Regulatory Affairs Officer

Tasks and Responsibilities:Prepares the strategy, the technical documentation, performs the submission (through national and EU portals) and follow-up until approval of MRP, DCP, CP and National Procedures for new marketing authorizations, variations, marketing authorization transfers and renewals according to the relevant EU Regulation and national...

Tasks and Responsibilities: Prepares the strategy, the technical documentation, performs the submission (through national and EU portals) and follow-up until approval of MRP, DCP, CP and National Procedures for new marketing authorizations, variations, marketing authorization transfers and renewals according to the relevant EU Regulation and national...

**Tasks and Responsibilities**: Prepares the strategy, the technical documentation, performs the submission (through national and EU portals) and follow-up until approval of MRP, DCP, CP and National Procedures for new marketing authorizations, variations, marketing authorization transfers and renewals according to the relevant EU Regulation and national...

Tasks and Responsibilities: Prepares the strategy, the technical documentation, performs the submission (through national and EU portals) and follow-up until approval of MRP, DCP, CP and National Procedures for new marketing authorizations, variations, marketing authorization transfers and renewals according to the relevant EU Regulation and national...

**Tasks and Responsibilities**:Prepares the strategy, the technical documentation, performs the submission (through national and EU portals) and follow-up until approval of MRP, DCP, CP and National Procedures for new marketing authorizations, variations, marketing authorization transfers and renewals according to the relevant EU Regulation and national...

Biopharmed: Life Sciences Recruiting **Posizione**: **Biopharmed **is the **head hunting **agency designed to search and select technical and specialized profiles from the **Life Sciences **world. Position: We are looking for a** Regulatory Affairs Manager **for an important service company operating in the regulatory field. **Main responsibilities**: -...

translator Afrikaans Albanian - shqipe Arabic - ‎‫العربية‬‎ Armenian - Հայերէն Azerbaijani - azərbaycanca Basque - euskara Belarusian - беларуская Bengali - বাংলা Bulgarian - български Catalan - català Chinese - 中文(简体中文) Chinese - 中文 (繁體中文) Croatian - hrvatski Czech -...

translatorAfrikaansAlbanian - shqipeArabic - ???????????Armenian - ???????Azerbaijani - az?rbaycancaBasque - euskaraBelarusian - ??????????Bengali - ?????Bulgarian - ?????????Catalan - catalàChinese - ??(????)Chinese - ?? (????)Croatian - hrvatskiCzech - ceštinaDanish - danskDutch - NederlandsEnglishEsperanto - esperantoEstonian - eestiFilipinoFinnish -...

What will you deal with:Manage promotional materials: ensure that all promotional contents and initiatives for pharmaceutical products complies with regulatory requirements and industry standards, overseeing the approval process before materials are used in marketing campaigns.Collaborate with cross-functional teams: work closely with marketing, medical, and...

What will you deal with: Manage promotional materials: ensure that all promotional contents and initiatives for pharmaceutical products complies with regulatory requirements and industry standards, overseeing the approval process before materials are used in marketing campaigns. Collaborate with cross-functional teams: work closely with marketing, medical,...

**What will you deal with**: **Manage promotional materials**: ensure that all promotional contents and initiatives for pharmaceutical products complies with regulatory requirements and industry standards, overseeing the approval process before materials are used in marketing campaigns. **Collaborate with cross-functional teams**: work closely with...

What will you deal with: Manage promotional materials: ensure that all promotional contents and initiatives for pharmaceutical products complies with regulatory requirements and industry standards, overseeing the approval process before materials are used in marketing campaigns.Collaborate with cross-functional teams: work closely with marketing, medical,...

**What will you deal with**:**Manage promotional materials**: ensure that all promotional contents and initiatives for pharmaceutical products complies with regulatory requirements and industry standards, overseeing the approval process before materials are used in marketing campaigns.**Collaborate with cross-functional teams**: work closely with marketing,...

Tasks and Responsibilities: Prepares the strategy, the technical documentation, performs the submission (through national and EU portals) and follow-up until approval of MRP, DCP, CP and National Procedures for new marketing authorizations, variations, marketing authorization transfers and renewals according to the relevant EU Regulation and national...

What will you deal with: Manage promotional materials: ensure that all promotional contents and initiatives for pharmaceutical products complies with regulatory requirements and industry standards, overseeing the approval process before materials are used in marketing campaigns. Collaborate with cross-functional teams: work closely with marketing,...

**Tasks and Responsibilities**: Revises promotional/informative/medical materials from a regulatory point of view according to Italian regulations and codes, and performs the submission to the authorities. Transmits the promotional materials through the AIFA portal. Gives support for diseases awareness materials/medical materials/press release/market...

Tasks and Responsibilities:Revises promotional/informative/medical materials from a regulatory point of view according to Italian regulations and codes, and performs the submission to the authorities.Transmits the promotional materials through the AIFA portal.Gives support for diseases awareness materials/medical materials/press release/market research, and...

Tasks and Responsibilities: Revises promotional/informative/medical materials from a regulatory point of view according to Italian regulations and codes, and performs the submission to the authorities.Transmits the promotional materials through the AIFA portal.Gives support for diseases awareness materials/medical materials/press release/market research, and...

Tasks and Responsibilities: Revises promotional/informative/medical materials from a regulatory point of view according to Italian regulations and codes, and performs the submission to the authorities. Transmits the promotional materials through the AIFA portal. Gives support for diseases awareness materials/medical materials/press release/market research,...

**Tasks and Responsibilities**:Revises promotional/informative/medical materials from a regulatory point of view according to Italian regulations and codes, and performs the submission to the authorities.Transmits the promotional materials through the AIFA portal.Gives support for diseases awareness materials/medical materials/press release/market research,...