Regional Safety Officer (Pharmacovigilance) UK & IE

The primary objective of the United Kingdom and Ireland (UK/IE) Regional Safety Officer (RSO) position is to manage the local pharmacovigilance (PV) system within CSL Vifor UK and Ireland, ensuring compliance with applicable PV regulations and guidelines as well as corporate and Global Safety & Pharmacovigilance (GSPV) policies. This position provides expert input on pharmacovigilance-related matters and develops strategy, ensuring PV processes are completed seamlessly in support of the affiliate organization’s long-term vision and goals. This role is strictly non-promotional and operates in alignment with the principles of CSL’s Global Safety Governance System to ensure maintenance of the company’s license to operate. If you are considering sending an application, make sure to hit the apply button below after reading through the entire description. Responsibilities include: – Establishes and maintains local PV systems in compliance with national regulations and GSPV policies. Leverages a diverse and robust set of sources including but not limited to regulatory intelligence, continuous improvement initiatives, key performance indicators (KPIs) as well as audit / inspection findings, to evolve and enhance the local PV system. Ensures comprehensive oversight of all local pharmacovigilance (PV) activities conducted at CSL, and establishes a robust framework for assessing potential risks, monitoring trends, and managing emerging issues. Maintains close liaison with the UK QPPV and IPV Head of Europe. May act as the National contact person/UK QPPV/deputy UK QPPV and fulfil regulatory defined responsibilities in accordance with CSL procedures, as and when required. Provides strategic leadership and guidance to Pharmacovigilance (PV) and Medical Information (MI) team members, as well as the wider organisation, to ensure the delivery of MI and PV activities in alignment with the requisite quality and compliance standards. Directly manages and develops the local PV team, setting clear performance expectations and providing regular feedback. Fosters a collaborative and high-performance culture within the team, encouraging innovation and continuous improvement. Conducts Provides guidance to direct reports on the execution of local PV processes. Defines strategy to ensure PV processes are completed by the team consistently and efficiently with quality and compliance integrated at their foundation. Responsible for the establishment, maintenance, and oversight of local Pharmacovigilance (PV) processes, including but not limited to: Management of Individual Case Safety Reports (ICSRs), encompassing their handling, reporting, and follow-up, as well as compliance oversight where applicable. Reconciliation of ICSRs with relevant internal stakeholders, such as Global Case Management, local Quality, Medical Information and Sales Force, as well as third parties (e.g., distributors, Medical Information vendors, Organised Data Collection Systems (ODCS), service providers, etc.). Regular screening of local literature, ensuring that all identified safety information is managed in accordance with local and global processes. Maintains up to date information relevant for the Pharmacovigilance System Master File (PSMF) or local PSMF as required by local regulations. Oversight of the submission status of aggregate reports (e.g., PSURs) to the relevant regulatory authorities, as well as the preparation or contribution to local aggregate reports, Risk Management Plans (RMPs), and supporting documents where necessary. Implementation of additional risk minimization measures (aRMMs), where applicable. PV oversight of local digital and social media channels. Ensuring the existence and regular testing of a local PV business continuity plan. Documentation of local PV activities in appropriate procedures and records. Storage and archiving of PV-related documents and records in GXP validated repository. Conducting local reportability assessments and the reporting of signals and urgent safety information to local regulatory authorities as required. Acts as a primary point of contact for all PV-related matters in their territory/region, and timely communication and escalation of PV-relevant issues as per established local and global processes. Responsible for ensuring awareness and compliance with current PV regulations and guidelines. Oversees the local assessment, communication, and implementation of new or updated PV requirements, including notifying Global of local reporting obligations to ensure the Global Safety Database remains compliant. Provides strategic advice to management and updates-controlled documents and platforms to align with evolving regulations. Establishes good working relationships with GSPV, Global Regulatory Affairs (GRA) and local functions, such as Local Quality Officer (e.g., for PTCs), Marketing and Medical Affairs (e.g., for ODCSs), Commercial Operations, Research & Development Quality Assurance (R&DQA) and Clinical Maintains up-to-date understanding of safety profiles of registered and investigational products. Supports and collaborates with cross-functional teams to identify and investigate safety concerns, contributing to the evaluation of product safety risks. Partakes in internal meetings regarding product safety as applicable. Develops and presents strategic PV plans and proposals, highlighting their impact on broader affiliate organisation and regulatory compliance. Ensures that PV activities support the affiliate organization’s long-term vision and goals, fostering a proactive approach to risk management and regulatory adherence. Monitors and evaluates the effectiveness of PV strategies, making data-driven recommendations for continuous improvement. Provides expert input on PV-related matters, ensuring that PV activities are integrated into the broader organizational strategy. Facilitate cross-functional collaboration to ensure seamless integration of PV activities with other business functions, such as Marketing, Commercial, and Medical Affairs. Provide regular updates to senior management on PV performance, trends, and emerging issues, ensuring informed decision-making at the highest levels. Lead initiatives to enhance the visibility and understanding of PV within the organization, promoting a culture of safety and compliance. Ensures appropriate pharmacovigilance oversight of all Organized Data Collection Systems (ODCS) within the territory, ensuring adherence to relevant processes. Facilitates the implementation of Pharmacovigilance Agreements (PVAs) in close collaboration with the relevant Global Safety and Pharmacovigilance (GSPV) functions and local teams e.g. Global Pharmacovigilance Agreements and Alliance (GPAA) and International Partner Market (IPM) team. Responsible for the management and oversight of third-party subcontracted activities, maintaining local control and accountability. Conducts reviews of relevant Quality Agreements with business partners, ensuring pharmacovigilance obligations are incorporated into PVAs as needed in collaboration with GPAA. Key PV point of contact for local PV inspection by competent Regulatory Authorities and/or PV affiliate audits in the territory, in collaboration with UK QPPV, GSPV IPV, PVRQA, and relevant local functions. Ensures audit / inspection preparation and close-out activities including the development of a CAPA plan and the close out of any audit / inspection action items. Responsible as the follow up coordinator for CAPAs raised and for the close out of audit action items, where necessary. Manages PV training requirements of affiliate personnel and personnel of relevant 3rd party service providers, ensuring these personnel are aware of their PV reporting obligations. This includes development of training materials with IPV, delivery of regular and ad-hoc training, and monitoring of training compliance. Qualifications Skills and Experience: – Degree in life science, nursing, pharmacy, or other related area; or Equivalent experience Qualifications in line with relevant local legislation 7+ years in the pharma industry, and knowledge in pharmacovigilance; OR Equivalent experience in line with relevant local legislation Ability to work effectively and collaboratively across local affiliate functions the GSPV organization and other CSL functions. Ability to establish and maintain good working relationships with internal and external stakeholders. Excellent verbal and written communication skills in English Fluent in local language(s) of territory if required by legislation. Ability to manage, resolve or escalate issues as appropriate. About CSL Vifor CSL Vifor aims to become the global leader in iron deficiency and nephrology. The company is a partner of choice for pharmaceuticals and innovative patient-focused solutions across iron, dialysis, nephrology and rare conditions. CSL Vifor strives to help patients around the world with severe, chronic and rare diseases lead better, healthier lives. It specializes in strategic global partnering, in-licensing and developing, manufacturing and marketing pharmaceutical products for precision patient care. For more information, please visit viforpharma.com We want CSL to reflect the world around us As a global organization with employees in 35+ countries, CSL embraces diversity and inclusion. Learn more about Diversity & Inclusion at CSL. Do work that matters at CSL Vifor!