Assoc Mgr, Safety Operations

hace 2 semanas

Xico, México Iqvia A tiempo completo

Job OverviewThe Associate Manager, Safety Operations Team is responsible for leading and overseeing all local pharmacovigilance activities, ensuring compliance with regulations and best practices.This includes the implementation, management, and maintenance of the local pharmacovigilance system.Key ResponsibilitiesOversight of Pharmacovigilance Operations: Monitor and oversee all safety-related operations and communication activities.Serve as the primary point of contact for the Sponsor (when applicable).Ensure efficient and accurate ICSR surveillance, including collection, reporting, and follow-up.Manage translation processes as needed.Author local case narratives for regulatory reporting as required by local authorities.Support local literature searches, reconciliations, and quality assurance activities.Assist with audit and inspection readiness.Collaborate effectively with internal and external stakeholders.Mailbox Screening: Monitor multiple regional/global AE email inboxes in various languages for all Customer Affiliates, assess and take action on all received emails.Case Intake: Create Case Reports in the Global Safety Database.Follow-up Correspondence: Perform follow-up with ICSR reporters to obtain additional information as per SOPs.Reconciliation: Conduct reconciliations with internal functions and licensing partners.Compliance Investigations: Perform compliance investigations for specific cases.QualificationsEducation: Bachelor's degree in Life Sciences.Languages: English (advanced, C1/C2 mandatory); Portuguese (advanced, C1/C2 mandatory).Experience: Minimum 5 years relevant experience, with at least 3 years specific pharmacovigilance experience (intake, case processing, regulatory submissions).SkillsStrong understanding of global and local pharmacovigilance regulations and guidelines.Excellent written and verbal communication skills.Strong organizational and time management skills.Ability to work independently and as part of a team.Proficiency in using electronic data management systems (e.G., Argus, Apex).Preferred QualificationsExperience working with global safety databases.Experience as people manager with direct reports (1 year).Experience in Adverse Events Case Triage, Processing, and Submission.100% home-based role.IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.#J-*****-Ljbffr

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