Role Overview

The PV Coordinator supports the PV Project Manager in coordinating Lifecycle Safety projects across clinical and post-marketing activities. This role focuses on execution tracking and communication to ensure timely high-quality and compliant project delivery while serving as a key liaison across cross-functional teams and stakeholders.

Key Responsibilities

• Support planning tracking and execution of PV projects including maintenance of timelines trackers and deliverables
• Coordinate communication across internal teams and external stakeholders; prepare meeting agendas minutes and action logs
• Track safety deliverables (e.g. case processing regulatory reporting aggregate reporting) and ensure documentation is complete and audit-ready
• Assist with status reporting including dashboards and periodic project updates
• Support financial activities such as effort tracking invoicing inputs and budget updates
• Identify track and escalate risks or issues supporting timely resolution
• Coordinate internal and client meetings including logistics and preparation of materials
• Ensure adherence to SOPs GVP and regulatory requirements; support audit readiness and CAPA tracking

Qualifications & Experience

Bachelors degree in Life Sciences or related field. 46 years of experience in pharmacovigilance clinical research or project coordination. Basic understanding of PV processes and project management concepts preferred.

Skills & Competencies

• Strong organizational and coordination skills with high attention to detail
• Effective written and verbal communication skills
• Ability to manage multiple priorities in a fast-paced cross-functional environment
• Proactive collaborative and solution-oriented mindset
• Familiarity with regulatory requirements (e.g. GCP ICH) preferred

IQVIA is a leading global provider of clinical research services commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race color religion sex sexual orientation gender identity national origin disability status as a protected veteran or any other status protected by applicable law. is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements misrepresentations or material omissions during the recruitment process will result in immediate disqualification of your application or termination of employment if discovered later in accordance with applicable law. We appreciate your honesty and professionalism.