Manager, Drug Safety & Pharmacovigilance Operations

At Insmed, every moment and every patient counts — and so does every person who joins in. As a global biopharmaceutical company dedicated to transforming the lives of patients with serious and rare diseases, you’ll be part of a community that prioritizes the human experience, celebrates curiosity, and values every person’s contributions to meaningful progress. That commitment has earned us recognition as Science magazine’s No. 1 Top Employer for five consecutive years, certification as a Great Place to Work® in the U.S., and a place on The Sunday Times Best Places to Work list in the UK. For patients, for each other, and for the future of science, we’re in. Are you? About the Role: You will support the oversight of the Drug Safety and Pharmacovigilance Operations and Vendor Management activities as well as DSPV business partner relationships to ensure compliance with ICH-GCP and GVP guidelines, regulatory requirements, Insmed SOPs, and/or project specific procedures. What You'll Do: In this role, you'll have the opportunity to oversee eTMF management, PV vendor activities and clinical study support for assigned studies to ensure compliance, quality, and alignment with DSPV and regulatory standards. You'll also: Support the oversight of PV Vendor through the development of new Quality Check (QC) activities or maintenance of existing activities, as assigned. Create, track, monitor Key Performance Indicators (KPIs) and metrics for vendor performance monitoring. Identify and address any gaps in vendor case management processes. Serve as the primary liaison and point of contact with internal cross-functional stakeholders (QA, Patient Safety, Compliance, Commercial Strategy) to enhance PV Operational processes to ensure seamless cross-functional integration. Manage correspondence from PV Vendor and PV Related vendors to promptly resolve inquiries related to evaluation and processing of ICSRs. Support the updates of DSPV Operations Controlled Documents. Provide operational support for cross-functional DSPV requests/investigations including those related to Patient Services, QA, PV, Legal, ensuring compliance with PV processes. Enhance DSPV inspection readiness through the development of problem-solving strategies related to ICSR processing, aggregate reports, such as root cause analysis and CAPA development. Facilitate the onboarding, training and mentorship of new hires within the DSPV Operations and Vendor Management Team ensuring they develop a strong understanding of pharmacovigilance processes, regulatory requirements, and vendor oversight best practices to drive operational excellence. Who You Are: You have a minimum of a Bachelor’s degree in one of the life sciences or clinical research and/or a licensed healthcare professional required. You are or have: Minimum of 4-5 years of relevant industry experience which includes at least 3 years of drug safety experience. In-depth knowledge of medical terminology and of GCP, ICH guidelines, global drug safety and drug development process, and current US and international pharmacovigilance regulations. Proven experience handling confidential and sensitive information with the ability to exercise discretion and show good judgment; honesty, integrity, and trust building behaviors in all dealings is essential and required. Strong PC experience and demonstrated proficiency in MS Office (Outlook, Word, Excel, PowerPoint). Demonstrated ability to independently plan and organize own work and effectively manage multiple priorities and responsibilities. Sound judgment in knowing when to escalate issues. Makes sound decisions in absence of Manager. Flexible mindset. Domestic and/or international travel required less than 10% Pay Range: $133,000.00-173,000.00 Annual Life at Insmed At Insmed, you’ll find a culture as human as our mission—intentionally designed for the people behind it. You deserve a workplace that reflects the same care you bring to your work each day, with support for how you wor ... (truncated, view full listing at source)