Taguig, Metro Manila, Philippines · On-site
Role Purpose: Responsible for the daily maintenance of healthcare Organizations and Prescribers in all database of the US Region. Validates, research & analyses to client data inquiries with the use of the process tool. …
Skills: Data Maintenance, Data Validation, Research, Outbound Phone Verification, Data Analysis
Bucharest, Romania · Remote Solely
Job Overview Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requiremen…
Skills: Site Activation, Regulatory Submissions, ICF Adaptation, GCP/ICH Guidelines, Clinical Research
Beijing, Beijing, China · On-site
Essential Functions • Manage staff in accordance with organization’s policies and applicable regulations. Responsibilities include planning, assigning, and directing work, assessing performance and guiding professional d…
Skills: Staff Management, Clinical Trial Management, GCP, ICH Guidelines, Resource Allocation
Beijing, Beijing, China · On-site
Essential Functions • Manage assigned sites and perform Subject Level Data Review independently, if required perform with both responsibilities as dual role.; • Perform remote monitoring visits for assigned sites as assi…
Skills: Subject Level Data Review, Remote Monitoring, Clinical Trial Conduct, ICH GCP, Trend Analysis
São Paulo, São Paulo, Brazil · On-site
Job Overview Under general supervision, perform tasks at a country level associated with site activation activities in accordance with applicable local and/or international regulations, standard operating procedures (SOP…
Skills: Contract Negotiation, Clinical Trial Agreements, Site Activation, Budget Negotiation, Regulatory Compliance
Shanghai, Shanghai, China · On-site
Job Overview Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. Essential Functi…
Skills: Administrative Support, Trial Master File Management, Clinical Documentation, Microsoft Word, Microsoft Excel
Beijing, Beijing, China · On-site
• Under general supervision, serve as Single Point of Contact (SPOC) in assigned studies for investigative sites, Site Activation Manager (SAM), Project Management team, and other departments as necessary. Ensure adheren…
Skills: Site Activation, Clinical Research, Regulatory Documentation, Feasibility Analysis, Quality Control
São Paulo, São Paulo, Brazil · Hybrid
Sobre a IQVIA: A IQVIA é líder global em Human Data Science, oferecendo soluções integradas de pesquisa clínica, informação e tecnologia para o setor de saúde. Combinando dados, expertise analítica e inovação, apoiamos n…
Skills: Customer Service, Client Relationship Management, Data Analysis, Microsoft Excel, Microsoft PowerPoint
São Paulo, São Paulo, Brazil · On-site
Essa vaga é exclusiva para Pessoas com Deficiência. Controlar e conciliar despesas do cartão corporativo, garantindo conformidade com as políticas internas;Realizar lançamentos contábeis e classificações de despesas no s…
Skills: Corporate Card Reconciliation, Accounting Entries, Expense Classification, Corporate Travel Coordination, Vendor Management
Santa Clarita, California, United States · On-site
$59k–$123k/yr
We are seeking an Associate Manager, Flow Cytometry to join IQVIA Laboratories on site at Valencia. We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want t…
Skills: Flow Cytometry, Laboratory Operations, Staff Supervision, CAP/CLIA Compliance, Quality Control
Durham, North Carolina, United States · On-site
$57k–$143k/yr
Job Overview Manage the operational aspects of projects and programs. Will ensure that all project work is completed in accordance with SOPs, policies and practices. Essential Functions • Create, track and report on proj…
Skills: Project Management, Financial Reporting, Budget Management, Interactive Response Technology (IRT), Cross-functional Coordination
New Providence, New Jersey, United States · On-site
$54k–$135k/yr
Job Overview The Vendor Compliance Lead for Patient Support Services (PASS) is responsible for ensuring all vendors supporting the commercial Patient Access & Support Services business operate in full compliance with IQV…
Skills: Vendor Management, Risk Management, Procurement Workflows, Quality Assurance Auditing, Compliance Frameworks
Shanghai, Shanghai, China · On-site
Essential Functions • Under general supervision, serve as Single Point of Contact (SPOC) in assigned studies for investigative sites, Site Activation Manager (SAM), Project Management team, and other departments as neces…
Skills: Site Activation, Clinical Research, Regulatory Documentation, Project Management, Quality Control
Shanghai, Shanghai, China · On-site
Job Overview Provides administrative and/or technical support. Recruitment Process 第一轮：线上测评 完成指定的线上测试，用于初步筛选。第二轮：业务面试 与业务部门进行面谈，深入了解您的专业背景与职位匹配度。第三轮：结果通知 招聘团队将在流程结束后，正式告知最终结果。 Essential Functions • Responsible to reconci…
Skills: SAP, Financial Reconciliation, Journal Entries, Data Analysis, SharePoint
Taipei, Taiwan · On-site
Position Summary The SEAT (Southeast Asia and Taiwan) Rare Diseases Lead directly reports to Senior Director, Rare Diseases EU & Int'l, Global Rare Diseases Business Unit. The function leads the full spectrum of activiti…
Skills: Rare Disease Commercialization, Market Access, Brand Planning, Sales Management, KOL Management
Shanghai, Shanghai, China · On-site
Job Overview Develop and prepare contracts and budgets for assigned customers, to support the global sales team. Essential Functions • Work closely with project teams to determine appropriate terms and conditions of cont…
Skills: Contract Development, Budget Preparation, Project Management, Customer Relationship Management, Written Communication
Shanghai, Shanghai, China · On-site
Job Overview Provides administrative and/or technical support. Recruitment Process 第一轮：线上测评 完成指定的线上测试，用于初步筛选。 第二轮：业务面试 与业务部门进行面谈，深入了解您的专业背景与职位匹配度。 第三轮：结果通知 招聘团队将在流程结束后，正式告知最终结果。 Essential Functions • Responsible to recon…
Skills: SAP, Financial Reconciliation, Journal Entries, Data Analysis, SharePoint
Milan, Lombardy, Italy · On-site
