Site Management Specialist

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;...

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...

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...

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 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...

Key Responsibilities:Site Monitoring: Perform site monitoring visits to ensure compliance with contracted scope of work and regulatory requirements.Protocol Training: Administer protocol and related study training to assigned sites and establish regular communication to manage ongoing project expectations.Quality Assurance: Evaluate the quality and integrity...

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...

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...

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 DescriptionThis position requires advanced knowledge within a specific discipline, typically gained through extensive work experience and/or education.Responsibilities include:Reviewing documents for completeness, consistency, and accuracy.Preparing site documents, including questionnaires, CDAs, regulatory, ethics, ICF, and IP release documents.Tracking...

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 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 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 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 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...

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...

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 seeking a talented individual who is passionate about joining our growth journey. This is an excellent opportunity to become a key member of our dynamic team and play an integral role in our expansion.Responsibilities:Manage HK Data Center design progress and quality.Oversee site operations and ensure work is completed on-time and...

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...

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...