Site Monitoring and Management Professional
4 days ago
Job Summary
IQVIA is seeking a skilled Clinical Research Associate to join our team in IQVIA Argentina. As a key member of our site management team, you will be responsible for ensuring that clinical trials are conducted efficiently and effectively at study sites.
Key Functions
- Perform site monitoring visits to ensure compliance with GCP and ICH guidelines.
- Work with site personnel to develop and track subject recruitment plans.
- Provide protocol and study training to assigned sites and establish regular communication to manage ongoing project expectations and issues.
- Evaluate the quality and integrity of study site practices related to the conduct of clinical trials and adherence to applicable regulations.
- Manage study progress by tracking regulatory submissions and approvals, case report form completion and submission, and data query generation and resolution.
- Maintain accurate documentation regarding site management, monitoring visit findings, and action plans.
- Collaborate with study team members to support project execution as needed.
Qualifications
- Bachelor's degree in a scientific discipline or healthcare field preferred.
- At least 1 year of on-site monitoring experience required.
- Good knowledge of clinical research regulatory requirements, including GCP and ICH guidelines.
- Excellent therapeutic and protocol knowledge as provided in company training.
- Proficiency in Microsoft Office and other relevant software applications.
- Strong written and verbal communication skills, including a good command of the English language.
- Organizational and problem-solving skills, with ability to establish effective working relationships with colleagues, managers, and clients.
What We Offer
We offer a competitive compensation package, comprehensive benefits, and opportunities for professional growth and development.
Join us and become part of a talented team of professionals dedicated to improving patient outcomes and population health worldwide.
-
Site Management Specialist
2 days ago
kwai tsing district, Hong Kong SAR China IQVIA Argentina Full timeJob 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...
-
Study Site Management Expert
11 hours ago
kwai tsing district, Hong Kong SAR China IQVIA Argentina Full timeKey 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...
-
Clinical Research Associate
5 days ago
kwai tsing district, Hong Kong SAR China IQVIA Argentina Full timeAbout the JobWe are seeking a skilled Clinical Research Associate to join our team in IQVIA Argentina. As a key member of our site management team, you will be responsible for ensuring that clinical trials are conducted efficiently and effectively at study sites.Key ResponsibilitiesPerform monitoring visits at clinical trial sites to ensure compliance with...
-
Clinical Research Associate
7 days ago
kwai tsing district, Hong Kong SAR China IQVIA Argentina Full timeJob Overview Ensure the integrity of clinical trials by monitoring and managing site activities in accordance with contracted scope, regulatory requirements, and study protocols.Develop and implement site recruitment strategies to meet project objectives.Evaluate site performance, address quality issues, and provide regular updates on study progress.Key...
-
Site Activation Specialist
3 days ago
Kwai Tsing District, Hong Kong SAR China IQVIA Argentina Full timeJob 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;...
-
Site Activation Specialist
3 days ago
Kwai Tsing District, Hong Kong SAR China IQVIA Argentina Full timeAbout 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...
-
Project Manager
3 days ago
Kwai Tsing District, Hong Kong SAR China IQVIA Argentina Full timeJob 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...
-
Research Project Manager
2 days ago
kwai tsing district, Hong Kong SAR China IQVIA Argentina Full timeJob 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...
-
Research Coordinator
7 days ago
kwai tsing district, Hong Kong SAR China IQVIA Argentina Full timeJob SummaryIQVIA is seeking an experienced professional to manage and monitor clinical trial sites. The ideal candidate will have a strong understanding of clinical research regulations and protocols, as well as excellent communication and organizational skills.ResponsibilitiesSite management: Ensure sites are conducting the study in accordance with the...
-
Research Assistant
4 days ago
kwai tsing district, Hong Kong SAR China IQVIA Argentina Full timeAbout the RoleThe Clinical Research Associate will be responsible for ensuring the successful conduct of clinical trials at study sites in IQVIA Argentina. This role requires a high level of expertise in clinical research, strong communication and interpersonal skills, and the ability to work independently and collaboratively as part of a team.Key...
-
Regulatory Compliance Specialist
7 days ago
kwai tsing district, Hong Kong SAR China IQVIA Argentina Full timeJob Title: Regulatory Compliance SpecialistDescriptionThe successful candidate will be responsible for ensuring the integrity of clinical trials through effective site management and monitoring.Key Responsibilities:Conduct site monitoring visits to verify compliance with study protocols and regulations.Develop and implement site-specific recruitment plans to...
-
Clinical Trials Coordinator
2 days ago
kwai tsing district, Hong Kong SAR China IQVIA Argentina Full timeJob 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...
-
Clinical Research Associate
2 weeks ago
Kwai Tsing District, Hong Kong SAR China IQVIA Argentina Full timeJob 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...
-
Clinical Research Associate
17 hours ago
kwai tsing district, Hong Kong SAR China IQVIA Argentina Full timeJob 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...
-
Regulatory Compliance Specialist
7 hours ago
kwai tsing district, Hong Kong SAR China IQVIA Argentina Full timeAbout 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...
-
Clinical Research Associate Professional
15 hours ago
kwai tsing district, Hong Kong SAR China IQVIA Argentina Full timeJob 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.
-
Data Center Project Manager
2 days ago
kwai tsing district, Hong Kong SAR China DayOne Full timeJob 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...
-
Operations Manager
2 days ago
kwai tsing district, Hong Kong SAR China Hong Kong Ferry (Holdings) Company Limited Full timeJob Description We are seeking a dynamic and results-driven Production Manager (Business Improvement) to lead transformative initiatives within our production operations. The ideal candidate will be a strategic thinker with a proven track record in optimizing processes, driving continuous improvement, and fostering a high-performance culture.This role is...
-
Process Improvement Lead
2 days ago
kwai tsing district, Hong Kong SAR China Hong Kong Ferry (Holdings) Company Limited Full timeAbout Us Hong Kong Ferry (Holdings) Company Limited seeks a seasoned Production Manager (Business Improvement) to spearhead innovative initiatives that drive operational excellence and boost competitiveness.As a forward-thinking leader, you will orchestrate transformative projects to enhance production processes, streamline workflows, and eliminate waste....
-
Production Manager
2 weeks ago
Kwai Tsing District, Hong Kong SAR China Hong Kong Ferry (Holdings) Company Limited Full timeProduction Manager (Business Improvement)We are seeking a dynamic and results-driven Production Manager (Business Improvement) to lead transformative initiatives within our production operations. The ideal candidate will be a strategic thinker with a proven track record in optimizing processes, driving continuous improvement, and fostering a high-performance...