Clinical Research Specialist

About the RoleWe are seeking a highly skilled Clinical Research Associate to join our team at IQVIA Argentina. As a Clinical Research Associate, you will be responsible for conducting site management and monitoring visits to ensure that sites are conducting clinical trials in accordance with contracted scope of work and regulatory requirements.Key...

Job Overview">At IQVIA, we are seeking a highly skilled Clinical Research Associate to join our team. As a key member of our site management team, you will be responsible for ensuring the smooth conduct of clinical trials at our partner sites.">We are looking for a professional with strong knowledge of Good Clinical Practice (GCP) and International...

Job OverviewPerform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.Essential FunctionsPerform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with...

Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with...

Job OverviewIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.Key ResponsibilitiesPerform site monitoring visits to ensure compliance with contracted scope of work and regulatory requirements.Work with sites to adapt and drive subject recruitment...

Job OverviewWe are seeking a highly skilled Clinical Research Associate to join our team at IQVIA Argentina. As a key member of our team, you will be responsible for ensuring that study sites conduct the study and report data as required by the study protocol, regulations, and sponsor requirements.

Job OverviewClinical Research Associates play a pivotal role in ensuring the success of clinical trials by conducting site monitoring visits, managing study data, and adhering to regulatory requirements. This position involves working closely with sites to adapt and drive subject recruitment plans, administer protocol training, and evaluate site...

Job SummaryWe are seeking a highly motivated Clinical Trials Coordinator to join our team at IQVIA. As a key member of our site management team, you will be responsible for ensuring the smooth execution of clinical trials. Your primary focus will be on site management, where you will work closely with research sites to ensure they are conducting studies in...

About the RoleIQVIA is seeking a Regulatory Compliance Manager - Clinical Trials to join our team in Argentina. As a Regulatory Compliance Manager, you will be responsible for ensuring that our clinical trial operations comply with regulatory requirements and guidelines.Key ResponsibilitiesDevelop and implement regulatory compliance strategies to ensure...

Job OverviewAs a Research Project Manager at IQVIA, you will be responsible for ensuring the successful execution of clinical trials. Your primary focus will be on site management, where you will work closely with research sites to ensure they are conducting studies in accordance with regulatory requirements and study protocols.Key Responsibilities:Site...

About the RoleAs a Clinical Research Associate, you will be responsible for performing site monitoring visits, tracking regulatory submissions, and managing study data. You will work closely with sites to develop and implement subject recruitment plans and ensure compliance with Good Clinical Practice (GCP) and International Conference on Harmonization (ICH)...

Job RoleWe are looking for a talented Site Management Specialist to join our team at IQVIA. In this role, you will be responsible for managing clinical trials from initiation to close-out. Your primary focus will be on site management, where you will work closely with research sites to ensure they are conducting studies in accordance with regulatory...

About the Position">This Clinical Research Associate role is a key position within our site management team. The successful candidate will be responsible for ensuring the smooth conduct of clinical trials at our partner sites.">You will be responsible for performing monitoring and site management work to ensure compliance with Good Clinical Practice (GCP)...

About This RoleThis is an exciting opportunity to work in a dynamic environment with a leading global provider of clinical research services. As a Clinical Research Associate, you will have the chance to develop your skills and expertise in study site management, regulatory compliance, and project execution.Our ideal candidate will have a strong background...

Job DescriptionWe are looking for an experienced Clinical Research Associate to join our team at IQVIA Argentina. The successful candidate will be responsible for ensuring the quality and integrity of clinical trials conducted at our partner sites.ResponsibilitiesPerform site initiation, monitoring, and close-out visits to ensure compliance with study...

About the RoleThe Clinical Research Associate will be responsible for performing site monitoring visits to ensure compliance with contracted scope of work and regulatory requirements.Main AccountabilitiesConduct site initiation visits to ensure understanding of the protocol and related procedures.Monitor study sites to ensure adherence to Good Clinical...

Job OverviewThis role is responsible for executing site identification, regulatory, start-up, and maintenance activities in accordance with regulations, SOPs, and project requirements at the regional or country level. Essential Functions:Serve as a Single Point of Contact (SPOC) to perform feasibility, site activation, and some maintenance activities in...

About the RoleWe are seeking a Site Management Coordinator to join our team at IQVIA Argentina. As a Site Management Coordinator, you will be responsible for coordinating site management activities and ensuring that clinical trials are conducted in accordance with contracted scope of work and regulatory requirements.Key ResponsibilitiesCoordinate site...

Clinical Research AssociateWorking Model:Hong Kong Client Office basedAs a Clinical Research Associate, you will be joining the world's largest & most comprehensive clinical research organization, powered by healthcare intelligence.What you will be doing:Site MonitoringSite ManagementUltimately responsible for the successful management of investigator sites...

About this roleWe are seeking an experienced professional to lead our site activation efforts in Latin America. The ideal candidate will have a strong understanding of clinical research regulations and procedures.Key responsibilities:Execute site identification, regulatory, start-up, and maintenance activities in accordance with regulations, SOPs, and...