IQVIA

Lead, manage and provide support to a team of Centralised Monitoring project coordinators (CPCs) in the management of the assigned activities. Manage staff according to the organization’s policies and applicable regulations Essential Functions This position requires a combination of Technical Skills like managing and assigning centralized monitoring activities and responsibilities (moderate to complex protocols/ non-protocol tasks) competently with 1+ years of direct line manager experience The candidate needs to be based out of Kochi and should operate from office all 5 days of the week. Need a strong dynamic lead from Clinical background for this position, given that he/she will be assigned the responsibility to lead this site. Education: Life-science background Exp: 5+ years of relevant work experience Should have experience in People Managing role in Hospital or Lab background   Lead, manage and provide support to a team of Centralized Monitoring project coordinators (CPCs) in the management of the assigned activities. Manage staff according to the organization’s policies and applicable regulations• Planning, assigning, and directing work, mentoring and assist in training of CPCs. Appraising performance and guiding professional development• rewarding and disciplining employees• addressing employee relations issues and resolving problems. Approve actions on human resources matters.• Establish a close working relationship with the global project team, operational teams and appropriate counterparts to ensure consistent quality, global delivery, productivity of all studies which may include sponsor specific standards and procedures.• Participate in the selection and on boarding process for new staff, conduct candidate review and interviews. Conduct on boarding training for new staff in conjunction with Human Resources and Global Talent training programs.• Ensure that the staff has proper materials, systems access and training to complete job responsibilities. Provide oversight for the execution of the training plan, SOP review and mentored training experiences, as applicable.• Participate in assigning staff to studies that are appropriate to their experience and training, track assignment of the staff to projects and report relevant metrics to management• Track staff output quality by conducting regular mini audits.• Participate and lead in investigation on quality incidents including root cause analysis, and identification of a robust CAPA plan.• Identify risks and issues and create appropriate corrective action plans to prevent or correct deficiencies in performance of staff.• Regularly track metrics as agreed with management for individual staff and the department• Participate in continuous improvement programs at a departmental level to ensure excellent service delivery and quality focus. Qualifications• High School Diploma or equivalent• 5-8 Years.• 5  relevant experience and/or equivalent combination of education, training and experience. 1-2 years relevant experience in line management.• 1)    In-depth knowledge of and skill in applying, applicable clinical research regulatory requirements.• i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.• 2)    Basic therapeutic and protocol knowledge.• 3)    Excellent written and verbal communication and interpersonal skills, including good command of English language and strong leadership skills.• 4)    Excellent organizational and problem solving skills.• effective time management skills and ability to manage competing priorities.• 5)    Strong ability to establish and maintain effective working relationships with coworkers and managers.• 6)    Excellent customer service skills.• good presentation skills.• 7)    Strong software and computer skills, including MS Office applications and maintain effective working relationships with coworkers, managers and clients. Job OverviewLead, manage and provide support to a team of Centralised Monitoring project coordinators (CPCs) in the management of the assigned activities. Manage staff according to the organization’s policies and applicable regulations Essential Functions• Lead, manage and provide support to a team of Centralized Monitoring project coordinators (CPCs) in the management of the assigned activities. Manage staff according to the organization’s policies and applicable regulations• Planning, assigning, and directing work, mentoring and assist in training of CPCs. Appraising performance and guiding professional development• rewarding and disciplining employees• addressing employee relations issues and resolving problems. Approve actions on human resources matters.• Establish a close working relationship with the global project team, operational teams and appropriate counterparts to ensure consistent quality, global delivery, productivity of all studies which may include sponsor specific standards and procedures.• Participate in the selection and on boarding process for new staff, conduct candidate review and interviews. Conduct on boarding training for new staff in conjunction with Human Resources and Global Talent training programs.• Ensure that the staff has proper materials, systems access and training to complete job responsibilities. Provide oversight for the execution of the training plan, SOP review and mentored training experiences, as applicable.• Participate in assigning staff to studies that are appropriate to their experience and training, track assignment of the staff to projects and report relevant metrics to management• Track staff output quality by conducting regular mini audits.• Participate and lead in investigation on quality incidents including root cause analysis, and identification of a robust CAPA plan.• Identify risks and issues and create appropriate corrective action plans to prevent or correct deficiencies in performance of staff.• Regularly track metrics as agreed with management for individual staff and the department• Participate in continuous improvement programs at a departmental level to ensure excellent service delivery and quality focus. Qualifications• High School Diploma or equivalent• 5-8 Years.• 5+  relevant experience and/or equivalent combination of education, training and experience. 1-2 years relevant experience in line management.• 1)    In-depth knowledge of and skill in applying, applicable clinical research regulatory requirements.• i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.• 2)    Basic therapeutic and protocol knowledge.• 3)    Excellent written and verbal communication and interpersonal skills, including good command of English language and strong leadership skills.• 4)    Excellent organizational and problem solving skills.• effective time management skills and ability to manage competing priorities.• 5)    Strong ability to establish and maintain effective working relationships with coworkers and managers.• 6)    Excellent customer service skills.• good presentation skills.• 7)    Strong software and computer skills, including MS Office applications and maintain effective working relationships with coworkers, managers and clients. 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.

Job OverviewWe are looking for a Senior QA Engineer with strong hands-on experience in manual testing and a basic understanding of automation. The role involves validating applications, ensuring quality standards, and supporting overall test strategy in an Agile environment.Key ResponsibilitiesAnalyze business and functional requirements to create effective test scenarios and test cases.Execute manual testing, including functional, regression, and API testing (e.g., Postman).Conduct database testing using SQL (MySQL, Redshift, or Snowflake).Identify, log, and track defects through to resolution.Contribute to test plans, test strategy, and QA documentation.Work closely with cross-functional teams in Agile/Scrum setups.Support and mentor junior QA team members.Continuously suggest improvements to QA processes and quality standards.Requirements4+ years of experience in QA, primarily in manual testing.Strong understanding of SDLC and STLC.Hands-on experience with API testing and database validation.Exposure to cloud platforms (AWS or Azure).Good to HaveKnowledge of automation tools such as Selenium, Katalon Studio, or Playwright.Basic understanding of test automation frameworks.Exposure to performance testing tools like JMeter.Familiarity with AI-based testing tools or QA process improvements.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.

