
Regulatory Publishing Lead (eCTD/Submissions) Job at Pharmatech Associates in Lo
Pharmatech Associates, Los Angeles, CA, United States
A leading regulatory consulting firm is seeking an experienced professional to manage regulatory submissions including INDs and NDAs. The ideal candidate must hold a Bachelor's degree and have over 5 years of relevant experience, strong knowledge of FDA regulations, and expertise in electronic submission tools. The role requires excellent project management and communication skills to collaborate with internal teams and clients effectively, ensuring quality and accuracy in submissions.
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In Summary: The ideal candidate must hold a Bachelor's degree and have over 5 years of relevant experience, strong knowledge of FDA regulations, and expertise in electronic submission tools . The role requires excellent project management and communication skills to collaborate with internal teams and clients effectively .
En Español: Una empresa líder de consultoría regulatoria está buscando un profesional experimentado para gestionar los envíos regulatorios, incluidos IND y NDA. El candidato ideal debe tener una licenciatura y tener más de 5 años de experiencia relevante, un sólido conocimiento de las regulaciones de la FDA y experiencia en herramientas electrónicas de presentación.