Regulatory Submissions Specialist — Trials & MA

IQVIA; Ciudad de México; Presencial; MXN 420.000 - 600.000; Jornada completa

Descripción de la vacante

IQVIA in Mexico City is seeking a Regulatory Affairs professional to prepare and review regulatory submission documents supporting clinical trials and marketing authorizations for internal or external clients. You will contribute to regulatory activities under general supervision and collaborate with global teams to ensure timely, compliant submissions.

The role emphasizes knowledge of Chemistry, Manufacturing and Controls, labeling, publishing, and lifecycle maintenance, with opportunities to

Formación

• Bachelor's degree in life sciences or related field.
• At least 2 years of regulatory affairs experience.
• Fluent English in speaking, reading and writing.

Responsabilidades

• Acts as Regulatory Team Member on small, straightforward projects.
• Identifies project needs, tracks timelines, and supports client requests.
• Maintains knowledge of regulatory processes and related submissions.
• Prepares and reviews regulatory documentation within expertise.
• Participates in project teams and client meetings as needed.
• Supports training delivery and process improvements.

Conocimientos

Regulatory affairs

English proficiency

Project coordination

Microsoft Office

Interpersonal communication

Educación

Bachelor's Degree in Lifescience or related discipline

Descripción del empleo

IQVIA in Mexico City is seeking a Regulatory Affairs professional to prepare and review regulatory submission documents supporting clinical trials and marketing authorizations for internal or external clients. You will contribute to regulatory activities under general supervision and collaborate with global teams to ensure timely, compliant submissions.

The role emphasizes knowledge of Chemistry, Manufacturing and Controls, labeling, publishing, and lifecycle maintenance, with opportunities to