To lead Local Study Teams (LSTs) at country level to deliver committed components of clinical studies according to agreed resources, budget and timelines complying with Sponsor Procedural Documents, international guidelines such as ICH-GCP as well as relevant local regulations. In addition to leading LST(s), the Local Study Associate Director may perform site monitoring as needed to support the flexible capacity model.The Local Study Associate Director is responsible to ensure that sites are identified, site qualifications performed, set up, initiated, monitored, closed and documentation archived.MAIN RESPONSIBILITIESHas the overall responsibility for the study commitments within the country and for timely delivery of data to required quality.As per request can support as Lead CRA/ local study team leader.Optimizes the performance of the Local Study Teams at country level ensuring compliance with Sponsor Procedural Documents, ICH-GCP and local regulations.Ensures, as required, that clinical and operational feasibility assessment of potential studies is performed to the highest quality.Coordinates the site selection process by identifying potential sites/investigators, performing initial Site Quality Risk Assessment, and conducting Site Qualification Visits to evaluate suitability and quality risks.Ensures timely submission of application/documents to EC/IRB at start up and for the duration of the study. Works together with Regulatory Affairs to ensure timely delivery of application/documents for submissions to Regulatory Authority for the duration of the study, and in line with local regulations.Ensures timely preparation of country financial Study Management Agreement (fSMA) and maintains accurate study budget in Sponsor clinical studies financial system by regular checks of the system and financial reports (as agreed with Director, SMM/ Director, Country Head.Ensures timely preparation of local Master CSA (including site budget) and amendments as needed.Ensures timely preparation of country level Master Informed Consent Form (MICF) and subsequent site level ICFs, as required, including any relevant translations, and in line with relevant Sponsor SOPs and local regulations.Ensures all country and site level trial essential documents required by ICH-GCP prior to study start have been collected and verified for correctness, prior to setting sites ready to enrol, and in line with Sponsor SOPs.Plans and coordinates applicable local drug activities (from local purchase or reimbursement to drug destruction).Sets up and maintains the study in CTMS at study country level as well as local websites as required by local laws and regulations.Oversees, manages and coordinates monitoring activities from site activation through to study closure at country and site level in accordance with the Monitoring Plans.Reviews monitoring visit reports (as required and following Sponsor SOPs) and pro-actively advices the monitor(s) on study related matters.Performs any required co-monitoring, Accompanied Site Visits/training visits with study CRAs.Proactively identifies risks and facilitates resolution of complex study problems and issues.Organizes regular Local Study Team meetings on an agenda driven basis.Actively works towards achieving good personal relationships with all Local Study Team members, sites’ staff and global stakeholders.Reports study progress/update to the Global Study Associate Director/ Global Study Team including SMM Lead.Contributes to patient recruitment strategy including regular communication with participating Investigators as necessary.Develops, maintains and reviews risk management plan on country study level: proactively manages sites, stakeholders, local and global vendors and customers to ensure risks are timely identified, mitigated and managed.Communicates and co-ordinates regularly with National Co-ordinating Investigator / National Lead Investigator on recruitment and other study matters, if applicable.Plans and leads National Investigator meet Ensures that all study documents are ready for final archiving and completion of local part of the eTMF.Provides regular information to Line Managers at country level on study and planned study milestones/key issues.Updates Line Managers about the performance of the CRAs/CSAs.Ensures that study activities at country level comply with local policies and code of ethics.Provides feedback on any research related information including sites/investigators/competing studies that might be useful for the local market.Ensures compliance with Sponsor´s Code of Ethics, company policies and procedures relating to people, finance, technology, security and SHE (Safety, Health and Environment).Supports SMM in different initiatives (local, regional or global) as agreed with the SMM Line Management.REQUIRED SKILLS AND QUALIFICATIONSBachelor degree in related Life Science discipline.Minimum 3 years of experience in Clinical Monitoring (CRA, Sr CRA).Good knowledge of international guidelines ICH GCP as well as relevant local regulations.Proven ability to lead and motivate cross functional teams to deliver clinical trials according to or ahead of time plan, budget and with required quality.Good medical knowledge of Oncology therapeutic area.Excellent understanding of the Clinical Study Process including monitoring.Very good understanding of the Study Drug Handling Process and the Data Management Process.Excellent project management skills.Excellent ability to prioritize and handle multiple tasks, attention to details and negotiation skills.Excellent knowledge of spoken and written English and Turkish language.Good ability to learn and to adapt to work with IT systems.Proven ability to work independently with tasks allocated (as per request can support as Lead CRA/ local study team leader).Readiness to work in hybrid model with regular visits (2 - 3 days per week) at Sponsor's office in Istanbul.Please note: due to sponsor requirements for the role only candidates based in the listed location/s will be considered. Any applications from candidates based outside of these locations will not be considered.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.

Job OverviewProvide experienced technical expertise to develop process methodology for department to meet internal and external clients’ needs. Plan and coordinate the development of integrated programming solutions serving the full spectrum of statistical programming needs. Provide technical expertise and leadership to the department. Provide internal consulting services, including specifications and user needs analysis for complex project or client requirements. Essential Functions• Perform, plan and co-ordinate the following for complex studies: (i) the programming, testing, and documentation of statistical programs for use in creating statistical tables, figures, and listing summaries and (ii) the programming of analysis databases (derived datasets) and transfers of data for internal and external clients. May perform and plan the programming of database quality control checks.• Program and plan the integration of databases from multiple studies or sources.• Develop and co-ordinate programming documentation including plans and specifications, as appropriate, for complex studies.• Provide advanced technical expertise in conjunction with internal and external clients, and independently bring project solutions to teams and department, for complex studies.• Perform, plan and co-ordinate the development, implementation and validation of new process technologies, macros and applications.• Fulfill project responsibilities at the level of statstical team lead for single complex studies or group of studies.• Understand the Scope of Work, budget and quote assumptions, estimate the work completed, manage Out of Scope and resource forecasts for single studies. May manage project budget and resource requirements, and provide revenue forecasts for single studies.• Provide training and guidance to lower level staff. Qualifications• Master's Degree Computer science or related field and 3 years relevant experience Req Or• Bachelor's Degree Computer science or related field and 4 years relevant experience Req• Equivalent combination of education, training and experience in lieu of degree Req• Knowledge of statistics, programming and/or clinical drug development process• Advanced knowledge of computing applications such as Base SAS, SAS Graph and SAS Macro Language• Good organizational, interpersonal, leadership and communication skills• Ability to effectively manage multiple tasks and projects• Excellent accuracy and attention to detail• Ability to establish and maintain effective working relationships with coworkers, managers and clients 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.

