Job Description
IQVIA in Barcelona is seeking a Director of Regulatory Affairs to lead regulatory strategy and project management for drug development.
¿Tiene las habilidades necesarias para este puesto? Lea todos los detalles a continuación y presente su candidatura hoy mismo.
The ideal candidate will have a Master’s degree in Life Sciences and at least 8 years of regulatory experience in both US and EU markets.
Responsibilities include authoring key regulatory submissions, providing project leadership, and mentoring junior team members. xhfqzwm
This role requires strong client-facing skills and experience leading complex, cross-functional teams to drive drug development projects successfully.
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¿Tiene las habilidades necesarias para este puesto? Lea todos los detalles a continuación y presente su candidatura hoy mismo.
The ideal candidate will have a Master’s degree in Life Sciences and at least 8 years of regulatory experience in both US and EU markets.
Responsibilities include authoring key regulatory submissions, providing project leadership, and mentoring junior team members. xhfqzwm
This role requires strong client-facing skills and experience leading complex, cross-functional teams to drive drug development projects successfully.
#J-18808-Ljbffr