, and related documents supporting PV QA activities.

Audit and Inspection Readiness

• Support PV inspection readiness activities and participate in regulatory authority inspections, partner audits, and other external assessments impacting PV systems and processes.
• Lead and/or contribute to the assessment of Health Authority inspection and PV partner audit reports and results, including associated risks and recommendations, for communication to relevant leadership.
• Provide PV QA guidance and training to internal stakeholders involved in clinical development, patient safety, and other applicable functions involved in PV audit and inspection activities, including clinical trial safety processes and GCP/GVP interfaces
• Monitor relevant GVP regulatory intelligence and support assessment and implementation of new or revised requirements affecting clinical trial safety processes, systems, and service providers.

Functional Quality Support

• Provide quality support to Patient Safety and Pharmacovigilance, Clinical Development, Clinical Operations, Regulatory Affairs, Medical Affairs, and other applicable functions on PV an…