Associate Principal / Principal, Clinical Outcome Assessment (COA) Strategy Consulting IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics, and human ingenuity to drive healthcare forward.  The Patient Centered Solutions team (PCS) The PCS team leads the industry in the science of measuring the patient experience. We pair strategic consulting expertise with technical scientific knowledge to design and execute scientifically rigorous research that incorporates the patient voice into the development and commercialization of new medicines. This research includes qualitative (e.g., patient interviews, focus groups), quantitative (e.g., clinical outcome assessments (COAs)/patient-reported outcomes (PROs), preference research) and passive (e.g., digital health technology tools) approaches to understand patient, caregiver and physician experiences and expectations of disease and treatment.  Why join? Become part of a recognized global leader in patient-focused researchKeep growing with an organization that encourages and invests in continuous professional and personal developmentApply your business and leadership skills in an entrepreneurial and multi-disciplinary teamContinue challenging yourself by addressing the toughest client issues, working across multiple geographies and solutions in a dynamic and crucial field for the industryMake a difference to patients by enabling the successful approval or launch of new treatments with features that are truly patient-centricResponsibilities The Associate Principal/ Principal Clinical Outcome Assessment (COA) Endpoint Strategy serves as the subject matter expert for COA endpoint strategy, endpoint development, COA regulatory strategy, and COA instrument science in client engagement and project delivery. This role brings deep expertise in COA measurement science to differentiate client solutions through expert-driven, highly insightful endpoint strategies. The role acts as a trusted advisor to pharmaceutical and biotechnology sponsors and represents IQVIA as an external scientific thought leader while ensuring internal scientific quality and best practices. Key responsibilities include: Client Strategy Leadership & Scientific Differentiation Develop COA endpoint strategies across clinical development programs, including primary and key secondary endpoint positioning in consulting projects.Bring COA expertise into client meetings, workshops, and strategic discussions.Differentiate proposals and client solutions through expert-driven COA strategy narratives.Translate emerging scientific and regulatory expectations into actionable client recommendations. Regulatory-Grade Endpoint Strategy & FDA Engagement  Advise sponsors on development and justification of COA endpoint strategies for regulatory interactions. Support preparation for and participation in FDA meetings as the COA subject matter expert. Guide sponsors on evidence expectations, context of use, and fit-for-purpose COA strategies. COA Instrument Development Leadership  Provide scientific leadership in the development of new COA instruments from concept to validation-ready tools. Lead and advise on drafting and refinement of COA instrument items, response options, recall periods, and scoring approaches. Oversee qualitative research activities supporting content validity, including concept elicitation and cognitive interviewing. Ensure new COA instruments are patient-centered, scientifically robust, and fit-for-purpose for clinical and regulatory use. Internal SME Oversight & Quality Assurance  Serve as subject matter expert overseeing internal project teams executing COA strategy and development work. Review and approve key scientific deliverables to ensure quality, rigor, and alignment with best practices. Mentor and coach COA consultants, supporting capability development across the organization.Business Development & Practice Growth Support business development through proposal leadership, solution design, and client presentations. Contribute to the evolution of COA strategy methodologies, frameworks, and reusable assets.External Scientific Leadership & Visibility  Maintain a strong external profile through publications, conference presentations, and scientific collaborations. Represent IQVIA as a recognized expert in COA science and endpoint strategy. Contribute to academic teaching, advisory boards, or industry working groups where appropriate. Essential experience, skills and education required Deep expertise across COA types (PRO, ObsRO, ClinRO, PerfO) and their application in clinical research. Extensive experience developing COA endpoint strategies across multiple therapeutic areas. Hands-on experience developing new COA instruments, including item writing and qualitative validation. Experience supporting FDA-facing endpoint strategy and regulatory interactions. Ability to mentor junior team members. Excellent scientific writing, presentation, and stakeholder engagement skills. Advanced degree (PhD, MD, PharmD, DrPH, MSc) in a relevant scientific discipline strongly preferred. Strong publication record and recognized credibility in outcomes research or COA measurement science. Well-developed written and verbal communication skills including presentations, chairing meetings, external conference presentations, workshop facilitation, business and report writing.An entrepreneurial nature and interest in developing new client offerings and solutions and in building the capability to deliver the same.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™ – The Human Data Science Company™ – ist ein führender, globaler Anbieter von zukunftsweisender Analytik, Technologielösungen und klinischer Auftragsforschung. IQVIA unterstützt Life Science Unternehmen, Verbände, Institutionen, Kostenträger und weitere Akteure im Gesundheitswesen darin, bessere Ergebnisse in der Gesundheitsversorgung zu erzielen. Werden Sie Teil unserer Community von rund 88.000 Mitarbeiterinnen und Mitarbeitern in über 100 Ländern, die sich dafür einsetzen, das Potenzial von Human Data Science Wirklichkeit werden zu lassen! Ganz gleich, in welche Rolle Sie bei IQVIA einsteigen, es erwartet Sie ein offenes, innovationsfreudiges Umfeld, in dem Sie sich viel bewegen können. Finden Sie heraus, wie Sie Ihre Talente und Ihre Leidenschaften bei IQVIA einbringen können. Im Bereich Commercial Engagement Services (CES) arbeiten wir eng mit unseren Life Sciences-Kunden zusammen und unterstützen sie mit flexiblen Vertriebs- und Personallösungen für nachhaltigen Erfolg am Markt. Dazu gehören integrierte Projektansätze entlang unseres IQVIA-Lösungsportfolios, die wir individuell an Kundenbedürfnisse anpassen und aus einer Hand anbieten. Für einen bundesweiten Teamaufbau im Bereich Gynäkologie suchen wir zum 01.09.2026 mehrere Pharmaberater (m/w/d). Im Gebiet: Großraum Frankfurt Rollenbeschreibung Verantwortung für definierte gynäkologische Zielkunden und Aufbau nachhaltiger KundenbeziehungenUmsetzung des Markteintritts im Bereich Women’s Health auf GebietsebenePositionierung des Produkts sowie Durchführung fundierter FachgesprächeAufbereitung und Präsentation klinischer StudiendatenEntwicklung und Umsetzung individueller Account-PläneSteuerung der Gebietsperformance unter Nutzung von CRM-Tools (z. B. Veeva)Enge Zusammenarbeit mit internen Schnittstellen unter Einhaltung von Compliance-Vorgaben​Erforderliche Qualifikationen Ein abgeschlossenes Studium in Naturwissenschaften oder eine vergleichbare Qualifikation nach §75 AMGGültiger Führerschein sowie Reisebereitschaft innerhalb des jeweiligen GebietsErfahrung oder Kontakte im Bereich Gynäkologie / Women’s Health bevorzugtSicherer Umgang mit Compliance-Vorgaben (inkl. SAMs)Ausgeprägte Kundenorientierung und überzeugendes AuftretenSensibilität und Offenheit im Umgang mit Women’s Health ThemenErfahrung mit CRM-Systemen (z. B. Veeva) von VorteilGute Englischkenntnisse von VorteilDas erwartet Dich bei uns: Ein attraktives Gehaltspaket plus Kundenprämien, vielfältige Corporate Benefits, betriebliche Altersvorsorge sowie 24/7 Unfallversicherung (auch für den privaten Bereich) und exklusive private KrankenzusatzversicherungenEin top ausgestatteter Firmenwagen mit uneingeschränkter Privatnutzung (ohne Zuzahlung) und mit Wahlmöglichkeit des ModellsEine moderne IT-Ausstattung für Deinen modernen digitalen ArbeitsplatzUnser unbefristetes IQVIA Arbeitsverhältnis bietet Sicherheit und eine langfristige PerspektiveWir bieten u.a. tarifliche Sonderurlaubstage, Umzugszuschuss bei betrieblich bedingtem Wechsel deines WohnortsVielfältige und individuelle Weiterentwicklungsmöglichkeiten auch innerhalb von IQVIA (z.B. Führung, Key Account Management, Projektmanagement und vieles mehr)Wir begleiten Dich während Deiner Bewerbungsphase durch individuelle Betreuung/Vorbereitung bis zur Einstellung und auch darüber hinaus während des BeschäftigungsverhältnissesUnser Kunden-Netzwerk reicht vom Start-up Unternehmen bis zum Global Player. Gemeinsam mit Dir finden wir den richtigen Job für Dich! Starte Deine Karriere mit IQVIA! Dein besonders schneller Draht zu uns: Kandidaten-Hotline: 0621-84508113 oder sende uns gerne direkt Deine Bewerbung per Mail an: [email protected] #LI-CES #LI-DNP #LI-SS2 #PharmaceuticalSales #PharmaRepresentative #Pharmacy #FieldSales #Gynäkologie#Woman’s Health 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™ – The Human Data Science Company™ – ist ein führender, globaler Anbieter von zukunftsweisender Analytik, Technologielösungen und klinischer Auftragsforschung. IQVIA unterstützt Life Science Unternehmen, Verbände, Institutionen, Kostenträger und weitere Akteure im Gesundheitswesen darin, bessere Ergebnisse in der Gesundheits-versorgung zu erzielen. Werde Teil unserer Community von rund 90.000 Mitarbeiterinnen und Mitarbeitern in über 100 Ländern, die sich dafür einsetzen, das Potenzial von Human Data Science Wirklichkeit werden zu lassen! Ganz gleich, in welcher Rolle Du bei IQVIA einsteigst, es erwartet Dich ein offenes, innovationsfreudiges Umfeld, indem Du viel bewegen kannst. Finde heraus, wie Du Deine Talente und Deine Leidenschaften bei IQVIA einbringen kannst. Aktuelle, umfassende Marktinformationen und Daten, die wir weltweit gemeinsam mit Partnern im Gesundheitsmarkt erheben, sind ein zentraler Erfolgsfaktor für IQVIA. Neben Pharmagroßhändlern, Krankenhäusern und Ärzten spielen Apotheken eine entscheidende Rolle als Datenpartner. Eine vertrauensvolle und langfristige Zusammenarbeit mit unseren Apothekenpartnern bildet dabei die Basis unseres Erfolgs. Zur Verstärkung unseres Teams suchen wir einen Panel Manager (m/w/d), der Interesse an der Pharma‑ und Healthcare‑Industrie hat und sich schrittweise in ein vielseitiges Aufgabenfeld im Apothekenumfeld entwickeln möchte. Deine Aufgaben: Du unterstützt das Team bei der Betreuung eines großen Apothekenpanels und im Zusammenspiel mit Apotheken-Softwarehäusern/-Rechenzentren und arbeitest eng mit erfahrenen Kolleg:innen zusammen. Gemeinsam mit dem Team bist Du Ansprechpartner:in für unsere Apothekenpartner bei Fragen rund um Verträge, Abrechnungen und die Zusammenarbeit. Du wirkst bei der Sicherstellung und Weiterentwicklung von Prozessen zur Daten‑ und Qualitätskontrolle mit. Du unterstützt bei der Einführung neuer Dienstleistungen und Projekte und lernst dabei, verschiedene interne und externe Stakeholder zu koordinieren. Du stehst im regelmäßigen Austausch mit Apothekenpartnern – telefonisch, digital und perspektivisch auch vor Ort. Du arbeitest Dich in pharmazeutische Datenbanken ein und unterstützt projektbezogen bei inhaltlichen Fragestellungen zum deutschen Arzneimittelmarkt. Du informierst Dich aktiv über Neuerungen im Apotheken‑ und Pharmamarkt und bringst eigene Ideen ein. Dein Profil:  Abgeschlossenes Studium der Pharmazie oder ein vergleichbares Studium mit Bezug zum Gesundheitswesen. Erste praktische Erfahrungen in einer Apotheke oder in einem apothekennahen Umfeld sind wünschenswert. Interesse an Kundenkontakt und Service‑orientierter Arbeit. Freude daran, Dich in neue IT‑Anwendungen einzuarbeiten und diese sicher anzuwenden. Analytisches Denkvermögen und Interesse am Umgang mit Zahlen und Daten. Sehr gute Kommunikationsfähigkeit in Deutsch sowie gute Englischkenntnisse. Teamgeist, Lernbereitschaft und der Wunsch, Dich fachlich und persönlich weiterzuentwickeln. Was Dich erwartet: Ein strukturierter Einstieg in die Pharma‑ und Healthcare‑Industrie. Mitarbeit in einem kollegialen, erfahrenen Team mit klarer Unterstützung und Einarbeitung. Spannende Einblicke in das Apothekenumfeld, Marktanalysen und datenbasierte Entscheidungsprozesse. Entwicklungsmöglichkeiten in einem internationalen Unternehmen mit hoher Marktrelevanz. Wir freuen uns auf Deine vollständige Bewerbung mit Angabe des frühestmöglichen Eintrittstermins und Deiner Gehaltsvorstellung – bitte vorzugsweise online 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.

