Pharmacovigilance associate, Safety data management

About the Department/Company

Alvotech is a fully integrated specialty biopharmaceutical company focused exclusively ondevelopmentand manufacturing of high-quality biosimilar medicines.

Within Research and Development (R&D) function, the integrated Clinical and Medical Research (iCMR) department develops effective strategies aligned with biosimilar guidelines and health authority requirements to deliver successful clinical studies, and support post marketing-authorization related activities.

iCMRis launching an ambitious and exciting project aimed at modernizing andoptimizingthe departmental operating model. As part of this project, we are recruiting for the following position:

Overview ofJobRole

ThePharmacovigilance(PV)Associatewillbe responsible forallassignedClinical Safetyand post-marketingPVactivities. ThePVAssociatewill be part of the newlydeveloped,leanand efficient,Global Safety Data Management team,reporting to theSafety Data ManagementDirector.The focusof this rolewill be onSafety data management activities forcompanyClinical trialsas well aspost-marketing programs.ThePVAssociatewillalsobe involved indevelopmentof theteam’s processes,and development andlifecycle managementofPVsystems.The PVAssociatewillworkonassignedtasks andactivities andensuringregulatory complianceand compliance with company processes.

Scope and responsibility

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Work on assignedClinical Safetyand post-marketingPVtasks(e.g.ICSR/SAE management,Regulatory submissions,Literature monitoring, Digital platform monitoring, Reconciliations, EV, XEVMPD,etc.)

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InvolvedinSafety systemssetup and lifecycle management (e.g.configuration, validation, system lifecycle management, etc.)

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Involved inmaintainingandoptimizingGlobal Pharmacovigilance processes and ensuringcompliance with international law and regulations (e.g.FDA, EMA, ICH).

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Work cross-functionally with other PV department teams andother teams(e.g.Benefit-Risk management, Clinicaltrialsand Partner Compliance),provideinputsandensureon-timedeliveryand compliance

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Work cross-functionally with other teams and departments in the company(e.g.Quality, Regulatory,IT, CPD,etc.) and externally with PV service providers and Business partners

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Deliver trainings on pharmacovigilance processes and standards to company staff and external parties

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Involved in Audits and Inspections related toSafety Data Managementactivities

Job requirements

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Education:Master’s Degree inpharmaceutical sciences or related fields – medicine, pharmacy, life sciences

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Experience:2+years in Pharmacovigilance/Drug Safetyworking in Safety data managementfunctionswith demonstrablehands onexperienceinclinical trial safetyand post-marketing PV activities

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Expertiseworking inSafety systems (e.g., Argus,ARISg);previousexperience with Veeva Safety Vault is great advantage

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Proventrack recordworkingwith global ProductsandClinical trials

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Previousexperience with biologic and combination products is an advantage

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Detailed knowledge of PV processes, directives,regulationsand international guidelines (21 CFR, ICH, GVP, GCP, CIOMS, etc.)

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Mature self-organizational, time-management and interpersonal skills

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Excellent communication skills,maintainsa positive, result oriented work environment

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Able to work independently, plan, organize and deliver, and feel comfortable in a multicultural team.

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Willingness to travel internationally, asrequired