Regulatory Submissions Specialist — Clinical Research

A global clinical research organization is seeking a Clinical Project Manager to oversee clinical trials in Neuquén, Argentina. The ideal candidate will have a Bachelor's degree in allied health fields and at least 6 years of clinical research experience. Responsibilities include project management from planning to execution, ensuring compliance with...

A leading global healthcare technology company is seeking a Regulatory Affairs Specialist in Argentina to manage regulatory submissions, ensure compliance, and liaise with regulatory agencies. The role requires a Bachelor's degree and a minimum of 2 years of experience in the medical devices or pharmaceutical industry. The candidate must be fluent in English...

Clinical Research Associate - All Levels Join Medpace in Buenos Aires! The Clinical Research Associate at Medpace is offering the unique opportunity to have an exciting career in the research of drug and medical device development. For those with medical and/or health/life science interest and background who want to explore the research field, travel...

A leading global provider of clinical research services is seeking a Senior Regulatory and Start Up Specialist in Chubut, Argentina. The role entails performing site activation activities in compliance with local and international regulations, overseeing project timelines, and ensuring quality control of documents. Candidates must hold a Bachelor's degree in...

Regulatory Affairs Specialist /Argentina At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world. A Day in the Life We’re a mission-driven leader in medical technology...

Clinical Project Manager – Level Dependent on Experience CTI Clinical Trial and Consulting Services is a global, privately held, full‑service clinical contract research organization (CRO) focused on the advancement of treatments for chronically and critically ill patient populations. We assist clinical research throughout the life‑cycle of development,...

Get AI-powered advice on this job and more exclusive features. Join Medpace in our Buenos Aires office! As a Regulatory Submissions Coordinator you will have the opportunity to work within Regulatory Submissions, supporting our many projects and gaining some vital experience. You will be a productive member of the team and will be mentored and supported as...

Job Overview Clinical Research Associate role at MSD LATAM – a global health care leader. The position is accountable for performance and compliance for assigned protocols and sites in Argentina. Under the oversight of the CRA manager the person ensures compliance of study conduct with ICH/GCP and country regulations, company policies and procedures,...

Job DescriptionThe Clinical Research Director serves as the Clinical Operations lead for a country or cluster of countries and is responsible for the execution of all clinical trials within the scope of the Global Clinical Trial Operations country organization. This leader ensures trials are conducted to high quality standards and are inspection ready, in...

A leading global clinical research company is seeking a Senior Clinical Research Associate (CRA) in Chubut, Argentina. The role involves planning, executing, and managing clinical trials to ensure data integrity and regulatory compliance. Candidates must have a Bachelor's degree in a relevant field and at least 4 years of on-site monitoring experience....