Join IQVIA as a SrCRA II/III (m/w/d) in our Clinical Site Management department home-based throughout Germany. You will focus on a comprehensive clinical trial management in a variety of indications and learn about the diverse scientific approach of the sponsors. Beside establishing strong relationships with the global study team and the involved investigators, you will conduct monitoring on complex clinical trials for different pharma companies and assure their adherence to good clinical practices and study protocols. With strategic site relationship managers supporting you throughout your role, this is a fantastic opportunity for you to embed yourself in the wider clinical operations team and work on ground-breaking new medicine development. Your responsibilities will include: Performing site selection, initiation, monitoring and close-out visits. Supporting the development of a subject recruitment plan. Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution. Collaborating with experts on study sites and client representatives. Qualifications: University Degree in life science or other scientific discipline or apprenticeship in health care. Minimum of six years of on-site monitoring experience Knowledge of applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Strong written and verbal communication skills, attention to detail and ability to work in a fast pace environment. Good command of German and English. Flexibility to business travel up to 60% of working time. Driver’s license class B. What you can expect: Resources that promote your career growth. Leaders that support flexible work schedules. Programs to help you build your therapeutic knowledge. Dynamic work environments that expose you to new experiences. Home-office, company car/car allowance, accident insurance, pension and more. Whatever your career goals, we are here to ensure you get there! Please apply with your English CV and motivation letter. 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.

