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Careers in Italy
DEVELOP YOUR CAREER WITH PPD
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| Research Assistant/Project Assistant |
As a research assistant or project assistant you will provide vital support for clinical research projects. You will have excellent communication and organisational skills and a self-motivated, flexible and professional attitude. You must be able to prioritise and work well within a multi-national team environment and have an in-depth knowledge of Microsoft Word, Excel and preferably PowerPoint.
Project assistants will have a good standard of education and two years administration experience.
Research assistants will have a life science/nursing qualification and at least six months administration experience. The research assistant role will provide the training required to progress and become a clinical research associate. |
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| Regulatory Affairs Manager |
Due to an increase in workload we are looking for a Regulatory Affairs Manager to be based in our office in Milan. You will be responsible for providing timely, accurate regulatory advice on strategy and will manage projects in the provision of regulatory affairs services. This will involve you liaising with internal and external clients in the provision and marketing of these services.
A key aspect of your role will be to take primary Regulatory responsibility for effective interactions with the Authorities to support local/central functions and assigned activities. You will also be expected to build and maintain local, central and external relationships in order to influence the regulatory environment, particularly those within Europe.
You may also be required to supervise other regulatory affairs individuals depending on business need.
You will have experience in a broad range of Regulatory Affairs issues gained within the CRO or Pharmaceutical industry. Extensive knowledge of regulatory applications and procedures, especially those related to clinical trials, along with proven success in agency influencing and negotiation, would be an advantage. |
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