Regulatory Affairs Specialist: Clinical Trials

Hace 6 horas

estado de méxico IQVIA Inc Jornada completa

IQVIA is seeking a Regulatory Affairs professional to prepare and review regulatory submissions for clinical trials and marketing authorization activities. The role supports internal and external clients under general supervision, participating in project teams and client meetings as needed.

The candidate should have 2–3 years of regulatory affairs experience, a life sciences degree (BSc preferred), and fluent English.