Research Project Manager

CHINA MOBILE HONG KONG COMPANY LIMITED ("CMHK") is the wholly-owned subsidiary of China Mobile Limited (HKEx: 941), which ranks 55th on the Fortune Global 500.Our company strives to offer superior service experience and to become a first-class service provider in the development of digitalized and intelligent Hong Kong. We are preserving an environment with...

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...

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...

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 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 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 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...

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 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 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 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...

Arcon System Limited is a leading player in the technology industry, and we are currently seeking an experienced Administrative Lead for Projects to join our team. In this critical role, you will provide strategic support to our project management team, driving project success through exceptional leadership and coordination.Your key responsibilities will...

We are committed to being an equal opportunity employer and offer an exceptional benefits package to our employees.About UsChina Mobile Hong Kong is a wholly-owned subsidiary of China Mobile Limited, ranking 55th on the Fortune Global 500. We strive to offer superior service experience and become a first-class service provider in the development of...

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 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 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...

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...

We are looking for an experienced Project Support Specialist to support our project management team at Arcon System Limited. As a key member of our team, you will play a vital role in ensuring the successful completion of our projects.Your primary responsibilities will include:Monitoring project progress and providing regular updates to the project...