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Job Description
At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.
We hire the best, develop ourselves and each other,
and recognize the power of being one team. We offer continued career advancement opportunities, award-winning training and benefits focused on the health and wellbeing of our employees.
A Day in the Life:
Fulfills the role of European Union (EU) and/or UK Qualified Person for Pharmacovigilance, or Deputy EU/UK QPPV, for selected clients. Works with management to promote services to potential clients and develops service offerings for both developmental and market authorized compounds.
Essential Functions:
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- Fulfills EU QPPV/Deputy EU QPPV role for selected clients in accordance with EU Directive 2001/83/EC, associated EU regulatory guidance and applicable CRG procedures.
- Contributes to scientific safety services, such as safety writing, signal detection and/or literature surveillance.
- Oversees and supports the activities of contact persons at a national level, when applicable.
- Promotes go
📌 Qualified Person (Romano di Lombardia)
🏢 Thermofisher Scientific
📍 Romano di Lombardia
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