JOB OVERVIEWPerforms 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 ABILITIESExperience working in Drug Discovery, clinical trial conduct, clinical data management or related industries.Excellent critical thinking and analytical skills, strong attention to detailEffective written, interpersonal, and verbal communication skillsStrong influencing, problem resolution, motivation, and negotiation skillsSolution-oriented approach to challengesSound leadership and customer service skillsCompetent presentation skills meeting the needs of all levelsAbility to establish and maintain effective working relationships with team members, management, operations staff, clients, and executive managementAbility to lead effective meetingsStrong organizational and time management skillsAbility to manage multiple dependencies across multiple systems to reach a final deliverableAbility to establish and maintain effective working relationships with teams involved in study start upMINIMUM EXPERIENCEBachelor 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.

Job OverviewIQVIA is hiring to expand our dedicated Real World Evidence (RWE) FSP team, working fully within the environment of a prominent Pharma company. Associate Clinical Project Managers (aCPM) are an integral part of clinical trial delivery, liaising with clinical teams to improve patients’ lives by bringing new drugs to the market faster. The aCPM is a member of the core project team responsible for project delivery of clinical and RWE studies across three therapeutic areas (oncology, virology, inflammation) to meet contractual requirements in accordance with SOPs, policies and practices. The aCPM supports the efforts of the Operations Lead and Project Managers to drive operational excellence and strategic leadership with our customers.Essential Functions• Provide input into the development of integrated study management plans with the core project team and/or sub-team.• Accountable for assigned portion of clinical studies while optimizing speed, quality and cost of delivery and ensuring consistent use of study tools and training materials and compliance with client standard processes, policies and procedures.• Collaborate with other functional groups where necessary to support milestone achievement and to manage study issues and obstacles.• Monitor progress and prepare/present project and/or sub-team information proactively to internal stakeholders. Support the project leader to prepare/present project and/or sub-team information proactively to external stakeholders.• Identify risk (positive and negative) and contingencies and partner with project leader in problem solving and resolution efforts.• Achieve project quality by identifying quality risks and issues, responding to issues raised by project sub-team members and partner with project leader planning/implementing appropriate corrective and preventative action plans.• May serve as primary (for small projects) or back-up project contact with customer.• Lead the efforts of a project sub-team, responsible for managing cross-collaboration of the sub-team to support milestone achievement and to manage issues and obstacles.• Support the project leader in ensuring the financial success of the project.• Forecast and identify opportunities to accelerate activities, build best practices, and transition knowledge from clinical to RWE pipeline• Identify changes in scope and partner with project leader to manage change control process as necessary.• Identify lessons learned and implement best practices.• May be assigned as the primary contact for vendors leading project vendor management and vendor management related activities as per project requirementsQualifications• Associate's Degree In life sciences or related field required Req Or• Bachelor's Degree In life sciences or related field required Req• 2 years clinical research experience Req• Requires intermediate level knowledge of principles, theories, and concepts of a job area, typically obtained through advanced education combined with experience.; Req• Knowledge of clinical trials - Knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements i.e. ICH GCP and relevant local laws, regulations and guidelines, towards clinical trial conduct. Broad protocol knowledge, therapeutic knowledge desired.;• Communication - Strong written and verbal communication skills including good command of English language. Strong presentation skills.• Problem solving - Strong problem solving skills.• Organisation - Planning, time management and prioritization skills. Ability to organize resources needed to accomplish tasks, set objectives and provide clear direction to others, experience planning activities in advance and taking account of possible changing circumstances.• Prioritisation - Ability to handle conflicting priorities.• Quality - Attention to detail and accuracy in work. Results-oriented approach to work towards delivery and output.• Collaboration - Ability to establish and maintain effective working relationships with coworkers, managers and clients. Strong customer service skills.• Cross-collaboration - Ability to work across geographies displaying high awareness and understanding of cultural differences. 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 $68,400.00 - $171,000.00. 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.

Job Overview: Review, assess and process Safety data and information, across service lines, received from various sources and distribute reports/data onwards to both internal and external third parties following applicable regulations SOPs and internal guidelines under guidance and support of senior operation team members.Essential Functions: To Prioritize and complete the assigned trainings on time. Process Safety data according to applicable regulations, guidelines, Standard Operating procedures (SOPs) and project requirements.To perform Pharmacovigilance activities per project requirement including but not limited to, collecting and tracking incoming Adverse Events(AE)/endpoint information determining initial/update status of incoming events database entry coding AE and Products, writing narratives, Literature related activities as per internal/ project timelines.Creating, maintaining and tracking cases as applicable to the project plan.Identify quality problems, if any, and bring them to the attention of a senior team member.To mentor new teams members, if assigned by the Manager.Attend project team meetings and provide feedback to operations manager on any challenges/issues or successes.Qualifications: High School Diploma or equivalent Scientific or healthcare discipline or allied life sciences background with 1-1.5 years of relevant experience. Good knowledge of medical terminology.Working knowledge of applicable Safety Database (ARGUS).Good working knowledge of Microsoft Office and web-based applications. Ability to multi-task, manage competing priorities and deadlines.Willingness and aptitude to learn new skills across Safety service lines. Ability to work as a Team Player, contribute and work towards achieving Team goals. Ensure quality of deliverables according to the agreed terms. Use of telephone and face-to-face communication requiring accurate perception of speech. May require occasional travel. May require on-site work (in a hybrid capacity, 1 day a week)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 $44,900.00 - $112,100.00. 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.

