Head of Global Pharmacovigilance Center of Excellence
2 weeks ago
Team: R&D, Pharmacovigilance & Regulatory Affairs
Job Type: Direct Employee
Contract Type: Permanent
Location: Parma, IT
About us
Based in Parma, Italy, Chiesi is an international research-focused pharmaceutical and healthcare group with over 85 years’ experience, operating in 31 countries with more than 7,000 employees (Chiesi Group). To achieve its mission of improving people’s quality of life by acting responsibly towards society and the environment, the Group researches, develops and markets innovative drugs in its main therapeutic areas.
We are proud to be the largest global pharmaceutical group to be awarded B Corp Certification, a recognition of high social and environmental standards. p>
We believe that the success of Chiesi is built and shaped by our people and our strong set of shared Values and Behaviors. p>
In fact, we are a global family made up of different cultures, different genders, generations, ethnicities, abilities, sexual identities and many other enriching diversities.
Chiesi Research & Development
Our R&D team represents a fundamental asset for the business. It is divided into integrated functional areas focusing on pipeline projects including discovery and preclinical research, global technical development, drug delivery technology, clinical development, regulatory affairs, pharmacovigilance, intellectual property, quality assurance, R&D project and portfolio management.
Purpose• To design, drive, and oversee cross-functional projects within GPV and between functions aiming at increasing the value that GPV can bring to the Chiesi business.
• To oversee signal and risk management activities for Chiesi products to ensure patient safety and compliance with global regulatory and quality standards.
• To oversee and maintain robust procedures for the planning, preparation, and submission of high-quality aggregate safety reports, in compliance with requisite global and local regulations and requirements./>• Manage the CoE team including the distribution of assignments, prioritization of tasks, personal objectives, and mentorship/training as required.
• Act as safety lead for the overall benefit-risk strategy of the Chiesi product portfolio.
• To provide input to the safety signal management, input to safety-related global labelling changes, and safety-related contributions to responses to regulatory authority.
• To manage the CoE budget for projects, activities, and people development.
Experience Required
Minimum 5 years of experience in pharmacovigilance, with theoretical and practical knowledge of Pharmacovigilance at both global and local scales.
EducationMaster's degree in science, PhD or similar preferred.
LanguagesSoft Skills- Conflict management
- Leadership and social influence
- Analytical skills
- Planning and organizational skills
- Strategic thinking
What we offer
You would join a dynamic, fast-growing, challenging, and friendly environment.
In Chiesi we firmly believe that our people are our most valuable asset, that is why we invest in continuous training, learning, and development. Therefore, we strive to continuously promote and satisfy development needs, paying particular attention to the quality of our working environment and to collective well-being.
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