Clinical Research Associate

Research OpportunityHong Kong Metropolitan University invites applications for the position of Part-time Research Associate/Assistant I/II/Technical Assistant (Project No: R2081), focusing on the research project 'Dealing with Deceptive and Misleading Advertising Practices in Livestream Selling with Influencers in China.'The successful candidate will work...

Job DescriptionTemporary Research Assistant I/II (Several Posts) - Job Summary:Assist research teams on various projects, including participant recruitment, data collection, and literature reviews.Conduct data processing and analysis using SPSS.Provide administrative support, including preparation of progress updates and meeting minutes.This is an exciting...

Job SummaryThis 18-month accelerated learning program offers a stimulating career opportunity with the market leader in industrial and electronic engineering.Comprehensive on-the-job learning and coaching with formal training.Hands-on experience in research and development of innovative solutions within car parking and other modern IoT technology.

Join Our TeamWe are currently seeking a highly skilled and dedicated individual to fill the role of Part-time Research Associate/Assistant I/II/Technical Assistant (Project No: R2081) at Hong Kong Metropolitan University.The successful candidate will have a strong background in law or a related discipline and prior experience in legal research or a related...

Key ResponsibilitiesThe Data Analysis and Reporting Associate will be responsible for performing quantitative data analysis, writing reports for statistical results, and providing assistance in project coordination. The successful candidate will have a bachelor's degree (research assistant II) or master's degree (research assistant I) in statistics or a...

Job OverviewHong Kong Metropolitan University is seeking a highly motivated and detail-oriented individual to join our research team as a Part-time Research Associate/Assistant I/II/Technical Assistant (Project No: R2081).The appointee will be responsible for conducting literature reviews, collecting data from various sources, and assisting with other...

Job Description - Part-time Research Associate/Assistant I/II/Technical Assistant (Project No: R2081) (B&A) (25000GL)Founded in 1989, Hong Kong Metropolitan University (HKMU) is a modern, vibrant and dynamic university. We tailor our professional programmes to adapt to market trends and meet industry needs, thus providing our students with quality...

Job Description - Part-time Research Associate/Assistant I/II/Technical Assistant (Project No: R2081) (B&A) (25000GL) Founded in 1989, Hong Kong Metropolitan University (HKMU) is a modern, vibrant and dynamic university. We tailor our professional programmes to adapt to market trends and meet industry needs, thus providing our students with quality...

Requirements and QualificationsA recognized Bachelor's degree or above, preferably in healthcare, psychology, statistics, or related disciplinesExperience in mindfulness practice will be an advantageProficient in MS Office Words, Excel, and PowerPoint; proficient in SPSS will be an advantageA good command of written and spoken English and ChineseA strong...

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 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 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 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...

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 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 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 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 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...

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 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 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 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 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...

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...

Role SummaryWe 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 quality and integrity of clinical trials conducted at our partner sites.Key ActivitiesConduct site initiation, monitoring, and close-out visits to assess...