Manila, Metro Manila, Philippines · On-site
Essential Functions • Resource Headcount management including existing, attrition and new hire. Analysis versus Budget and Forecast on a monthly basis • Track joiners moving into / out of teams and ensure profiles creati…
Skills: Resource management, Headcount management, Data analysis, Project scheduling, Advanced Excel
Netanya, Center District, Israel · On-site
Study Start Up Clinical Research Associate IQVIA is looking for talented and motivated team member to join our Sponsor dedicated team as Study Start Up Clinical Research Associate. At this position you would be responsib…
Skills: Clinical Research, Study Start-up, Site Selection, Regulatory Submissions, Good Clinical Practice
Kochi, Kerala, India · On-site
Job Overview Conduct testing activities in CDMS environment and provide comprehensive testing expertise to the team to produce efficient, quality database that meets customer requirements. Essential Functions • Independe…
Skills: Clinical Database Testing, CDMS, InForm, RAVE, OCRDC
Sydney, New South Wales, Australia · On-site
Dermatology Clinical Trials | Liverpool NSW | Immediate Start IQVIA is seeking two experienced Registered Nurses to support clinical research activities at a clinical trial site based in Liverpool, NSW. This is an excell…
Skills: Clinical research, Dermatology, Registered nurse, Good clinical practice, Venepuncture
Taguig, Metro Manila, Philippines · On-site
ROLE PURPOSE: • Responsible for daily maintenance of pharmaceutical products in all the database of the US. • Perform analysis, bridging & resolution of the products database exceptions for internal and external communic…
Skills: Pharmaceutical product maintenance, Data analysis, Database integrity, Problem solving, Business analytical skills
Netanya, Center District, Israel · 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: Clinical Research, Trial Master File, Administrative Support, Regulatory Compliance, Clinical Documentation
Shinjuku, Japan · Hybrid
Overview 3-4日のリモート勤務可能QMS関連のコンサルティング業務を担当する機会があります。 To understand requirements from QMS/PMD Act., and support QA Senior Manager who drive forward proper Quality Management system operation and maintenance Create document…
Skills: Quality Assurance, QMS, PMD Act, Regulatory Affairs, Medical Device
Shanghai, Shanghai, China · On-site
Job Overview Provide legal advice and services to support the organization’s business in assigned region, in one or more of the following areas: contract law, employment law, commercial law, regulatory or compliance. May…
Skills: Contract Law, Employment Law, Commercial Law, Regulatory Compliance, Contract Negotiation
Manila, Metro Manila, Philippines · Remote OK
IQVIA™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a b…
Skills: Project coordination, Administrative support, Event management, Data analysis, Financial reconciliation
Beijing, Beijing, China · On-site
工作职责 1.协助完成实习生招聘全流程，包括简历筛选、面试安排及录用跟进，保障招聘效率。 2. 负责招聘系统的简历信息维护与数据更新，确保人才库的准确性与完整性。 3. 参与内部推荐活动的物料制作，如设计宣传文案、制作PPT等，提升招聘渠道影响力。 4. 整理并制作各类人事表格，完成员工信息归档与数据统计工作。 5. 配合部门同事完成其他人力资源相关事务性工作，支持团队日常运营。 任职要求 1.本科及以上学历，2027届毕业生，人力资源…
Skills: Recruitment, Resume Screening, Interview Coordination, Data Entry, Microsoft Excel
Taguig, Metro Manila, Philippines · On-site
Job Overview Provide financial and operational support for business projects and activities, ensuring accurate and timely execution of financial processes, compliance with company policies and audit requirements, effecti…
Skills: Financial analysis, Revenue recognition, Variance analysis, Excel, Pivot tables
Buenos Aires, Argentina · On-site
Job Overview Engage in structured training program to gain knowledge and skills required to independently conduct clinical monitoring visits in accordance with study protocol, standard operating procedures, good clinical…
Skills: Clinical monitoring, Good clinical practice, Regulatory compliance, Site management, Protocol training
Beijing, Beijing, 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, Excel, Data reconciliation, Journal entries, Vendor database maintenance
Netanya, Center District, Israel · On-site
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 r…
Skills: Clinical Research, Site Monitoring, Good Clinical Practice, GCP, ICH Guidelines
