Job Summary
Serve as a specialist professional in pharmacovigilance within a hybrid work model supporting pharma research and development activities focused on the safe and effective use of medicinal products. Contribute to data driven safety evaluation and collaborate across functions to enhance patient safety outcomes and regulatory compliance.
Responsibilities
Perform end to end case related pharmacovigilance activities that support ongoing pharma research and development and help ensure timely safety reporting to regulatory bodiesReview available clinical and post marketing safety information to identify potential safety signals and contribute to risk assessment activities that protect patientsAnalyze safety data using company systems to detect trends or patterns and escalate relevant findings to medical safety experts for further evaluationDocument all safety case handling steps with clear and accurate narratives that enable transparent audits and inspections by internal and external stakeholdersCollaborate with cross functional research and development teams to integrate safety insights into study design and product lifecycle decisions that advance therapeutic innovationCoordinate with quality and compliance teams to follow current pharmacovigilance procedures and support continuous improvement of standard operating processesSupport preparation of safety sections for regulatory submissions and periodic reports so that product safety profiles are clearly communicated and well justifiedContribute to knowledge sharing sessions with peers to promote consistent case processing practices and strengthen the overall pharmacovigilance capability of the organizationEngage with internal technology and data teams to refine pharmacovigilance tools so that safety data capture and retrieval become more efficient and reliableParticipate in internal audits or readiness activities by providing case related documentation and clarifications that demonstrate strong adherence to pharmacovigilance requirementsAdapt work practices to a hybrid model by using digital collaboration platforms that maintain continuity of pharmacovigilance operations across onsite and remote settingsSupport broader company goals by transforming safety data into meaningful insights that guide responsible use of medicines and create a positive impact on public healthManage personal workload within day shift expectations to ensure all assigned safety activities and timelines are met without the need for travel
Qualifications
Possess a degree in life sciences pharmacy medicine or a related discipline that provides a solid scientific foundation for evaluating drug safety informationDemonstrate two to four years of focused experience in pharma research and development with direct exposure to pharmacovigilance practices and processesApply working knowledge of safety data review tools or databases to manage cases efficiently while maintaining data integrity and traceabilityUtilize familiarity with pharmacovigilance data management concepts to support accurate entry reconciliation and retrieval of safety information when requiredExhibit practical understanding of pharmacovigilance case processing steps including intake coding assessment and follow up activities that align with current regulationsCommunicate clearly in written and spoken form with global stakeholders to ensure that complex safety issues are documented and discussed in an accessible mannerShow commitment to ongoing learning about evolving pharmacovigilance guidelines and research methodologies so professional skills remain current and adaptable
Certifications Required
Desired certification in pharmacovigilance or drug safety such as a recognized pharmacovigilance professional credential
À propos de Cognizant
Cognizant (NASDAQ : CTSH) est un AI Builder et une entreprise de services numériques (ESN) élaborant des solutions complètes d’IA maximisant les investissements pour des résultats concrets. Sa profonde expertise des métiers, des processus et des technologies lui permet d’intégrer dans les systèmes technologiques le contexte unique de chaque organisation de l’ingénierie à la production à l’échelle. Son objectif : améliorer l’efficacité des équipes, créer de la valeur et permettre aux grandes entreprises de rester performantes dans un monde qui évolue rapidement. Pour en savoir plus : cognizant.ai ou @cognizant.
Renseignments suppplémentaires sur l'emploi
Les informations sur la rémunération sont exactes à la date de publication. Cognizant se réserve le droit de modifier ces informations à tout moment, conformément aux lois applicables.
Les exigences linguistiques varient selon les postes, mais nous demandons à tous les candidats d’avoir une connaissance de base de l’anglais afin de faciliter les communications internes à l’échelle de l’entreprise. Pour les postes basés au Québec, une maîtrise de l’anglais est requise puisque vous fournirez des services et collaborerez avec des parties prenantes situées hors de la province, qui ne parlent pas nécessairement le français.
Cognizant est un employeur souscrivant au principe de l’égalité d’accès à l’emploi. Votre candidature et votre dossier ne seront pas examinés en fonction de la race, de la couleur, du sexe, de la religion, des croyances, de l'orientation sexuelle, de l'identité de genre, de l'origine nationale, du handicap, de l'information génétique, de la grossesse, du statut d'ancien combattant ou de toute autre caractéristique protégée telle que décrite par les lois fédérales, provinciales ou locales.
Si vous avez un handicap qui nécessite un aménagement raisonnable pour rechercher une offre d'emploi ou poser une candidature, envoyiez un courriel à [email protected] avec votre demande et vos coordonnées.
