Senior Site Start-Up Leader

**Parexel FSP** is looking for** Global Site Start-up II**in **Argentina**! **Job Summary** The Global Site Start-up II is accountable for the global execution of site activation for assigned clinical trials, performing responsibilities with moderate oversight. The Global Site Start-up II is accountable for ensuring site start-up is efficient, timely and...

Role Description Study-Start-Up/QC Specialist: Purpose: Study Start Up/QC Specialist is responsible for country study start up (SSU) activities and performing quality review of essential documents. The SSU/QC Specialist is responsible for overseeing and leading SSU activities in collaboration with country team members (CLM and CRA) with the objective to...

Senior Specialist Country Study Start Up AbbVie Company Description The Sr. Specialist, Country Study Start Up proactively drives and executes all start up and maintenance related activities and deliverables for assigned studies and sites in their assigned country or countries. The Sr. Specialist, Country SSU is responsible and accountable for on-time,...

A global biopharmaceutical company is seeking a Senior Specialist Country Study Start Up to drive start-up and maintenance activities for clinical studies. The ideal candidate will have at least 3 years of experience in clinical research and strong expertise in site activation plans. Responsibilities include coordinating with IRB/EC sites, maintaining...

A leading biopharmaceutical solutions organization is seeking a Site Activation Specialist based in Argentina. This role involves managing the site identification process across multiple countries, ensuring compliance with regulations, and maintaining performance metrics. The ideal candidate will have a relevant bachelor's degree and at least 3 years of...

We are looking for a Regulatory & Start Up Specialist to join our FSP team in a Home Based role! What You’ll Do Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary...

A global clinical research provider is seeking a Senior Study Start up Specialist to perform site activation activities in Buenos Aires. The ideal candidate will have at least a Bachelor's degree in life sciences and 3 years of clinical research experience, including leadership. Key responsibilities include being the Main Point of Contact for sites, ensuring...

Start Up Manager ICON plc is a world‑leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. We are currently seeking a Manager, Study Start‑Up to join our diverse and...

Start Up ManagerICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical developmentWe are currently seeking a Manager, Study Start-Up to join our diverse and dynamic...

Job Summary: Our LATAM clinical trial activities are growing rapidly, and we are currently seeking a full-time, office-based **Regulatory Submissions Manager** to join our Study Start Up team in Buenos Aires! This position plays a key role in the study start up process at Medpace. If you want an exciting career where you use your previous expertise and can...