Regulatory Affairs Specialist — Mid Level

David Kennedy Recruitment; Partido de Quilmes; Remote; ARS 63.808.000 - 100.270.000; Vollzeit

Zusammenfassung

IQVIA is hiring a Regulatory Affairs Officer (Mid Level) to prepare and review regulatory submissions for clinical trials and marketing authorization activities. You will support assigned projects, work with cross-functional teams, and help ensure compliance with regulatory standards across multiple regions.

Qualified candidates have a Lifesciences degree, 2-3 years in regulatory affairs, and fluent English.

Qualifikationen

• Bachelor's degree in lifescience or related discipline is required.
• 2-3 years of regulatory affairs (postmarketing) experience.
• Fluent English: spoken, reading and writing.

Aufgaben

• Acts as Regulatory Team Member on small projects under senior guidance.
• Identifies needs, tracks timelines and manages day-to-day workload with senior staff.
• Prepares and/or reviews regulatory documentation in area of expertise as appropriate.
• Communicates effectively with internal/external stakeholders in straightforward matters.

Kenntnisse

Fluent English

Regulatory knowledge

Microsoft Office

Ausbildung

Bachelor's Degree in Life sciences or related discipline

Tools

Microsoft Office

Jobbeschreibung

IQVIA is hiring a Regulatory Affairs Officer (Mid Level) to prepare and review regulatory submissions for clinical trials and marketing authorization activities. You will support assigned projects, work with cross-functional teams, and help ensure compliance with regulatory standards across multiple regions.

Qualified candidates have a Lifesciences degree, 2-3 years in regulatory affairs, and fluent English.