To be eligible for this position, you must reside in the same country where the job is located. VP, Business Development Job OverviewLeadership role for a sales team responsible for key accounts in North America reporting to the SVP. Responsible for developing long-range strategic plans, coaching and developing team members, achieving sales targets with an emphasis on creating and sustaining business growth. Direct business development activities to achieve sales and new business goals from identification through contract award. Establish and maintain relationships with senior levels within customer organization, and within IQVIA.Essential Functions Manage staff in accordance with organization’s policies and applicable legislation. Responsibilities include sales development and coaching of team members, planning, assigning, and directing work; appraising performance and guiding professional development; rewarding and disciplining employees; addressing employee relations issues and resolving problems. Provide leadership and direction to business unit in its efforts to increase presence and market share in applicable markets. Collaborate with internal departments in identifying/implementing business development opportunities to expand the services and continually improve the business performance of FSP and full-service clinical development phase I-IV services. Provide direction and serve as a resource for sales team members, including; performance management, career progression, and professional development. Aid sales team in the Identification and alignment of capabilities with current and potential customer requirements. Lead/Participate in Governance Committee with customers. Research and identify target markets, build relationships, perform and deliver in-depth presentations, strategic analysis, and execution of implemented plans. Continuously develop and cultivate business relationships within senior levels of customer organizations. Provide senior level representation for the Company’s interaction with perspective customers, development teams, and external consultants. Actively participates in proposal and strategy development, preparation meetings and bid defense meetings. Represent respective Sales Team to Senior Management on key business updates related to sales activities. Ensure that the sales team members are sufficiently trained to meet their job objectives. Qualifications Bachelor's Degree, Masters Preferred 17+ years of progressively more responsible experience in CRO services or large pharmaceutical or life science companies including 10 years management experience Req Or Equivalent combination of education, training and experience Req Unquestionable personal and professional integrity Solid understanding of commercialization and the principles of drug discovery and development Strategic business and Industry awareness and the ability to translate emerging Industry trends relevant to the organization Excellent Analytical skills and experience in evaluating and managing business plans Proven experience conducting and negotiating deals Excellent Attention to detail and ability to work simultaneously on multiple priorities Adaptability and flexibility to changing priorities Excellent presentation, communication, and negotiation skills Proven previous management experience and success Experience and ability to progressively coach and mentor individuals Proven ability to empower and develop people and help them achieve goal Ability to establish and maintain effective working relationships with coworkers, managers and clients 40%+ travel is required (based on location) 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 $155,800.00 - $434,200.00. 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.

At IQVIA Biotech, we are redefining what’s possible in clinical development—and our VP, Immuno-Oncology and Cell and Gene Therapy (CAGT) role is at the forefront of that transformation. This is a highly dynamic, strategic leadership position designed for a visionary expert who thrives at the intersection of science, innovation, and operational execution. As Vice President, you will play a pivotal role in shaping and growing our Immuno-Oncology and CAGT portfolio, partnering with biotech innovators to bring breakthrough therapies to patients faster. You will lead cross-functional teams, influence high-impact decisions across complex clinical programs, drive operations across a rapidly growing book of work, and serve as a trusted advisor to both internal stakeholders and external clients. We are seeking a leader with a deep grounding in both CRO and biotech environments—someone who understands the agility and urgency of biotech, combined with the operational rigor and scalability of a CRO. Your experience allows you to anticipate client needs, navigate evolving scientific landscapes, and deliver tailored, high-quality solutions in a fast-paced, ever-changing setting. What makes this role exciting: Dynamic scope: No two days are the same—you’ll engage across strategy, operations, client engagement, and scientific leadership.Industry impact: Work directly on cutting-edge immuno-oncology and CAGT therapies that are reshaping cancer treatment.Collaborative influence: Partner with world-class scientists, clinicians, and biotech leaders globally.Growth mindset: Help expand IQVIA Biotech’s Immuno-Oncology and CAGT capabilities and footprint as the market evolves.This role is ideally suited for someone who is entrepreneurial, adaptable, and deeply passionate about advancing oncology innovation, with the credibility and experience to lead operations in both CRO and biotech settings. If you are energized by complexity, driven by purpose, and ready to make a meaningful impact in Immuno-Oncology and CAGT space, this is your opportunity to lead at scale. Qualifications• Bachelor's Degree Life sciences or related field required• Requires an experienced clinical operations leader, with greater than 15 years clinical research experience in GCP and drug development including 10 years of leadership experience including multi-regional and global focus or equivalent combination of education, training and experience.• Experience and knowledge obtained through advanced education, combined with operational and strategic experience. Demonstrable people leadership skills coupled with the ability to motivate teams and lead by example. Leading in a complex environment, whilst being flexible and agile to changing needs are critical success factors.• Requires advanced business knowledge, general management and leadership capability to lead business or functional teams.• Business Acumen - High degree of business acumen, coupled with the ability to drive productivity and achieve financial goals, whilst quality & delivery is maintained. Drive innovation, process improvement and adoption of innovative technologies as part of Core. Balance operational and strategic priorities, with an ability to think/act strategically, establishing a vision, execution and adjustment.• Financial management - Knowledge of clinical research financial parameters and project financial tracking and accounting methods.• Therapeutic expertise - In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines In depth technical and/or therapeutic expertise and knowledge of study, project and drug development processes.• Communication skills - Excellent communication and interpersonal skills, including strong command of English language. Strong presentation skills.• People leadership - Highly effective team leadership skills. Strong influencing and negotiation skills.• Customer Management - Excellent customer service skills: active listening, assertive communication, ability to compromise, influence and achieve win-win outcomes.• Collaboration - Sound judgment and decision-making skills. Ability to establish and maintain effective working relationships with coworkers, managers and clients. Proven ability to work through others in a global matrix environment to deliver results to the appropriate quality and timeline metrics.• IT literate - Strong software and computer skills, including MS Office applications. 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 $173,600.00 - $483,600.00. 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 Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile, therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to patients faster. Drive global clinical trials from first site activation to final patient visit—own the strategy, accelerate delivery, and shape the future of clinical research worldwide. Required Experience✅ 2+ years of global study management experience✅ Experience across multiple countries/regions✅ Phase I–III clinical trials experience (Phase III required)✅ Oncology experience required✅ Ability to work across multiple therapeutic areasJob OverviewWe are seeking a Global Study Manager responsible for the end-to-end planning, execution, and delivery of clinical trial site management activities across global studies. This role ensures successful site selection, activation, monitoring oversight, and closeout—while balancing speed, quality, and cost. You will serve as the primary point of contact for clients, lead cross-functional teams, and ensure compliance with ICH-GCP, regulatory requirements, and study protocols. This is a highly visible role that combines strategic leadership, operational execution, and financial oversight. Key ResponsibilitiesGlobal Study & Site LeadershipLead site management strategy from study award through close-outOversee site identification, selection, activation, and recruitment performanceEnsure clinical monitoring processes meet study needs and timelinesPartner with CRAs to optimize enrollment, data quality, and complianceProject & Stakeholder ManagementServe as primary client contact and own key customer relationshipsLead cross-functional teams across regions and culturesFacilitate internal and external meetings, including executive presentationsDrive collaboration across stakeholders, vendors, and functional leadsOperational Excellence & Risk ManagementDevelop and manage integrated study plans and risk mitigation strategiesProactively identify risks and implement corrective/preventative actionsMonitor study timelines, enrollment trends, and data quality metricsEnsure compliance with GCP, SOPs, protocols, and regulatory standardsFinancial & Contract ManagementManage study financials, including forecasting and revenue accelerationIdentify and manage out-of-scope work and change ordersOversee Billing Unit Reviews (BURs) and expense approvalsTrack performance against budget and Estimate at Completion (EAC)Quality & ComplianceMaintain TMF health and ensure timely document submissionDevelop quality monitoring plans and compliance metricsEnsure adherence to study tools, training materials, and processesTeam Leadership & DevelopmentLead and mentor cross-functional project teamsSupport CRA and team training on therapeutic areas and study-specific needsFoster collaboration, knowledge sharing, and continuous improvementQualificationsRequiredBachelor’s degree in life sciences or related field5+ years of clinical research/monitoring experience, including 2 years in a clinical study management roleStrong knowledge of ICH-GCP, FDA regulations, and clinical trial processesExperience managing global clinical trials and multi-regional teamsDemonstrated experience in project financial managementCore CompetenciesExceptional communication and stakeholder management skillsStrong problem-solving and risk mitigation capabilitiesAbility to influence without authority in matrix organizationsHigh attention to detail and quality-driven mindsetProficiency in Microsoft Office and clinical systems (e.g., CTMS, EDC)Why Join UsWork on cutting-edge global trials across therapeutic areasCollaborate with top talent in a dynamic, global environmentMake a direct impact on patient outcomes worldwideIQVIA 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 $93,100.00 - $232,800.00. 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.

