China PV Lead

BioSpace; Shanghai (VA); Presencial; USD 120.000 - 180.000; Jornada completa

Descripción de la vacante

AbbVie seeks a Pharmacovigilance leader to oversee the PV system, ensuring alignment with local and regional regulations across affiliates. You will coordinate ICSR processing, safety reporting, and audits, while guiding CAPA execution and safety governance.

The role requires strong English communication, medical or life-sciences background, and at least two years in pharmacovigilance. Collaboration with medical, regulatory and regional teams will be essential for compliant risk management.

Formación

• Medical, pharmacy or life-sciences degree (or equivalent).
• At least two years’ experience working in the pharmaceutical industry in a pharmacovigilance role is required.
• Excellent written and spoken communication and presentation skills.
• Fluency in written and oral English is essential to facilitate communications with PSEQGPS, Area/Regional.

Responsabilidades

• Oversight of the Pharmacovigilance System to ensure compliance with local and regional regulations.
• Maintain oversight of PV activities and performance, including ICSR processing and safety reporting.
• Lead Affiliate PV audits and regulatory inspections and manage CAPA timelines and effectiveness.
• Develop PV training programs and ensure training compliance with corporate and local requirements.
• Monitor safety data and support risk management activities across the product lifecycle.

Conocimientos

Communication skills

English fluency

Educación

Medical, pharmacy or life-sciences degree

Descripción del empleo

Company Description

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.

Job Description

Oversight of the Pharmacovigilance System

Ensures that PV processes, procedures and systems are in place to comply with AbbVie Global PV procedures and with local and/or regional PV regulations.

Maintains oversight of the performance of all activities that fulfil local and applicable regional PV regulations, including those performed by PSEQ the Regional PV Teams and/or outsourced partners, in collaboration with Regional PV Leaders who oversee day-to-day operational PV activities.

(National QPPV / back-up National QPPV only) 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.

Quality Management System

Partners With PSEQ The Regional PV Teams To

Ensure Affiliate PV System procedure(s) aligns with corporate PV procedures and complies with local and regional PV regulations.

Manage any non-conformity and/or planned departures from corporate and/or local PV procedures according to the global issue and exception management process and ensure any corrective/preventive actions are completed according to the schedule.

Maintain oversight of the PV training plan and ensure training compliance of local PV personnel and other affiliate personnel with corporate and local PV training requirements.

Oversee training compliance of partner company staff according to local contract requirements.

Adverse Event & Periodic Safety Reporting

Maintains oversight of the PV system and ensures that processes, procedures and systems are in place for intake, processing, conducting follow up, translation and reconciliation of adverse events and other safety information reportable to PPS GPS from spontaneous and solicited sources as well as from clinical studies.

Partners with the Regional PV Teams in PSEQ GPS to ensure reporting of both clinical and post-marketing Individual Case Safety Reports (ICSRs) and Periodic and Aggregate Reports to the Regulatory Agencies, Ethics Committees and Investigators, in compliance with corporate PV procedures and with local and regional PV regulations as required.

Audits and Inspections

Serves as the Affiliate Lead and point of contact for affiliate PV audits and Regulatory Authority PV inspections, demonstrating understanding of the overall AbbVie PV system and how Global PV processes and PSEQ the GPS Regional PV Teams are set-up and structured, supporting the fulfilment of local legal requirements.

Collaborates with the GPS PSEQ Regional PV Teams in to manage managing audits of processes executed by the Regional PV Teams and as well as audits of affiliate service providers and third parties.

Supports PSEQ Collaborates with GPS Regional PV Teams in the development of CAPA in response to observations and the tracksing actions to completion in a timely manner.

Partnership with business partner with possibility for identification and/or handling of safety information

Acts as key safety advisor for affiliate cross-functional partners on safety topics to address business needs and ensure ensuring that business partnerships involving activities where there is a reasonable possibility for the identification and/or handling of safety information are assessed for the generation of safety information and the applicable PV requirements, and that applicable PV and safety data exchange agreements are implemented.

Partners with PSEQ the GPS Regional PV Teams to ensure that:

All sources of adverse events and other safety information are identified at the local level and mechanisms are in place for collection and collation of all data by PSEQ GPS.

Content of local Safety Data Exchange Agreements (SDEAs) and other PV agreements conforms to AbbVie procedures and local requirements and maintains the inventory in the PPS GPS PV Agreements Database.

Compliance with local agreements.

PV Training

Collaborates with PSEQ the GPS Regional PV Teams to ensure overall training compliance 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

Collaborates with PSEQ the GPS Regional PV Teams to ensure monitoring of local (and applicable regional/area) PV-relevant hard intelligence, and leads leading the impact assessment of such intelligence them.

