GLOBAL PHARMACOVIGILANCE QPPV OFFICE SPECIALIST - TEMPORARY

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 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.
Discover more here We are proud to be the largest global pharmaceutical group to be awarded B Corp Certification, a recognition of high social and environmental standards.
We are a reliable company that adopts and promotes a transparent and ethical behavior at all levels.
We believe that the success of Chiesi is built and shaped by our people and our strong set of shared Values and Behaviors.
Our people make a critical difference to our success, which is why it is vital that we attract and retain the right talent who will continue to enrich our culture by living and breathing our values and behaviors.
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.
Headquartered in the new purpose-built and fully integrated Research and Development Centre in Parma (Italy), the team also has important operations in Paris (France), Chippenham (UK), Cary (US), Stockholm (Sweden), Toronto (Canada) and Shanghai (China).
Who we are looking for Purpose Responsible for maintaining the Global PV System & Standards.
Main Responsibilities To ensure that legal claims are correctly evaluated from a PV point of view and duly reconciled; To ensure the PV Intelligence process across Chiesi's portfolio plus web-screening for Local and global legal requirements (e.
.
HA websites) in collaboration with internal and external  stakeholders is place and performed; To guarantee the PV management in Company sponsored controlled websites/Apps and other social media at corporate and local level.
Experience Required 1 year of work experience in global pharmaceutical companies Education Master Degree in life sciences, pharmacy or related fields  Languages English (fluent) Technical Skills Training and meetings organisation; Basic knowledge of drug development process in a pharma industry; Excellent communication and analytical skills.
Effective communication, interpersonal and decision making skills; Proven ability to manage details, solve problems and keep multiple tasks/ projects on track; Ability to organize and prioritize tasks both; individually and across team to achieve established deadlines; Expertise in scheduling and organizing activities Soft Skills Proactiveness Planning and organizational skills Adaptability and flexibility Goal orientation Time management 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.
We want our people to come to work happy every day, and we know how important it is to find the right work-life balance in order to be able to give our best.
That is why we offer flexible working approach, remote working, support in the relocation process, tax assistance service for foreign colleagues and many other people-care services.