Clinical Study Specialist

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...

Job Description">We are seeking a highly skilled Clinical Trials Specialist to join our team in Argentina. The successful candidate will be responsible for managing the quality and integrity of study site practices related to the proper conduct of clinical trials.">Main Responsibilities">Evaluate the quality and integrity of study site practices related to...

Role Overview">The Clinical Trials Specialist will be responsible for managing the quality and integrity of study site practices related to the proper conduct of clinical trials. This includes performing site monitoring visits, evaluating the quality and integrity of study site practices, and ensuring compliance with applicable regulations and...

About the Role:The Clinical Research Associate will be responsible for ensuring the smooth execution of clinical trials at designated sites. Key responsibilities include conducting site monitoring visits, collaborating with sites on subject recruitment plans, providing protocol training, evaluating site practices, managing study progress, and maintaining...

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...

About the Role">This role is responsible for ensuring the quality and integrity of study site practices related to the proper conduct of clinical trials. The successful candidate will work closely with sites to adapt, drive, and track subject recruitment plans in line with project needs.">Main Responsibilities">Perform site monitoring visits (selection,...

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...

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 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 OverviewIQVIA Argentina seeks a Site Activation Specialist to execute feasibility, site identification, regulatory, start-up, and maintenance activities in accordance with regulations, SOPs, and project requirements at the regional or country level. The ideal candidate will prepare and manage site documentation; review and negotiate site documents and...

Job Summary">We are seeking a highly skilled Clinical Trials Specialist to join our team in Argentina. The successful candidate will be responsible for managing the quality and integrity of study site practices related to the proper conduct of clinical trials.">Main Accountabilities">Collaborate with study team members to ensure the successful execution of...

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 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 Overview:Clinical Research Associates play a vital role in ensuring the successful execution of clinical trials. This position is responsible for conducting site management work to guarantee that sites are conducting studies and reporting data as required by the study protocol, applicable regulations, and sponsor requirements.Key Responsibilities:Perform...

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,...

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...

Job Description:This position is responsible for site management work to ensure that sites are conducting studies and reporting data as required by the study protocol, applicable regulations, and sponsor requirements. Key responsibilities include conducting site monitoring visits, collaborating with sites on subject recruitment plans, providing protocol...

SR Clinical Operations Specialist (Regulatory Submission, Sponsor base, Hong Kong)Updated: February 19, 2025 Location: Hong Kong (Greater China)-Asia Pacific - HKG-Client-Based Job ID:25001881 Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical...

About IQVIA ArgentinaWe are a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. Our Site Activation Specialist will play a crucial role in supporting our clients' research efforts by executing site activation activities in accordance with regulations, SOPs, and project...

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;...