Responsibilities Delivers profitability and recognition for the organization by selling and providing services to customers utilizing organization tools, techniques, and intellectual capital to assist the healthcare industry by bettering processes, implementing new technologies; and accruing new technical capabilities to meet pharmaceutical and medical demands.Maximizes sales growth by relying on a comprehensive knowledge of one or more therapeutic disciplines and/or specialty areas to secure repeat business and gain customer loyalty.Targets, promotes, and sells specialized products or services; identifies target customers and producers; achieves sales targets; maintains an up-to-date understanding of products and clinical efficacy, proximity to specialist market trends or developments and customer satisfaction.In line with Company strategy and objectives, maximize sales growth within in a specified geographical territory or target industry, relying on developing knowledge of one or more therapeutic disciplines and or specialty areas in order to secure repeat business and gain customer loyalty. This is generally achieved by educating and informing the target audience on the features and benefits of the specialty product(s) versus competitor products in order to increase prescriptions and or use by the healthcare professionals.Achieve assigned activity goals and targets for the territory as agreed with the reporting manager.Within a specific geographical territory, identify target customers and physician profiling while maintaining and analyzing customer records.Conduct sales interviews, carry out pre-call planning and preparation and develop a self analytical approach in order to identify learning areas from each call.Demonstrate a good understanding of the product (s) clinical efficacy and be able to state the features and benefits of the customer’s products based on a developing understanding of the specialty area or therapeutic discipline.Successfully manage objections and or issues raised, escalating more sensitive or complex queries.Maintain records in the reporting systems within the required timescales.Effectively utilize the relevant software (e.g. Electronic Territory Management System, CRM systems) to maintain records updated and to report daily callsCoordinate group events related to speciality area to optimize business while complying with relevant country legislation.Keep Line Manager informed about changes in competitor activities and other market changes.Attend training courses and or seminars to continue to develop and deepen knowledge within specialty and disease areas and read relevant publications as per customer profile.Keep all Company equipment safe and in a good state of repair.Share experiences, ideas and techniques in order to assist with the sales training of colleagues.Discuss, agree and document assigned activity, Key Performance Indicator tools, and targets as agreed with Line Manager.Successfully complete career development courses and additional training as required by the customer.Ensure the reporting of any identified Adverse Events in line with prevailing process and guidelines.Project a professional impression of the Company and act in accordance with the relevant Pharmaceutical Industry’s Code of PracticePerform other duties as assigned.Requirements Require 1 - 2 years of prior relevant experience in Medical Sales .Bachelor's Degree in Life Sciences / Pharmacy / Business or related fieldGood understanding of Healthcare Market and related procedures.   Fluency software operating systems, such as MS Office and customer relationship management systems.   Effective verbal and written communication skills.   Ability to conduct face to face presentations to customers. Ability to establish and maintain effective working relationships with coworkers, managers and clients#LI-CES#LI-PK1#LI-DNP 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.

Rol  Buscamos un Líder de Transformación Digital para nuestra unidad de negocio de Panel. Este rol tendrá como misión principal impulsar la migración de procesos manuales hacia soluciones automatizadas, logrando una operación más eficiente, escalable y orientada al cliente.   Este rol será un habilitador clave para optimizar procesos, reducir complejidad operativa y liberar capacidad del equipo, permitiendo mayor foco en actividades de valor para el negocio y el cliente.  Tareas  Entendimiento de los pipeline de información internos  Mapeo de procesos con stakeholders internos y externos  Automatizar procesos clave (reporting, data y workflows)  Estandarizar entregables para clientes externos  Reducir tiempos y errores operativos - generando alertas en los procesos de ingesta de datos y procesamiento  Mejorar los modelos de datos existentes  Reorientar el esfuerzo del equipo hacia actividades de mayor valor (Client Success)  Análisis con stakeholders externos para diseñar soluciones que generen valor a clientes externos  Competencias clave  Pensamiento analítico y estructurado  Foco en eficiencia y mejora continua  Capacidad de automatización y estandarización de visualizadores  Atención al detalle  Proactividad y orientación a resultados  Trabajo colaborativo entre stakeholders    Herramientas  SQL   Herramientas de visualización (Power BI / Tableau) DAX  Excel avanzado (tablas dinámicas, Power Query)  Python (automatización / data processing)  Herramientas de automatización (Power Automate o similares)  ETLs    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 provides scientific services spanning clinical trials, real world evidence, and consulting in all areas of the product lifecycle. The Patient Centered Solutions (PCS) team leads the industry in generating data to ensure that the patient voice is incorporated into the development and commercialization of medication and other drug/non-drug interventions. We focus on understanding and meeting the needs of our clients – mostly life science/pharmaceutical companies – through the application of broad consulting expertise and technical scientific knowledge to design scientifically rigorous research. This research is broad and includes qualitative (e.g. interviews, focus groups), quantitative (e.g. clinical outcome assessments (COAs)/patient-reported outcomes (PROS), preference research) and passive (e.g. digital health technology tools) approaches to understand patient, caregiver and healthcare professional experiences and expectations of disease and treatment.To meet our client expectations and retain the excellent reputation built up over time the IQVIA PCS team is committed to recruiting, training and supporting driven individuals who have both consulting skills and life science skills that can be applied to PCS research activities. Individuals joining us are assured of a rewarding and progressive career in patient-focused research. You’ll have the opportunity to address challenging client issues, across multiple geographies with a hands-on influence in developing and delivering solutions.  We operate in a truly multi-cultural, collegial and collaborative work environment that is rich in development and growth. Role & Responsibilities The role-holder will need to be a committed individual, who combines high emotional intelligence and excellent communication skills. They will thrive in a fast-paced environment and be comfortable managing conflicting priorities. The environment is dynamic and ever-changing, moving at the pace of our clients’ needs and the candidate will be expected to understand the sense of urgency that is synonymous with the business. As a Consultant, ClinRO Services within the PCS team at IQVIA, you will directly administer assessments to participants in a clinical trial, or evaluate the quality of assessments performed by others and provide feedback regarding interview technique and scoring. Responsibilities include: Review of scales administered by raters in a clinical trial to ensure that assessments are being conducted in a standardized manner to ensure data reliability. Evaluation the quality of assessments, conducting live interactions with raters to discuss assessment methodology, scoring technique, and to provide guidance, as necessary. Evaluate case data and appropriately prepare for discussions with raters (e.g., prepared to discuss relevant issues and scale items, and have necessary documents available). Complete rater interactions and assigned tasks as scheduled. Responsible for timely submission of all documentation associated with assigned tasks. Participate in all orientation, training and calibration activities as required. Functional assessments of rater performance (e.g., mock interview) and assistance in preparing and disseminating communications. Contacting clinical trial participants remotely (e.g., via proprietary app, Engage) to administer assessments, and will appropriately document resultant information (e.g., notes, scores) What do you need to apply? Minimum of a Master’s degree (MA/MS) in Psychology, Counseling, Psychiatric, Nursing or Social Work, or equivalent. Minimum of 3 years’ clinical experience working with schizophrenia and major depressive disorder populations. Minimum of 3 years clinical experience working administering psychiatric assessments including the PANSS, to these populations is also required. Clinical Trials experience preferred. Advanced level of English. Home based position in Latin America. 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.

