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Cmc Jobs In Argentina - 9 Job Positions Available

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1 – 8 of 9 jobs
Syneos Health jobs

Regulatory CMC Manager Cell and Gene Therapy Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping

Syneos Health  8 days ago
IQVIA jobs

Key Responsibilities · Serve as Regulatory Team Lead on complex global studies, including oversight of technical writing and submission publishing. · Draft, review, and quality-check clinical trial regulatory core study documentation at global and country level

IQVIA  16 days ago
PAREXEL jobs

When our values align, theres no limit to what we can achieve. Join Our Growing Team of CMC Regulatory Professionals! The Senior Regulatory Associate will author global CMC variation submissions, annual reports, renewals, and post-approval MAA roll-outs, including

PAREXEL  2 days ago

Analista de desarrollo farmacéutico Importante laboratorio con presencial internacional se encuentra en búsqueda de un/a Farmacéutico/a especializado/a para integrarse al equipo de Desarrollo Farmacéutico. Si tenés experiencia en el desarrollo de productos farmacéuticos y una pasión

Pacifica Continental  2 days ago
PAREXEL jobs

When our values align, theres no limit to what we can achieve. Position Overview The Regulatory Submission Coordinator – Associate/ Sr Associate level - supports the execution and coordination of regulatory submission and labeling activities across

PAREXEL  2 days ago
Michael Page jobs

Colaborar en las estrategias regulatorias para la presentación de NDAs y ensayos clínicos Ejecutar las presentaciones regulatorias a nivel local. Participar en la revisión y formulación de la estrategia regulatoria del ciclo de vida a nivel

Michael Page  2 days ago

Para Importante Laboratorio estamos buscando un/a Farmacéutico/a especializado/a en desarrollo farmacéutico para unirse a nuestro equipo de I+D. Si tienes experiencia en la creación de productos farmacéuticos y te apasiona la innovación y la mejora de

REKLUT  1 day ago
IQVIA jobs

Key Responsibilities · Serve as Regulatory Team Lead on complex global studies, including oversight of technical writing and submission publishing. · Draft, review, and quality-check clinical trial regulatory core study documentation at global and country level

IQVIA  2 days ago

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