Regulatory Affairs Lead – Clinical Development

10 ore fa


Turbigo, Italia Option One Life Science Consulting Sagl A tempo pieno

A leading life science consulting firm is seeking a Regulatory Affairs Manager to support global clinical development programs. The ideal candidate will have 7-10 years of experience in the pharmaceutical industry, with a strong background in managing clinical trial applications, including CTA/IND submissions and compliance with regulatory requirements across EU, US, and RoW. Key skills include regulatory strategy development, regulatory intelligence, and effective communication with regulatory agencies, contributing to the advancement of innovative therapies.#J-18808-Ljbffr



  • turbigo, Italia Option One Life Science Consulting Sagl A tempo pieno

    A leading life science consulting firm is seeking a Regulatory Affairs Manager to support global clinical development programs. The ideal candidate will have 7-10 years of experience in the pharmaceutical industry, with a strong background in managing clinical trial applications, including CTA/IND submissions and compliance with regulatory requirements...


  • Turbigo, Italia Option One Life Science Consulting Sagl A tempo pieno

    Regulatory Affairs Manager | Clinical Development (CTA/IND) | EU/US/RoW ABOUT / INFO Regulatory Affairs professional with 7 - 10 years of experience in the pharmaceutical industry, supporting global clinical development programs across EU, US and RoW. Strong track record in managing clinical trial applications and maintenance activities (CTA/IND),...


  • Turbigo, Italia Option One Life Science Consulting Sagl A tempo pieno

    Regulatory Affairs Manager | Clinical Development (CTA/IND) | EU/US/RoWABOUT / INFORegulatory Affairs professional with 7 - 10 years of experience in the pharmaceutical industry, supporting global clinical development programs across EU, US and RoW. Strong track record in managing clinical trial applications and maintenance activities (CTA/IND), coordinating...


  • turbigo, Italia Option One Life Science Consulting Sagl A tempo pieno

    Regulatory Affairs Manager | Clinical Development (CTA/IND) | EU/US/RoWABOUT / INFORegulatory Affairs professional with 7 - 10 years of experience in the pharmaceutical industry, supporting global clinical development programs across EU, US and RoW. Strong track record in managing clinical trial applications and maintenance activities (CTA/IND), coordinating...


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  • Clinical Project Lead

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  • turbigo, Italia Sobi A tempo pieno

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