Durham, North Carolina, United States · On-site
$87k–$216k/yr
JOB OVERVIEW Performs and oversees the set-up of individual systems (EDC, IRT etc), ensuring data standards are followed leading to successful data integration with the Data Factory (DF)/Clinical Data Repository (CDR). E…
Skills: Clinical Data Management, Data Integration, EDC, IRT, Systems Integration Planning
Shanghai, Shanghai, China · On-site
Job Overview Provides high quality, timely development and on-time input to solutions for service delivery, managed services, or implementation oriented client projects. Assignments range in complexity from basic analysi…
Skills: Business Analysis, Technical Design, Project Management, Requirement Analysis, Quantitative Analysis
Zaventem, Flanders, Belgium · Remote OK
IQVIA is growing! Hiring multiple Clinical Data Management (CDM) Leads across our FSP (Functional Service Provider) and Traditional (Sponsor-Agnostic) delivery models. Apply now and have your resume considered for Lead D…
Skills: Clinical Data Management, Medidata Rave, Oracle InForm, GCP, ICH
Bloemfontein, Free State, South Africa · On-site
Internal Job Description PURPOSE Quality Reviewer RESPONSIBILITIES Conduct internal Data Management Quality Reviews in order to fulfil business unit, customer and regulatory authority requirements and expectations. Ensur…
Skills: Data Management Quality Review, CAPA, Medical Terminology, Clinical Trials Management, Regulatory Compliance
Kirkland, Quebec, Canada · On-site
$153k–$204k/yr
Conseiller principal, synthèse des données probantes PRÉSENTATION Les conseillers principaux sont des responsables de l’exécution de projets chargés de mettre en œuvre une recherche de synthèse des données probantes méth…
Skills: Systematic Literature Review, Indirect Treatment Comparison, Network Meta-Analysis, Matching-Adjusted Indirect Comparison, R
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 Relationship Management, First Level Support, Data Analysis, Market Analysis, Organization
Madrid, Community of Madrid, Spain · On-site
Te apasiona la venta y el contacto directo con farmacias? 🚀 ¿Eres un perfil claramente comercial y orientado a resultados? ¡Esta es tu oportunidad! Buscamos un/a Delegado/a de Ventas con experiencia en canal farmacia 💼…
Skills: Sales Management, Pharmacy Channel Experience, Negotiation, Customer Relationship Management, Business Development
Warsaw, Masovian Voivodeship, Poland · On-site
$151k–$281k/yr
Primary Function: Centralized Monitoring Lead (CML) partners with the Clinical Lead and local country Site Monitors in project execution. Provides centralized support to monitoring visits and site management for a variet…
Skills: Centralized Monitoring, Clinical Trial Conduct, ICH GCP, Risk Assessment, Data Trending
Buenos Aires, Argentina · On-site
The Regulatory and Start-Up Specialist will perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating proced…
Skills: Site Activation, Regulatory Affairs, Clinical Research, Document Management, Quality Control
Mannheim, Baden-Württemberg, Germany · On-site
IQVIA™ – The Human Data Science Company™ – ist ein führender, globaler Anbieter von zukunftsweisender Analytik, Technologielösungen und klinischer Auftragsforschung. IQVIA unterstützt Life Science Unternehmen, Verbände, …
Skills: Customer Orientation, Communication Skills, Gynaecology Knowledge, Women’s Health Expertise, CRM Systems
Bengaluru, Karnataka, India · On-site
Job Overview As a Senior Data Platforms SRE, you will serve as a technical escalation point and resolve higher complexity incidents and technical problems end to end. This role requires advanced troubleshooting expertise…
Skills: Advanced Troubleshooting, Incident Resolution, Data Platforms, Operational Discipline, Service Improvement
Mannheim, Baden-Württemberg, Germany · On-site
IQVIA™ – The Human Data Science Company™ – ist ein führender, globaler Anbieter von zukunftsweisender Analytik, Technologielösungen und klinischer Auftragsforschung. IQVIA unterstützt Life Science Unternehmen, Verbände, …
Skills: Pharmaceutical Sales, Customer Orientation, Compliance Knowledge, CRM Systems, Gynaecology Knowledge
Taguig, Metro Manila, Philippines · Hybrid
Roles and Responsibilities: Communicates with end users to clarify and define requirementsProvide comprehensive Customer/Technical support services to support center customersWork within Service Level AgreementsAbility t…
Skills: Customer Support, Technical Support, Clinical Experience, Medical Terminology, Critical Thinking
Istanbul, Istanbul, Turkey · 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: Clinical Research, Regulatory Compliance, Site Activation, Project Management, GCP
Parsippany, New Jersey, United States · On-site
$35/hr–$42/hr
Clinical Research Coordinator - Albuquerque, NM Work Set‑Up: On‑site Schedule: 24 Hours/Week (Part‑time) About IQVIA IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services. W…
Skills: Clinical Research Coordination, Patient Recruitment, GCP Guidelines, EDC Systems, Biological Sample Collection
São Paulo, São Paulo, Brazil · Hybrid
Under moderate supervision, the Regulatory and Start Up Specialist executes the feasibility, site identification regulatory, start-up, and maintenance activities in accordance with regulations, SOPs, and project requirem…
Skills: Regulatory Affairs, Site Activation, Feasibility Analysis, Contract Negotiation, Site Documentation
Sofia, Sofia-City, Bulgaria · On-site
Job Description Summary: Under appropriate guidance, ensure that personal administration and HR processes are executed in-country in full compliance with local labor legislation, Core HR standards, and corporate policies…
