Marketed Product Safety Associate Director - Ciudad de México - IQVIA

IQVIA

Empresa verificada

Ciudad de México

hace 3 semanas

Publicado por:

Rodrigo Fernández

Reclutador de talento para beBee

Descripción

Support the development of project objectives, budget, and scope

Develop and maintain project documentation associated with delivery and coordination of local QPPV/national contact for pharmacovigilance activities.
General project management administration activities
Manage notifications to support updates to Regulatory Intelligence Database (RID) (i.e. updates to Health Authority requirements as provided by Local QPs)
Contribute to PSMF (new /updates) for Local QPPV sections
Act as National PSSF Coordinator, if required
Performance monitoring, including oversight of performance of local QPPVs/national contacts against standard work instructions and procedures
Routine status reporting on overall progress, including coordination and management of monthly QPPV/national contact activity reports
Hosting client/local QPPV stakeholder meetings as required by Project
Ongoing assessment of project risk and issue mitigation
Provision of support with routine audits and inspections
KPI monitoring
Escalation point for issues associated with Local QPPV network
Assist in the coordination of projects and resources, ensuring quality deliverables to customers.
May contribute to discussions with clients on project deliverables as appropriate. Ensure staff have a consistent understanding and positive impression of business strategy for regional and global objectives.
May have financial responsibility and accountability for team
Responsible for monitoring growth and performance.
May take a proactive role in developing long standing relationships with IQVIA customers, and may take a leadership role in bid defense strategy and planning, as appropriate.
Improve Local QPPV, and pharmacovigilance agreement procedures and standards. May participate in quality or process improvement initiatives.
Act as primary interface for customers and provide expert input on delivery of Local QPPV services required by assigned customers.
Represent QPPVs and PVA staff on task forces as needed.
Provide advice, support, guidance and training as needed and serve as a mentor to colleagues.
Ability to establish and maintain effective working relationships with coworkers, managers and clients.
Performs other duties as required.

Requirements:

Bachelor's Degree in health science or related area
2 years' clinical research experience in a Contract Research Organization or Pharmaceutical company, including at least 8 years pharmacovigilance experience. Equivalent combination of education, training or experience.
English advanced.
Excellent knowledge of Lifecycle Safety processes.
Excellent attention to detail and accuracy and maintain consistently high quality standards.
Excellent written and verbal communication skills.
Effective mentoring skills.
Ability to work effectively on multiple projects simultaneously.
Organize own workload and effectively time manage competing priorities.
Ability to establish and maintain effective working relationships with coworkers, managers and clients.