Risk Management

Leads the Affiliate Risk Management Team (ARMT) local risk management activities in alignment with local regulations with the Affiliate Medical Director (AMD).

Coordinates the receipt and distribution of Risk Management Plans (RMPs), Core Implementation Plan Strategy (CIS CIP) and additional risk minimization measures (aRMM) to relevant affiliate stakeholders ARMT members.

Develops a deep knowledge of the Risk Management Plans (RMPs) to obtain information on the risk/benefit profile of products.

Liaises with ARMT & Benefit Risk Management (BRM) Team the affiliate stakeholders and the Office of Risk Management and where applicable, seek involvement of relevant PSEQ global stakeholders during the development or revision of the local RMP or RMP COUNTRY Specific Annex (if applicable), Local Implementation Plan (LIP) & local or country-specific aRMM.

Performs the assessment and implementation of the CIS and accompanying aRMM, when applicable.

Safety Monitoring and Evidence Generation

Maintains an overview of medicinal product safety profiles and any emerging safety concerns for company products marketed within the relevant jurisdiction, and maintains awareness of conditions or obligations adopted as part of the marketing authorizations, commitments relating to safety or the safe use of the products and of post-authorization safety studies requested by a regulatory agency.

Be a key driver in the generation and interpretation of safety evidence across the product lifecycle.

Understands and monitors incoming local safety data and communicate changes or potential concerns to the PSEQ GPS Product Safety Team Lead and the EU QPPV (for products marketed in the EEA) for evaluation.

Through the oversight of pharmacovigilance processes and the active monitoring of safety data, the ASR ensures that robust evidence is generated to inform risk management, regulatory submissions, and product safety profiles.

Reviews summary reports of local research-related activities and communicates any safety insights/findings with Medical Teams and PSEQ GPS.

Leads product safety communication and education initiatives for local cross-functional teams on major PV topics and on local data sources.

Launch Readiness

Sets a solid local safety and PV strategy incorporating proactive PV contributions to ensure a successful product or indication launch at the affiliate.

Acts as key safety advisor for affiliate cross-functional partners on safety topics.

PV Advocacy

Maintains awareness, oversight and actively contributes to assessing the impact of new legislations on the PV system. Drives AbbVie PV advocacy efforts through strong internal and external collaboration including and engagement with in local trade associations, industry network, and with Regulatory Agencies.

Collaborates on internal and external PV advocacy efforts, in alignment with the AbbVie, PSEQ GPS, and QPPV Office advocacy guidance.

After Hours Availability & Business Continuity

Ensures that a local Affiliate PV Disaster Recovery Plan/Business Continuity Plan is established in a risk-based manner to allow for continuation of critical business processes for PV.

(National QPPV / back-up National QPPV only) 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.

Qualifications

• Medical, pharmacy or life-sciences degree (or equivalent).
• (National QPPV only) (adjust above accordingly to reflect the regulatory requirements for NQPPV)
• At least two years’ experience working in the pharmaceutical industry in a pharmacovigilance role is required.
• (National QPPV only) Adequate theoretical knowledge and practical experience of PV activities and system under purview (as stipulated in local guidance) and sound understanding of the regulatory and PV monitoring requirements for assigned territory(ies) that comply with any specific training requirements mandated by relevant regulatory agencies.
• Excellent written and spoken communication and presentation skills.
• Fluency in written and oral English is essential to facilitate communications with PSEQGPS, Area/Regional

Medical And Other Headquarters Functions.

• Fluency in written and oral local language is a requirement to facilitate communications within the affiliate medical department, and with the National Regulatory Agency.

• High customer orientation.

• Strong commitment to compliance with the relevant rules and procedures, and to scientific quality and integrity.

• Demonstrates strong scientific acumen and the ability to understand and apply scientific concepts effectively.

• Sound judgment, strong planning and organizational skills, and the ability to get things done.

• Demonstrated strong sense of urgency.

Critical Success Factors

• Builds and maintains strong relationships with affiliate stakeholders (e.g. Medical Affairs, Regulatory Affairs, Commercial) and PSEQGPS.
• Learns fast, grasps the “essence”, ability to manage complexity and changes to change course quickly where indicated to add value to the PV system.
• Acts consistently with AbbVie’ s ethics, obligations and local laws – putting patient safety, partnerships and overall AbbVie’s interests before individual, immediate team and functional interests.
• Strengthens the use of product safety knowledge and channels scientific safety evidence and benefit-risk information to area and affiliate stakeholders to positively impact business strategies.

Additional Information

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