Skills: Personnel Administration, Labor Legislation, Employee Relations, Onboarding, HR Reporting
London, England, United Kingdom · Remote OK
$34k–$61k/yr
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, GCP/ICH Guidelines, Clinical Research, Contract Management
Zaventem, Flanders, Belgium · Remote OK
IQVIA is growing! Hiring multiple Clinical Data Management (CDM) Leads across our FSP (Functional Service Provider) and Traditional (Sponsor-Agnostic) delivery models. Apply now and have your resume considered for Lead D…
Skills: Clinical Data Management, Study Setup, Database Lock, EDC Systems, Medidata Rave
Gurugram, Haryana, India · On-site
IQVIA™ is The Human Data Science Company™, combining data, technology, advanced analytics, and human expertise to help healthcare clients improve outcomes for patients. Our solutions support better decision-making across…
Skills: Project Management, Stakeholder Management, Quantitative Analysis, Qualitative Analysis, Strategy Consulting
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Oversees the setup of clinical systems like EDC and IRT to ensure successful data integration with the Data Factory and Clinical Data Repository. Guides project teams on optimal data flow design patterns to enable real-time alerts and analytics.
Requires a Bachelor's degree in Science, Computer Science, or IT with 8-10 years of experience, including at least 7 years in a CRO environment. Must possess strong analytical skills and deep knowledge of clinical systems and data flow paths.
JOB OVERVIEW
Performs and oversees the set-up of individual systems (EDC, IRT etc), ensuring data standards are followed leading to successful data integration with the Data Factory (DF)/Clinical Data Repository (CDR). Ensure the data collected and integrated into the Data Factory (DF)/Clinical Data Repository (CDR), can be successfully utilized in all downstream systems by First Patient In (FPI).
RESPONSIBILITIES
• Work directly with project teams to guide/convey optimal data flow design patterns across the enterprise consisting of multiple systems with the end goal to ensure data integrations enable real time Alerts and Analytics
• Lead vendor data set-up for Data Management vendors and other functions as required, enabling the data flow for downstream activities (data cleaning, etc).
• Complete and manage the 'Systems Integration Plan' to detail the data flow and highlight potential risks/challenges while collaborating with various groups (i.e. IPA, Study Team, CDAT) to provide data standardization and alignment of site visits across systems”.
• Champion people, process and technology improvements and standards to enhance quality, increase productivity (internal and external with Investigator sites) and reduce data latency within Quintiles clinical trial systems inclusive of IVxS, EDC, CTMS, QRPM, Data Factory, Triggers and Alerts, Visualizations such as Clinical Analytics and Federated reports, CDOS and SLDRs.
• Guide and present study teams with best case options given limitations (e.g. contract, cost, timelines, etc.) with the ability to articulate pros and cons of each approach.
• Identify and implement innovative solutions to challenges and influence future decision-making in order to reduce workarounds.
• Review data transfers specifications to ensure they meet the standards required to develop quality data integrations.
• Proactively provide education and training to ensure adherence of the relevant startup SOPs and best practices during the RFI and post-award phases.
• Collaborate with the global IT organization as needed to resolve support issues related to data integration or data quality.
• Ability holistically understands the process and structure of 5-10 individual systems and determine how the design of one system may impact the ability of another system to function optimally.
REQUIRED KNOWLEDGE, SKILLS AND ABILITIES
Experience working in Drug Discovery, clinical trial conduct, clinical data management or related industries.
Excellent critical thinking and analytical skills, strong attention to detail
Effective written, interpersonal, and verbal communication skills
Strong influencing, problem resolution, motivation, and negotiation skills
Solution-oriented approach to challenges
Sound leadership and customer service skills
Competent presentation skills meeting the needs of all levels
Ability to establish and maintain effective working relationships with team members, management, operations staff, clients, and executive management
Ability to lead effective meetings
Strong organizational and time management skills
Ability to manage multiple dependencies across multiple systems to reach a final deliverable
Ability to establish and maintain effective working relationships with teams involved in study start up
MINIMUM EXPERIENCE
Bachelor in Science/Computer Science/Information Technology or Bachelor in Technology with 8 to 10 years experience OR equivalent combination of education and experience.
7+ years of CRO experience with knowledge of clinical systems, the data points stored within them and data flow paths.
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 proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe
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.
The potential base pay range for this role, when annualized, is $86,500.00 - $216,000.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.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
