Senior Reg Affairs Specialist (Reg Liaison) | H016

Senior Reg Affairs Specialist (Reg Liaison) | H016

11 feb
|
Thermo Fisher Scientific
|
Nuevo Casas Grandes

11 feb

Thermo Fisher Scientific

Nuevo Casas Grandes

.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 are currently seeking a Senior Regulatory Affairs Specialist to join our growing Regulatory Affairs department - Regulatory Liaison team.
This is a fantastic opportunity to further your regulatory career and develop your expertise in this field.
**Senior Regulatory Affairs Specialist - Reg Liaison**In this role you will be a pivotal team member with ideally with regulatory experience.
You will provide innovative solutions including global regulatory therapeutic area expertise and client interface to provide strategic regulatory intelligence, guidance and regulatory expertise for product development from preclinical through registration and product optimization.
You will feel confident providing regulatory advice and carry out projects in the provision of regulatory affairs services whilst acting as liaison with internal and external clients in the provision and marketing of these services.In this role as a Senior Regulatory Affairs Specialist, you will be part of our Regulatory Science Liaison team,



leading on communications with regulatory agencies as part of centralized regulatory submissions including but not limited to the EU CTR process.
You will partner with our Regulatory Affairs leads, in providing regulatory affairs strategy technical/project leadership on a regional/global level

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