
Why choose iVigee?
iVigee is a physician-lead pharmacovigilance exclusive company, combining deep regulatory expertise with AI-enabled tools (such as iViReg, iViTracker, iViSight) to support clients' drug safety life cycles.
Founded in 2021, all our leaders have years of experience in all areas of pharmacovigilance - science, regulations, and technology. Our acquisition strategy allows us to attract and choose both the best global talent, and companies.
Our world leading Pharmacovigilance Intelligence platform iViReg is the first to truly focus on the needs of PV professionals, and as we open that system up with our AI interface, we continue to embrace the current and future needs of the pharmacovigilance community and demonstrate our commitment to it.
Our advanced expertise in pharmacovigilance and technology keeps us two steps ahead, delivering sustainable, progressive, and seamless solutions. With strategic centres of excellence in Europe and the US, and our network of experts in over 150 countries, we service the complex global needs of our clients with speed and ease.
We hire for values as much as we hire for expertise. Our culture is built on a shared belief in doing PV the right way, with honesty, ambition, and a genuine care for the work. If these values resonate with you, you'll fit right in.
Fearless
We are not afraid of big tasks and challenges. Not timid to speak up, not timid to ask. Always seek and speak the truth.
Trustworthy professionals
Our competence gives us confidence that we will deliver on our promises. We do it with integrity and quality that earns trust. We do it with a smile, as we love our work that makes our clients happy, saves life and prevents harm.
Enabling innovation
Best practices and tools are giving us our competitive advantage. We are early adopters. We iterate frequently to be better than yesterday, every day.
Sustainable manner
We are interested in long-term relationships, lasting solutions, and good work-life balance. We improve our environment, support communities, raise talent, and build our company to last.
As a company applying the Topgrading methodology, we conduct a thorough recruitment process covering your career history, achievements, challenges, important decisions and key professional relationships. At the final stage, shortlisted candidates will be asked to arrange reference calls with selected former supervisors.
Purpose of the job position:
The Head of QPPV Network and PV Governance is responsible for leading, overseeing, and optimizing the provision of regional Qualified Persons for Pharmacovigilance (QPPVs) and local PV roles (e.g. PV Person at National Level, Person Responsible for Local Literature Screening, or similar), as well as the oversight activities associated with these functions.
This includes ensuring the effective operation of the PV system and its associated Quality Management System (QMS), maintaining the Pharmacovigilance System Master File (PSMF), monitoring the portfolio safety profile, supporting the implementation of risk minimization measures, managing communication with PV stakeholders and Health Authorities, and overseeing overall regulatory compliance. This leadership role ensures harmonized service delivery across the above functions, sustained inspection readiness, and the robust operation of iVigee's pharmacovigilance system. The role is performed remotely from anywhere in Europe.
MAJOR TASKS AND RESPONSIBILITIES:
Leadership of QPPV Office
Functional Strategy, Organisation and Commercial Acumen
Quality and Compliance Oversight
QPPV Network and PV Governance Operations
o Maintaining a compliant PV system, including PSMF management, KPI monitoring, and timely remediation of any identified non-compliance
o Overseeing product safety profiles and emerging safety concerns, including support in risk minimization measures implementation
o Tracking safety commitments and regulatory obligations to ensure ongoing awareness and fulfilment
o Ensuring that all PV information submissions are prepared and filed in accordance with applicable regulations
o Serving as the 24/7 PV contact point for Competent Authorities
o Representing Clients during PV audits and inspections
Vendor Management
Contribution to Business Development
Training and Regulatory Awareness
Collaboration and Representation
Specific requirements for the position:
Education | M.D., Pharmacy, Life Sciences, or equivalent advanced degree |
Experience | Minimum 5 years in pharmacovigilance, with at least 3 years in similar senior compliance function |
Special skills | In-depth knowledge of EU and global/local pharmacovigilance legislation, including GVP Modules I–XV, Proven ability to lead teams and complex quality/compliance systems Active, hands-on use of AI tools in daily work — able to demonstrate concrete examples, including how outputs are verified. |
Language skills | Excellent written and spoken English; confident communicator with regulatory authorities |
Computer skills | Advanced knowledge of Microsoft Office applications |
COS - PV
Remote (Prague, 10, CZ)
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