The primary objective of the Saudi Arabia Local Safety Officer (SO) position is to manage the local pharmacovigilance (PV) system(s) in CSL Vifor ensuring compliance with applicable Saudi Arabia PV regulations and guidelines as well as corporate and Global Safety & Pharmacovigilance (GSPV) policies. Serve as a deputy, covering PV responsibilities for the Middle East Turkey & Africa (META) region as needed.

In this position you will be directly reporting to the International Partner Markets Senior Manager (META)

Key Tasks

Establishes and maintains Saudi Arabia PV systems in compliance with Saudi FDA 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 Saudi Arabia 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.

Responsible for the establishment, maintenance, and oversight of Saudi Arabia 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 PSSF as required by local Saudi 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.Conducting local reportability assessments and the reporting of signals and urgent safety information to local regulatory authorities as required:

Conducting signal detection based on local safety data.

Ensure timely reporting of validated signals by global team to SFDA using the most updated template for the cover letter per Saudi GVP.

Collaborate on corrective actions as required.

Exchanging of all signal (local and global with global team on monthly basis and update global team of all submissions to SFDA details.

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.

Providing guidance to direct reports on the execution of local PV processes.

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 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.

Participates in local Commercial Operations Leadership Team meetings as required and provides input to strategic planning discussions as needed, ensuring alignment of PV activities with broader organizational objectives.

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 CSL 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.

Your Profile

Degree in life science, nursing, pharmacy, or other related area; OR

Equivalent experience in line with relevant local legislation 

Qualification in line with relevant local legislation

3+ years in the pharma industry, and knowledge in pharmacovigilance; OR

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 

Good verbal and written communication skills in English 

Fluent in local language(s) of territory

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

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