Junior 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...

Hong Kong Metropolitan University is committed to fostering innovation and creativity in our students and staff.We strive to provide high-quality education and training that meets industry needs and prepares our graduates for rewarding careers. Our research activities focus on key areas such as digital humanities and literature, international business,...

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...

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...

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 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 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 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 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 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...

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...

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 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;...