Study Site Management Expert

About the Role">This is an exciting opportunity to join our site management team as a Clinical Research Associate. In this role, you will be responsible for ensuring the smooth conduct of clinical trials at our partner sites.">You will work closely with sites to ensure they are conducting the study(ies) and reporting study data as required by the study...

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 RoleThe Clinical Research Associate role is responsible for ensuring the quality and integrity of clinical trials conducted at our partner sites. This includes monitoring and managing site activities, ensuring compliance with study protocols and regulations, and collaborating with internal teams to drive study execution.ResponsibilitiesPerform site...

Key ResponsibilitiesConduct site monitoring visits to ensure sites are conducting studies and reporting data as required.Work with sites to adapt and drive subject recruitment plans to meet project needs.Administer protocol training and establish regular lines of communication with sites.Evaluate site practices and escalate quality issues as necessary.Manage...

Job SummaryWe are seeking a highly skilled Clinical Research Associate to join our team at IQVIA Argentina.Key DutiesPerform site monitoring visits to ensure compliance with contractual obligations and regulatory requirements.Develop and maintain relationships with study sites and investigators.Provide training and support to sites on protocol and study...

Clinical Research Associate Position SummaryWe are seeking a highly motivated and experienced Clinical Research Associate to join our team at IQVIA Argentina. As a key member of our clinical operations team, you will be responsible for ensuring the smooth conduct of clinical trials at research sites across the country.Main Responsibilities:Performing site...

Site Monitoring and Management RoleWe are seeking an experienced Clinical Research Associate to join our team at IQVIA Argentina. As a key member of our clinical operations team, you will be responsible for ensuring the smooth conduct of clinical trials at research sites across the country.Your Key Responsibilities Will Include:Conducting site initiation,...

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 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 OverviewUnder moderate supervision, executes the feasibility, site identification, regulatory, start-up, and maintenance activities in accordance with regulations, SOPs, and project requirements at the regional or country level. Prepares and manages site documentation; reviews and negotiates site documents and contracts with sites and sponsors;...

Job Overview Under moderate supervision, executes the feasibility, site identification, regulatory, start-up, and maintenance activities in accordance with regulations, SOPs, and project requirements at the regional or country level. Prepares and manages site documentation; reviews and negotiates site documents and contracts with sites and sponsors;...

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...

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 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 OverviewAs a Clinical Research Associate at IQVIA Argentina, you will be responsible for ensuring that sites conducting clinical studies are following Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.Key ResponsibilitiesPerform site monitoring visits to assess compliance with study protocols and regulatory...

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...

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)...

Job OverviewIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments.Key Responsibilities:Perform site monitoring visits to ensure...

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...