LATAM Study Start-Up Regulatory Manager

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...

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 clinical trial management process at Medpace. If you want an exciting career where you use your previous...

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...

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...

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...

Unleash Your Potential It takes curiosity and intellectual courage to accomplish great things. It takes brave minds to bring powerful ideas to reality and transform healthcare. We are a diverse, global team that shares a passion for collaboration and solving complex problems. Together, we help customers drive healthcare forward. Join IQVIA and see where...

Study Start Up Associate II 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. Responsibilities: Proficient knowledge of ICON SOPs/WPs, ICH/GCP and...

Job OverviewDirect and manage the delivery of all required site activation, maintenance and regulatory activities for selected studies or multi-protocol programs, including pre-award activities, oversight of the scope of work, budget and resources. Essential Functions• Oversee the execution of Site Activation (including pre-award/bid defense activities)...

100,000. That’s how many patients participate in our clinical trials at any given time. Global Clinical Operations (GCO) touches patients’ lives every day acting as a link between science and medicine. Envision the impact you could have! #GCO Site relationship management role to ensure sustainable trial start-up at Site. The Study Start-Up CRA is...

At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives. Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery,...