PV Operational Team Lead
__jobinformationwidget.freetext.LocationText__
Shanghai, Shanghai
- Research & Development
- Hybrid
- Full-time
About AbbVie
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.
Responsibilities: Metrics and Oversight of the Pharmacovigilance System • Coordinates the provision of metrics that will ensure oversight of all aspects of the performance and functioning of the PV system in compliance with local regulations, internal company timelines/standards. • For individuals acting as National QPPV / back up National QPPV, as per country attestation form: o Maintains oversight of AbbVie’s PV system master file (PSMF) with the authority to ensure that the information contained is an accurate and up-to-date reflection of the PV system. o Delegates specific tasks under supervision and with documentation, to appropriately qualified and trained individuals, provided that the QPPV maintains system oversight and overview of the safety profiles of all products. Quality Management System • Ensures development and maintenance of local/regional procedures in line with corporate procedures and local requirements. • Ensures the impact assessment of new/updated corporate policies, process, and procedures. • Actively assists with the PV Exception Reporting/CAPA process. • Actively assists with the business continuity plan and testing. • Ensures the development and maintenance of the local PSMF in line with AbbVie’s PV system master file, when required by local/regional regulations. ICSR Management • Ensures ICSR Management process meets all expectations: o Recording, processing, and conducting follow up and translation of adverse events and other safety information from spontaneous and solicited sources. o ICSR expedited reporting according to the local requirements. o local-language medical or scientific literature review. o appropriate local quality control (QC) procedure to ensure quality of information entered and reporting decisions. AE reconciliation and AE identification effectiveness sampling consistent with global procedures. Periodic Safety Reporting • Coordinates the preparation of periodic safety reports (e.g., PSUR)., local annexes, local variations, and translation of safety deliverable documents within the Regional PV team. • Ensures submission of periodic safety reports and ensures documentation of evidence. Audits and Inspection Management • Partners with the Regional PV Lead in managing internal PV audits, audits of affiliate service providers/third parties and Regulatory Authority PV Inspections. • Partners with the Regional PV Lead and coordinates the development of CAPA in response to observations and the tracking actions to completion in a timely manner. Partnership with business partner with possibility for identification and/or handling of safety information • Ensures all PV requirements are in place for activities where there is a reasonable possibility for the identification and/or handling of safety information in accordance with AbbVie procedures and local requirements. PV Training • Ensures overall training compliance and oversight with corporate procedures and local PV requirements, including the maintenance of the PV Training Matrix and the development of additional PV training materials, as required. Legislation Intelligence • Coordinates the monitoring of local (and applicable regional/area) PV-relevant hard intelligence, leading the impact assessment of them. Risk Management • For Individuals supporting Risk Management activities: o Coordinates the receipt and distribution of RMP, Core Implementation Plan (CIP) and additional risk minimization measures (aRMM) to Affiliate stakeholders.. o Develops a deep knowledge of the Risk Management Plans (RMPs) to obtain information on the risk/benefit profile of products. o Liaises with Affiliate stakeholders & Benefit Risk Management (BRM) Team and where applicable, seek involvement of relevant PSEQ stakeholders during development or revision of the COUNTRY Specific Annex (if applicable), Local Implementation Plan (LIP) & local aRMM. o Performs the assessment and implementation of the CIP and accompanying aRMM, when applicable Safety Monitoring For Individuals supporting Safety Monitoring activities Understands and monitors incoming local safety data and communicate changes or potential concerns to the PSEQ Product Safety Team Lead and the EU QPPV (for products marketed in the EEA), for evaluation. o After Hours Availability & Business Continuity ▪ Ensures availability to be at AbbVie’s disposal permanently and continuously on a 24- hour basis, if applicable, and that an after-hours process is in place for the reporting of AEs and that a Disaster Recovery Plan/Business Continuity Plan is established to allow for continuation of critical business processes for PV. Team Lead • Provides strategic and operational leadership to ensure high performing Regional PV systems under their responsibility (coverage up to 3 Affiliates) • Leads recruitment, on-boarding, training, development through coach and mentoring, performance management, and succession planning of appropriately skilled staff (team size up to 8-10 PV Regional staff).
Qualifications: • A minimum of 4-6years experience required within the pharmacovigilance or a related field including experience in overseeing PV operational and compliance metrics • A minimum of 2-3 years people management experience for medium-large sized teams. • Effective communicator and able to work effectively in teams and a cross functional environment • Strong commitment to compliance with relevant rules and procedures • Sound judgement, planning and organizational skills, and the ability to complete activities with high quality. execution of daily tasks and management of responsibilities
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
https://www.abbvie.com/join-us/reasonable-accommodations.html
We have recently become aware of various recruitment phishing scams targeting job seekers. Please be advised:
- AbbVie will never request sensitive personal information (such as bank account details, social security numbers, or payment of any kind) during the recruitment process.
- If you suspect you have received a fraudulent offer or communication claiming to be from AbbVie, please do not respond, open any attachments, or click on any hyperlinks.
If you have any questions or concerns regarding the authenticity of a communication alleged to have been made by or on behalf of AbbVie, please contact us immediately.
Protect yourself by verifying job offers and communications. Your safety is important to us.
Pay Range: $
-
Where We Work
Role is primarily site- or office-based but can occasionally be performed remotely. Employees who are site/office-based and can occasionally perform their role virtually work both in the office and remotely*, following the policies and regulations in place at their location. US Employees must be in the office on Tuesday, Wednesday, and Thursday with flexibility to work remotely on Mondays and Fridays. Three days in the office is the minimum; some individuals or teams may require more in-office days due to meetings, business/project needs or their role.