Regulatory Affairs Specialist — Mid Level

David Kennedy Recruitment; Partido de Quilmes; On-site; ARS 63,808,000 - 103,309,000; Full time

Job summary

IQVIA is seeking a Regulatory Affairs Officer at a mid level to support regulatory submissions for clinical trials and marketing authorization. You will work with internal and external clients under supervision, ensuring regulatory compliance across multiple regions and maintaining project timelines.

The role requires a Lifescience degree, 2-3 years of postmarketing experience, and strong English communication. Collaboration with global teams and training activities may be involved.

Qualifications

• Bachelor’s degree in Lifescience or related discipline.
• 2-3 years of regulatory affairs postmarketing experience.
• 1 year tracking information on regulatory processes.
• Fluent English: spoken, read and written.
• Experience with multiple countries (USA, Canada) is a plus.

Responsibilities

• Prepare and/or review regulatory submissions documents for trials and MA activities.
• Act as Regulatory Team member on small projects under supervision.
• Identify project needs, track timelines and manage workload with seniors.
• Participate in client meetings and deliver trainings as appropriate.

Skills

Regulatory experience

English fluency

Interpersonal skills

Regulatory monitoring

Documentation & publishing

Education

Bachelor's in Life Sciences

Tools

Microsoft Office

Job description

IQVIA is seeking a Regulatory Affairs Officer at a mid level to support regulatory submissions for clinical trials and marketing authorization. You will work with internal and external clients under supervision, ensuring regulatory compliance across multiple regions and maintaining project timelines.

The role requires a Lifescience degree, 2-3 years of postmarketing experience, and strong English communication. Collaboration with global teams and training activities may be involved.