regulatory affairs specialist in siena

job type
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job details

siena, toscana
job category
Infermieristica, farmacia, medicina
job type
working hours
Full Time
1 anno
reference number
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job description

For major multinational pharmaceutical company we are looking for a Regulatory Affairs Specialist.
Lingua: Inglese


Requirements: -Scientific degree is preferable + 3 or 4 years specific RA experience -Excellent knowledge of written and spoken English -4 years work experience with Pharmaceutical Regulatory Affairs. - Knowledge of regulatory procedures and requirements. - Working knowledge of electronic tools/systems. - Ability to work in an autonomous manner and manage his/her time. - Good communication skills and culturally aware


Main activities: - Coordinate and having responsibility for the preparation of regulatory submissions such as clinical trials applications, IND submissions and amendments,variations, renewals, support for marketing applications (International/LatAm) etc. (under the general guidance of their supervisor). - Participate in the approval of promotional material as required and helping to resolve external medical/technical enquiries, when required (under the general guidance of their supervisor). - Help develop and review product label texts - Sit on designated working teams and providing regulatory input to these teams including preparation of draft position papers on regulatory issues, draft regulatory sections of project plans and to develop regulatory strategies (to be approved by their supervisor). - Aid in the maintenance of the departmental archive of administrative and technical documentation according to internal procedure. - Provide regulatory advice within the framework of the company’s Change Control procedure, and to support the company’s regulatory compliance personnel (to be approved by their supervisor, as relevant.

educational requirements

Laurea specialistica o a ciclo unico