Regulatory Affairs Specialist — Mid Level

IQVIA is seeking a Regulatory Affairs Officer at a mid-level to support regulatory submissions across markets. Based in Argentina with exposure to Peru and Colombia, you will prepare and review regulatory documents, track timelines, and support labeling/publishing activities under supervision.The ideal candidate has 2–3 years in regulatory affairs, fluent...

Company DescriptionMedicine moves forward here. So will you. At PrimeVigilance, patient safety is not one part of the job. It is why we exist. We are a global pharmacovigilance specialist. Our teams help clients navigate complex regulations while keeping patient safety at the center of every decision, from early development through to post-marketing...

Regulatory Affairs Officer (Mid Level Role)Lima, PeruBuenos Aires, ArgentinaBogota, ColombiaFull timeR**Job Overview**Under general supervision, Prepares and/or reviews regulatory submissions documents to support clinical trial and marketing authorization activities for either internal and/or external clients. Provides regulatory support for assigned...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Site Activation & Country Approval SpecialistMake an Impact at the Forefront of InnovationAt Thermo Fisher Scientific, our Clinical Research team supports leading pharmaceutical, biotechnology, and emerging biopharma companies in advancing innovative therapies worldwide....

CRA SSU with at least 2 years of regulatory experience - Sponsor dedicated - Argentina Client BasedSyneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.  Our Clinical...

Site Activation Specialist (US Experience) Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Every day we perform better because of how we work together, as one...

Lima, Peru Buenos Aires, Argentina Bogota, Colombia Full time R1568008 Job Overview Under general supervision, Prepares and/or reviews regulatory submissions documents to support clinical trial and marketing authorization activities for either internal and/or external clients. Provides regulatory support for assigned projects. Essential Functions Acts as a...

IQVIA is seeking a Regulatory Affairs Officer at a mid-level to support regulatory submissions across markets. Based in Argentina with exposure to Peru and Colombia, you will prepare and review regulatory documents, track timelines, and support labeling/publishing activities under supervision.The ideal candidate has 2–3 years in regulatory affairs, fluent...

Company Description Medicine moves forward here. So will you. At PrimeVigilance, patient safety is not one part of the job. It is why we exist. We are a global pharmacovigilance specialist. Our teams help clients navigate complex regulations while keeping patient safety at the center of every decision, from early development through to post-marketing...