Pan-American Clinical Regulatory Specialist

Knight aspires to be the leading Pan-American (ex-US) partner of choice, with a growing portfolio of innovative and high-quality branded products. The Global Clinical Regulatory Associate will enable this corporate ambition, by contributing directly or indirectly to its strategic priorities: in-licensing and developing new products across Pan-American...

Site Specialist II ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers. We are...

Senior Regulatory and Start Up Specialist (Argentina) Remote, Argentina We’re expanding our capabilities across Mexico, Brazil, Argentina, Colombia, Chile, and Peru , and we’re hiring our first Senior Regulatory and Start Up Specialist (Senior RSS) in Argentina! As the Senior RSS on our team, you are a seasoned, experienced professional in regulatory and...

Indero is a contract research organization (CRO) focused on dermatology and Rheumatology, based in Montreal with international reach, now seeking a Legal Specialist to support the Legal Department in Argentina. The role covers contracts, governance, and regulatory compliance for clinical research activities.You will prepare, review, and administer CTAs,...

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....

The Legal Specialist supports the Legal Department in providing efficient, accurate, and timely legal and administrative assistance related to the Company’s clinical research operations. The role contributes to contract management, corporate governance, regulatory compliance support, and legal documentation, in alignment with applicable laws,...

Precision Medicine Group is seeking a Senior Regulatory and Start Up Specialist for Argentina to lead regulatory submissions, start-up activities, and country-specific documentation across clinical studies. This remote role focuses on timely activation and compliance with local and international guidelines.You will collaborate with CA/EC, prepare submission...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Country Approval Specialist – Make an Impact at the Forefront of InnovationWe have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years. ...

IQVIA is seeking a Site Activation specialist to support feasibility, regulatory start-up, and maintenance activities at regional or country levels for investigative sites.You will prepare site documents, coordinate with sites and sponsors, and track timelines to ensure contracts and regulatory requirements are met.Based in Argentina or Brazil, you will work...