Regulatory & Site Activation Lead - Clinical Trials

A leading clinical research organization is seeking a Senior Clinical Research Associate in Argentina to enhance the integrity and management of clinical trials. The ideal candidate will have at least 4 years of monitoring experience and a Bachelor's degree in a relevant field, along with advanced proficiency in English. Responsibilities include site...

Make an impact on patient health! IQVIA’s Global Site Activation Team of 2000 employees drives best in class site and customer experience, with industry leading outcomes. Home-Based - Argentina Job Overview As a Senior Site Activation Coordinator, under general supervision, you will perform tasks at a country level associated with site activation...

A leading clinical research company is seeking a Senior Site Activation Coordinator based in Argentina. This role involves performing site activation tasks according to regulations, working with various internal teams, and managing documentation. The ideal candidate will have a Bachelor’s Degree in Life Science and a minimum of 2 years of work experience...

A leading biopharmaceutical solutions organization is looking for a Site Contracts Specialist. This role involves negotiating contracts and budgets for clinical trials, administering contract management processes, and collaborating with internal and external stakeholders. Candidates should possess moderate contract management experience, strong communication...

Join to apply for the Senior Site Activation Coordinator role at IQVIA. Make an impact on patient health! Hybrid – Argentina Job Overview As a Senior Site Activation Coordinator, under general supervision, you will perform tasks at a country level associated with site activation activities. These activities will be in accordance with applicable local...

A leading global provider of clinical research services is seeking a Senior Site Activation Coordinator in Argentina. In this hybrid role, you will oversee site activation activities, support the preparation and approval of essential documents, and maintain project-specific systems. Ideal candidates will hold a Bachelor’s Degree in Life Sciences and have...

Site Readiness and Regulatory Specialist I Job Overview Primary contact with investigative sites during study maintenance and, when assigned, site startup activities, responsible for collecting required investigator and regulatory essential documents to ensure EC/IRB/Third body/Regulatory Authority submissions are made within the agreed timelines with...

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....

Join to apply for the Senior Site Activation Manager hybrid Argentina role at Syneos Health . 2 days ago – Be among the first 25 applicants. 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...

A leading global provider of clinical research services is seeking a Contract Negotiator. The role involves conducting contract negotiations with research sites and performing site activation activities while ensuring adherence to regulations. Ideal candidates will have over 2 years of clinical research experience and a degree in Health Sciences. Strong...