Student Veterans of America Jobs

Reference #: 396224 Site Name: USA - Pennsylvania - Philadelphia Posted Date: May 10 2024

The Director, US & Regions Intelligence Oversight, Pharmacovigilance (PV) Operations serves as the first point of contact for PV Regulatory intelligence (PVRI), issues and escalations across US & Regional PV Operations, Global Safety (183 country remit). The role will include liaising with our partners in regulatory affairs, medical affairs and clinical operations. The incumbent is a PV exert with deep demonstrated proficiencies in worldwide pharmacovigilance regulations (e.g. US, Canada, EU, UK, Latam, Asia Pacific, Middle East and Africa) necessary to address PVRI & escalations.  Furthermore, this position serves as a strategic partner managing issue, quality and regulatory compliance related to Good Pharmacovigilance Practices (GVP) and holds a regional PV leadership role as it relates to ensuring PV quality of process, tools and technologies in sync with regulatory demand and dynamics.

Key Responsibilities: This role will provide YOU the opportunity to lead key activities to progress YOUR career, these responsibilities include some of the following.

•  The Director, US & Regions Regulatory Intelligence Oversight, PV Operations position is directly responsible for all aspects of day-to-day Regional PVRI, issue management, communication and escalation, CAPA resolution, documentation and timely communication to stakeholders and health authorities as appropriate.
•  Act as Regional gatekeeper and reviewer of all outbound correspondence to health authorities worldwide related to day-to-day PV operations and regions for US FDA, European Union, Emerging Markets and Greater China & Intercontinental (e.g. DHCPL, inspection responses, etc.).
•  Facilitates and maintains PVRI activities worldwide including collection, tracking, assessment and implementation worldwide.
•  Is the PVRI accountable subject matter expert for process and technical workflows in Veeva.
•  Provides high level management and supervision of the company's US and Regional PVRI processes, identifies process gaps and facilitates resolutions congruent with industry best practices.
•  Advises senior management on global safety related strategy and pathways to achieve best in class PVRI operations both in and above country (incl. structure, PV issue and escalation remediations, HA interactions, etc.).
•  Actively develop and manage relevant Regional PVRI SOPs, working practices and guidance to support the Regional delivery as required and incompliance with US and Worldwide regulations.
•  Produce and deliver performance metrics required for oversight of US & Regions PVRI drawing on deep understanding of global safety regulations and health authority expectations.

•  Leverages data and technology to orchestrate safety innovations that deliver against set objectives, defined budgets and timelines (e.g. regional workflow management system(s) life-cycle management, Veeva Vaults, etc.) to ensure oversight of US & Regions.

•  Leads and orchestrates cross-functional US & Regional safety meetings and activities to deliver harmonized issue management for PV

•  Drives centralized/local innovations with ability to scale up throughout the Regional PV Ops remit while ensuring the assigned work complies with GSK established practices, policies and processes and any regulatory or other requirements.
•  Champions safety PVRI management, quality & compliance campaigns and plans to structure in-sync global harmonization of operative processes and procedures.
•  Partner as Deputy to Head of US & Regions PV Operations, with senior local/regional and global roles outside the PV organization and membership at Regional Lead team forums and governance boards to develop strategies to reduce risk to the PVRI system.
•  Escalate non-compliance in the region to Local Risk Board, Head of Regions, Head of Pharmacovigilance (PV Operations), EEA QPPV and Head of Safety as appropriate
•  Plays a leadership role on PV and regional cross-functional teams, including leadership on special projects, participation in continuous improvement and optimization initiatives and PV Ops functional area support in PV audits and inspections.
•  Orchestrates tactful fiscal approaches to PV Regions approach to operations, corporate strategy and commercial business necessary to drive innovation while balancing the dynamic regulatory environment.

Why you? Basic Qualifications: We are looking for professionals with these required skills to achieve our goals:

Advanced degree (MS, PhD, PharmD.) in pharmacy, toxicology, life sciences, or equivalent

10+ years Pharmacovigilance experience

Recent work experience in Veeva Vault

Experience working with regulatory agencies and knowledge of ICH and GCP regulations

Experience leading clinical and global programs

Experience in project management and leading multinational, cross functional teams across a broad spectrum pf PV or related programs, projects or other activities

Experience in people leadership, employee engagement, development and retention either with direct reports or through matrix leadership responsibilities.

Preferred Qualifications: If you have the following characteristics, it would be a plus:

Line management (direct reports) experience is strongly preferred

Strong track record of cultivating and maintaining strategic relationships and collaborations both internally and eternally

Skilled at working effectively with cross functional teams in a matrix organization

Excellent written and verbal communication skills

High degree of problem solving and impact assessment capabilities

Skilled at resolving non-routine issues

#LI-GSK

The annual base salary for new hires in this position ranges from $175,100 to $236,900 taking into account a number of factors including work location, the candidate's skills, experience, education level and the market rate for the role. In addition, this position offers an annual bonus and eligibility to participate in our share based long term incentive program which is dependent on the level of the role. Available benefits include health care and other insurance benefits (for employee and family), retirement benefits, paid holidays, vacation, and paid caregiver/parental and medical leave. Please visit  to learn more about the comprehensive benefits program GSK offers US employees.

Why GSK? Uniting science, technology and talent to get ahead of disease together.

GSK is a global biopharma company with a special purpose - to unite science, technology and talent to get ahead of disease together - so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns - as an organisation where people can thrive. We prevent and treat disease with vaccines, specialty and general medicines. We focus on the science of the immune system and the use of new platform and data technologies, investing in four core therapeutic areas (infectious diseases, HIV, respiratory/ immunology and oncology).

Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it's also about making GSK a place where people can thrive. We want GSK to be a place where people feel inspired, encouraged and challenged to be the best they can be. A place where they can be themselves - feeling welcome, valued, and included. Where they can keep growing and look aft