$48k–$71k/yr
Plan and conduct independent clinical (GCP) audits to assess compliance with regulations, guidelines, and operating procedures. Prepare and distribute reports of findings to supervisor, operations staff, management, and …
Skills: GCP Auditing, Clinical Trial Audits, CAPA Management, Root Cause Analysis, Regulatory Compliance
Remote Solely
JOB OVERVIEW Do you have a keen eye for detail and a passion for ensuring the accuracy and clarity of medical documents? We’re on the hunt for skilled Freelance regulatory affairs translators (English into Icelandic) to …
Skills: English to Icelandic Translation, Regulatory Affairs Translation, Medical Translation, Post-editing, CAT Tools
Warsaw, Masovian Voivodeship, Poland · Remote OK
Job Overview The Medical Director for the Hematology-Oncology Center of Excellence provides strategic medical and scientific subject matter input to IQVIA in this therapeutic area informed by their training, experience a…
Skills: Oncology, Hematology, Clinical Development Planning, Protocol Design, Bid Defense
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Responsible for the daily maintenance and validation of healthcare organization and prescriber databases for the US region. This involves conducting research via internet searches and phone verifications to ensure data accuracy and completeness.
Requires a high school diploma or equivalent with basic proficiency in Windows applications like Excel and Word. Candidates must possess strong communication skills, critical thinking abilities, and a willingness to work night shifts.
Responsible for the daily maintenance of healthcare Organizations and Prescribers in all database of the US Region.
Validates, research & analyses to client data inquiries with the use of the process tool.
Complete maintenance of reference data (healthcare Organizations and Prescribers) as essential for US Production.
Perform research such as Internet Search, Phone Verification, Database Matches and etc. to gather information from third parties that will validate the completeness or accuracy of the data.
Perform outbound phone verification of details on Organization and Prescriber records to validate accuracy of reference data maintained as well as capture client-required details such as primary office address and primary profession/specialty.
Performs ad hoc data analysis and participates on various process improvement as needed.
Validate that the information gathered from third-party sources represents accurate new data that should result in an update, creation, or deletion in the database existing data.
High School Diploma or equivalent Req
Experience in handling voice and healthcare account is an advantage but not a requirement.
Basic knowledge in Windows applications (Excel, Word).
Strong verbal and / or written communication skills in either the language of the country supplied or English.
Critical thinking and problem-solving skills.
Demonstrate strong understanding of complex concepts and processes.
Has initiative and is self-motivated to see through until resolution concerns raised by Clients.
Candidate must be willing to work in night.
IQVIA 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 to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
IQVIA (NYSE:IQV) is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. IQVIA’s portfolio of solutions are powered by IQVIA Connected Intelligence™ to deliver actionable insights and services built on high-quality health data, Healthcare-grade AI™, advanced analytics, the latest technologies and extensive domain expertise. With approximately 88,000 employees in over 100 countries, including experts in healthcare, life sciences, data science, technology and operational excellence, IQVIA is dedicated to accelerating the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. IQVIA is a global leader in protecting individual patient privacy. The company uses a wide variety of privacy-enhancing technologies and safeguards to protect individual privacy while generating and analyzing information on a scale that helps healthcare stakeholders identify disease patterns and correlate with the precise treatment path and therapy needed for better outcomes. IQVIA’s insights and execution capabilities help biotech, medical device and pharmaceutical companies, medical researchers, government agencies, payers and other healthcare stakeholders tap into a deeper understanding of diseases, human behaviors and scientific progress, in an effort to advance healthcare. To learn more, visit www.iqvia.com.
Offices: 2400 Ellis Rd, Durham, North Carolina 27703, US
IQVIA (NYSE:IQV) is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. IQVIA’s portfolio of solutions are powered by IQVIA Connected Intelligence™ to deliver actionable insights and services built on high-quality health data, Healthcare-grade AI™, advanced analytics, the latest technologies and extensive domain expertise. With approximately 88,000 employees in over 100 countries, including experts in healthcare, life sciences, data science, technology and operational excellence, IQVIA is dedicated to accelerating the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. IQVIA is a global leader in protecting individual patient privacy. The company uses a wide variety of privacy-enhancing technologies and safeguards to protect individual privacy while generating and analyzing information on a scale that helps healthcare stakeholders identify disease patterns and correlate with the precise treatment path and therapy needed for better outcomes. IQVIA’s insights and execution capabilities help biotech, medical device and pharmaceutical companies, medical researchers, government agencies, payers and other healthcare stakeholders tap into a deeper understanding of diseases, human behaviors and scientific progress, in an effort to advance healthcare. To learn more, visit www.iqvia.com.
Offices: 2400 Ellis Rd, Durham, North Carolina 27703, US
