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Senior Director, Global Pharmacovigilance & Risk Management Head Of Medical Safety

Senior Director, Global Pharmacovigilance & Risk Management Head Of Medical Safety
Company:

Vir Biotechnology, Inc.


Details of the offer

THE OPPORTUNITYVir Biotechnology is seeking an experienced Senior Director to be the Head of our Medical Safety function. Within Vir's Global Pharmacovigilance & Risk Management (PVRM) department, you will provide medical expertise and strategic direction while overseeing the medical safety team, including responsibility for signal management, risk management, and monitoring the safety profile of Vir products. You will shape the strategy and implement pharmacovigilance and risk management activities throughout the product lifecycle (from First-In-Human through post-marketing), assessing benefit-risk profiles, and ensuring corporate compliance with all applicable US and foreign legal and regulatory requirements for signal detection, evaluation, and risk management of Vir products. You will seek to optimize and implement approaches to support the scientific evaluation of the safety risk profile of Vir products.  You will collaborate cross-functionally with colleagues in Clinical Research & Development, Clinical Operations, Clinical Pharmacology, Biometrics, Regulatory Affairs, Medical Affairs, non-clinical safety, QA, and Legal teams.This Senior Director, Global PVRM Medical Safety will perform as a hands-on team leader who is collaborative, a self-starter, and able to work in a matrixed environment. You will report to the Vice President, Global Pharmacovigilance & Risk Management.This is a remote position. Vir only supports employees within the United States and reserves the right to approve work locations.WHAT YOU'LL DODevelop talent and provide leadership to Global PVRM Medical Safety teamProvide strategic planning, implementation, and management of Global PVRM Medical Safety activitiesProvide expert guidance and leadership both internally and externally based on in-depth knowledge of development and post-marketing global regulationsSupport inspection readiness and provide expertise in audits, inspections, and CAPAsResponsible for development of Global PVRM Medical Safety related procedural documentsRepresent Global PVRM Medical Safety as a leader on project teams and committeesLead Safety Review Management Team to address any safety-related issues for Vir products, including safety monitoring in clinical trials, safety assessment for potential signals/risks, responses to Health Authority requests, strategic guidance during NDA/BLA submissions, and creating and maintaining core safety information in Investigator Brochures, Company Core Data Sheets, and local labels for Vir productsContribute to safety related sections of clinical study documents (e.g., Study Protocols, Informed Consent Forms, Statistical Analysis Plans, Clinical Study Reports, IB Reference Safety Information, Summary of Clinical Safety, Integrated Clinical Safety, Publications, Manuscripts)Perform medical review of Individual Case Safety ReportsPerform medical review and analysis for aggregate safety reports and responses to ad-hoc requests for safety informationProvide leadership in regulatory authority interactions regarding safety and risk managementLead the negotiation of safety data exchange/pharmacovigilance agreements with license partners and distributors for drug safety and risk management related activitiesWHO YOU ARE AND WHAT YOU BRINGMedical degree (MD/DO), PharmD, or equivalent required, with at least 2 years of experience in clinical/medical practice13+ years of related experience with 8+ years leading Safety TeamsExperience in authoring safety signal assessment reports, DSUR, PBRER, RMP, and RSIExperience with signal detection process and managing safety information from clinical development and post-marketing sourcesExperience with Global regulations and ICH guidance governing pharmacovigilance and risk managementKnowledge of drug development process, pharmacovigilance databases, and MedDRA codingProven record as a people leader in a remote environment maximizing team cohesion, performance, and efficacyWHO WE ARE AND WHAT WE OFFERThe expected salary range for this position is $225,500.00 to $329,500.00. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors.Vir's compensation and benefits are aligned with the current market and commensurate with the person's experience and qualifications. All full-time employees receive a package that includes: compensation, bonus and equity as well as many other Vir benefits and perks such as: health, dental, vision, life and disability insurance benefits, non-accrual paid time off, company shut down for holidays, commuter benefits, child care reimbursement, education reimbursement, 401K match and lunch for all onsite employees!#LI-225024411_AA1#LI-Remote


Source: Greenhouse

Requirements

Senior Director, Global Pharmacovigilance & Risk Management Head Of Medical Safety
Company:

Vir Biotechnology, Inc.


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