-Monitors and audits the company’s drug, biologics or medical devices surveillance program including the intake, evaluation, processing and follow-up on adverse reports. Participates in the resolution of any legal liability and in complying with government regulations. Ensures accurate receipt, maintenance and assessment against product labeling. Reports events or reactions as required by regulatory agencies including adverse events data from clinical trials, spontaneous or solicited sources, periodic and experience reports. May provide trending and safety signal detection and assessment. Supports all clinical trial activity and post marketing.

Key responsibilities:

•To support management of operational processes in ensuring compliance with Novartis global/local procedures, national and international regulations/standards/guidelines for pharmacovigilance of Novartis marketed and investigational products -Manage collection, processing, documentation, reporting and follow-up of all adverse events (AE) reports for all Novartis products from clinical trials, post-marketing studies (PMS), Patient Oriented Programs (POP), registries and all Spontaneous Reports (SR).

•Transcribe, translate (where required) and enter data of all Serious Adverse Events (from Clinical Trials,) and all adverse events (from POPs, PMS, registries and all SRs) from source documents onto safety systems accurately and consistently with emphasis on timeliness and quality.

•Record and track receipts, submissions and distributions of documents like SAEs, SRs, Investigator Notifications etc in cooperation with other departments -Manage reporting/submission/distribution of safety reports/updates/information to Local Health Authorities and/or clinical operations in cooperation with other Departments.

•Work with other local/global PV associates to ensure accurate evaluation of safety data.

•Interact and exchange relevant safety information with LHA, PV associates, other functional groups and third party contractor, if applicable.

•Survey and monitor global/ regional/national (as applicable) pharmacovigilance regulations and provide update to global PVO organization.

•Develop, update and implement local procedures to ensure compliance with PVO global procedures and national requirements.

•Management and maintenance all relevant assigned PVO databases, if applicable.

•Develop and update training materials for pharmacovigilance -Ensure support for and close-out of audits, corrective action plan activities and Health Authority inspections.

•Provide timely, relevant information to trial coordinators, CRAs and other Novartis staff -Distribution of marketing samples (where applicable)

Essential requirements：

•Functional Breadth, collaborating across boundaries, operations management and execution.

•2 years as Patient Safety Specialist (preferred)

​​ Desirable requirements：

•Knowledge of national and international regulations for pharmacovigilance

•Knowledge of pharmacological and medical terminology

•Good communication and interpersonal skills Quality and results oriente Project management skills

为什么选择诺华：帮助患者及家属不仅需要创新科学，还需要一支包括你我他在内的充满智慧与激情的团队，大家相互协作、支持与激励。共同实现突破，改变患者的生活。一起共创更好的未来，你准备好了吗？

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Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together?

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Databases

Safety Science

Pharmacovigilance

Filing Documents

Employee Training

Reporting