Regulatory Submissions

A global clinical research organization is seeking a Country Approval Specialist based in Buenos Aires, Argentina. This role is essential for coordinating regulatory submissions and ensuring site activation. The successful candidate will need a Bachelor's degree and at least 2 years of relevant experience. Key skills include attention to detail, effective...

Regulatory Submissions Specialist (with Portuguese) IQVIA This role will require special working days as National Holidays and weekends. Job Overview As a Regulatory Reporting Specialist, you will be involved in submitting safety reports to regulatory authorities. Review, assess, and process safety data and information received from various sources....

This role will require special working days as National Holidays and weekends. _ Job Overview - As a Regulatory Reporting Specialist, you will be involved in submitting safety reports to regulatory authorities. _ Review, assess, and process safety data and information received from various sources. Distribute reports/data to internal and external third...

A global medical technology leader is seeking a Regulatory Affairs Specialist in Buenos Aires. This position requires a bachelor's degree in relevant fields and fluency in English, with over two years of regulatory affairs experience. The role involves direct coordination for regulatory submissions, compliance recommendations, and monitoring of regulatory...

**Join Amgen’s Mission of Serving Patients** At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do. Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on...

A global consulting firm is seeking a Regulatory & Start Up Specialist for a home-based role. This position requires a minimum of 2 years of clinical research experience, particularly in submitting procedures to the Ministry of Health in Argentina. The ideal candidate will possess a Health Sciences degree, a strong command of English, and experience with MoH...

A leading medical technology company is seeking a Regulatory Affairs Specialist to oversee coordination for regulatory submissions and ensure compliance in medical devices. Located in Argentina, the position offers a hybrid work model. The ideal candidate requires a Bachelor's degree in a relevant field and must have 2+ years of experience in regulatory...

A global healthcare company is searching for a Regulatory Affairs Sr Specialist to consult on documentation for submissions across LATAM markets. The role requires 3-4 years of experience in the regulatory environment and knowledge of LATAM regulations. Applicants should hold a Bachelor’s degree in life sciences. The position involves preparing...

A leading biopharmaceutical solutions organization is seeking a Regulatory Consultant CMC for Small Molecule in Buenos Aires. The role involves preparing regulatory submissions, managing project activities, and providing expertise to multidisciplinary teams. Ideal candidates should have experience with CMC in Biologics and Veeva Vault RIM. This position is...

A career at our company is an ongoing journey of discovery: our 60,300 people are shaping how the world lives, works and plays through next generation advancements in Healthcare, Life Science and Electronics. For more than 350 years and across the world we have passionately pursued our curiosity to find novel and vibrant ways of enhancing the lives of...