Remote Global Clinical Study Specialist

Overview Study Delivery Specialist - RemoteICON 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 looking for candidates who have experience in...

A global biopharmaceutical company is seeking a Clinical Study Administrator in Lombardy to coordinate clinical trial activities and ensure quality and compliance with regulations. This role requires a Bachelor's in life science and proficiency in MS Office. The ideal candidate should have strong organizational, communication, and collaboration skills. Join...

Clinical Study Administrator (CSA), Country Operations Management Apply to the Clinical Study Administrator (CSA), Country Operations Management role at Alexion Pharmaceuticals, Inc.Are you ready to make a difference in the world of clinical trials? As a Clinical Study Administrator (CSA) within Country Operations Management (COM), you'll play a pivotal role...

Are you ready to make a difference in the world of clinical trials?As a Clinical Study Administrator (CSA) within Country Operations Management (COM), you'll play a pivotal role in coordinating study activities from start-up to execution and close-out. Your mission is to ensure quality and consistency in trial deliverables, meeting time, cost, and quality...

Are you ready to make a difference in the world of clinical trials?As a Clinical Study Administrator (CSA) within Country Operations Management (COM), you'll play a pivotal role in coordinating study activities from start-up to execution and close-out. Your mission is to ensure quality and consistency in trial deliverables, meeting time, cost, and quality...

Clinical Monitoring Analyst (Cluepoints) - RemoteJoin to apply for the Clinical Monitoring Analyst (Cluepoints) - Remote role at IQVIA .This unique role within IQVIA is a Lead programmer on Cluepoints called Centralized Monitoring Analyst (CMA) and requires strong communication and organization skills. Experience with SAS programming is required.This role is...

OverviewAre you ready to make a difference in the world of clinical trials? As aSenior Clinical Study Administrator (CSA)within Country Operations Management (COM), you will coordinate study activities from start-up to execution and close-out. Your mission is to ensure quality and consistency in trial deliverables, meeting time, cost, and quality objectives...

Job Description SummaryNovartis seeks a dynamic and experienced SSO Study Start-Up Manager (SSUM) to join our dedicated team. This pivotal position reports directly to the Study Start-Up (SSU) Team Lead and leads the local Study Start-Up teams for designated trials holding significant responsibilities within our organization ranging from trial and budget...

OverviewAre you ready to make a difference in the world of clinical trials? As aCountry Study Manager (CSM) , you\'ll be at the forefront of delivering studies in compliance with Good Clinical Practice (GCP) and regulatory requirements. Collaborate closely with the Study Start-Up (SSU) manager, Clinical Study Administrator (CSA), and other CRAs in Country...

Clinical Monitoring Analyst (Cluepoints) - Remote Join to apply for theClinical Monitoring Analyst (Cluepoints) - Remoterole atIQVIA .This unique role within IQVIA is a Lead programmer on Cluepoints called Centralized Monitoring Analyst (CMA) and requires strong communication and organization skills. Experience with SAS programming is required.This role is...