Taguig, Metro Manila, Philippines · On-site
Job Overview Under broad guidance, ensures clients obtain maximum value from products and services in order to facilitate a positive and productive long-term relationship, either broad client or offering focused. Essenti…
Skills: Data analysis, Reporting, Client-facing, Data presentation, Microsoft Excel
Taguig, Metro Manila, Philippines · On-site
Job Overview The FMV Analyst is part of the team that provides detailed wage data and related consulting to client- based on industry information. The FMV Analyst provides high quality, on-time input to client projects i…
Skills: Data analysis, Reporting, Microsoft Excel, Power BI, Power Query
Beijing, Beijing, China · On-site
工作职责： 1. 作为研究团队成员，遵照法规要求、商定的工作范围、适用的SOP、工作授权和试验方案，在研究中心进行工作。 2.协助研究者完成可行性调查问卷和回收问卷。 3.推动研究中心启动工作：协助研究中心筛选访视，协助及时提交文件到伦理委员会进行审批和试验用药品的发放，协助研究中心启动访视。 4.协助研究者进行受试者筛选和入组研究。 5.得到研究者授权后，根据法规和GCP的要求，协助研究者顺利完成方案要求的随访和步骤：如制定计划、清点…
Skills: Clinical research, GCP compliance, Medical terminology, Data entry, Regulatory compliance
Manila, Metro Manila, Philippines · On-site
The Role You will be responsible for coordinating and managing linguistic validation and eCOA projects from start to completion in accordance with IQVIA SOPs. Your Responsibilities will include: Managing multiple transla…
Skills: Project management, Linguistic validation, ECOA, Translation management, Localization
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 management, Budgeting, Project management, Customer relationship management, Written communication
Beijing, Beijing, China · On-site
requests and studies, including oversight of technical processes and procedures insofar as they impact pathology interpretations. Perform microscopic analyses of laboratory assays and monitor digitization of slides. Corr…
Skills: Anatomic pathology, Immunohistochemistry, FISH, Cytogenetics, Histopathology
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The specialist will manage resource headcount, track project assignments, and maintain data accuracy across enterprise tools. They are also responsible for generating dashboards and reports related to utilization, compliance, and resource availability.
Candidates must have 3-6 years of experience in business operations or resource management, preferably within a life sciences or pharma environment. Proficiency in advanced Excel and enterprise resource management applications is mandatory.
Essential Functions
• Resource Headcount management including existing, attrition and new hire. Analysis versus Budget and Forecast on a monthly basis
• Track joiners moving into / out of teams and ensure profiles creation in enterprise tools of the organization
• Maintain and upkeep of data related to resources (Rate card, Utilization targets, team/product related information)
• Planning and executing periodic Skills assessment process – reporting progress and reporting / analytics of Skills data
• Update and maintain resource project assignments and schedules on enterprise tools
• Tracking resource bandwidth/availability using excel and enterprise tools. Work with Resource managers and Line managers through regular cadence on data validity and accuracy
• Standard/ad-hoc reports and dashboards related to headcount, utilization, compliance and Availability
• Contractors’ extension tracking
• Follow up and tracking of non-billable hours’ analysis and reporting to management
Experience & Qualifications
• Graduate in Sciences, Commerce or Engineering subjects
• 3-6 years of Business Operations/PMO/Resource management experience in a MNC company, with exposure to Technology, Analytics, Data Management skills, projects and methodologies. Experience in a Life Sciences/Pharma company is an advantage
• Experience in using HR/Finance/Resource Management enterprise applications is a must. Salesforce knowledge, specifically CRM and PSA, is a definite plus
• Excellent written and verbal communication in English is mandatory
• Advanced Excel skills is mandatory. Should have proficiency in Outlook, PowerPoint, Word and other Microsoft Office applications
• Should have experience in using SharePoint, OneNote and TEAMS
• Problem solving and logical reasoning skills are a must
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