Job Purpose The Associate Director Senior Study Lead is the leader of the cross-functional clinical trial team (CTT), who guides planning and management of the assigned clinical study/studies end-to-end to achieve objectives. Accountable for proactive, iterative operational planning with effective contingencies and embedded risk management mindset in CTT. Oversees budget and people allocation within assigned study/studies. Contributes in promoting operational excellence through process improvement and knowledge sharing across studies. Fosters an empowered, psychologically safe organization that can navigate a matrix environment, learns, and adjusts quickly to changing conditions and business needs. Key accountabilities Executes and delivers clinical studies; guides planning and decision making at study-level Acts as the CTT product owner with clear and focused duties and responsibilities per the agile ways of working Active member of a Clinical Operations community within the study leadership organization Promotes operational excellence in the shared development of global clinical study protocol(s), clinical study report(s), and other study-related documents Deliverables Patient recruitment, clinical data, study documentation and study reports Efficient delivery of the protocol, ICF, Monitoring Plan, and CSR in quality and on time Cost effective management of study budget Proactive, iterative operational planning with effective contingencies and embedded risk management mindset in CTT Key expertise and skillset Bachelor's degree in life sciences/healthcare (or clinically relevant degree) is required. Advanced degree is strongly preferred. ≥ 4 years of recent involvement in clinical research or drug development in an academic or industry environment spanning clinical activities in Phases I through IV of standard to high complexity and priority. ≥ 3 years of recent contribution to and accomplishment in all aspects of conducting clinical studies of standard to high complexity and priority (e.g., planning, executing, reporting and publishing) in a global/matrix environment in pharmaceutical industry or a contract research organization, including expert knowledge of international standards (GCP/ICH), health authorities (FDA/EMA), local/National Health Authorities Experience in managing people globally in a complex matrix environment preferred Management of virtual teams. Proven ability and strong experience leading teams and building capabilities Experience in developing effective working relationships with internal and external stakeholders Excellent communicator and presenter (oral and written); ability to communicate at all levels Excellent organization and prioritization Strong negotiation and conflict resolution skills and enterprise mindset, demonstrated by ability to drive for aligned solutions Fluent English, oral and written Location: Home-based Please note this role is not eligible for the UK visa sponsorship. Please note: due to sponsor requirements for the role only candidates based in the listed location/s will be considered. Any applications from candidates based outside of these locations will not be considered. 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 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 Data Manager opportunities across multiple teams - allowing us to match you with the best-fit project and client environment for your experience and interests!  IQVIA is seeking experienced Clinical Data Management Leads to oversee end-to-end data management delivery for global clinical trials. You’ll ensure quality, accuracy, and compliance while leading cross-functional teams that help bring new therapies to life. This is a remote/WFH position with all necessary equipment provided.What You’ll Do Lead data management for complex, global clinical trials from study setup to database lock.Serve as the main client contact for all data management deliverables.Oversee SAE, PK, and external data reconciliation and database deployment.Manage timelines, budgets, and resource allocation to meet customer expectations.Mentor junior data management staff and promote best practices.Drive process improvements and ensure regulatory and SOP compliance.Who We’re Looking For Ideal candidates will have.... Bachelor’s degree in life sciences, health, clinical, biological, or mathematical field.No less than 10 years of direct clinical data management experience, with 5+ years in a Lead Clinical Data Management role.Your previous roles/job titles may include Clinical Data Manager, Senior Clinical Data Manager, Lead Data Manager, Principal Data Manager, and/or Data Management Project Manager.Proven success managing large global studies (1000+ patients).Expertise with Medidata Rave, Oracle InForm, or similar EDC systems.Strong understanding of GCP, ICH, and clinical research processes.Excellent communication and leadership skills.What IQVIA Offers Fully remote role – company equipment providedCompetitive salary and performance-based incentivesCareer growth and learning opportunities through mentoring and internal mobilityInclusive, global culture focused on innovation and collaborationWhat to Expect After Applying Recruiter video chat (20 min)Hiring manager interview (1 hour, MS Teams - Offer decisions are typically made within one or two weeks of the final interview.)  Apply now to join IQVIA, where your expertise shapes the future of data-driven healthcare! 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. The potential base pay range for this role, when annualized, is €30,800.00 - €62,400.00. 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.

To be eligible for this position, you must reside in the same country where the job is located. Role will be required to travel. We are seeking an inspirational leader to shape and elevate our Global enterprise Advisory Services presence across the United States, Japan, and Asia/Pacific. In an increasingly complex market, our HQ, regional HQ, and enterprise clients face deep challenges. The Global Advisory Leader will drive the strategy of the Global Advisory organization as trusted partners to these clients, developing deep understanding of their challenges and consistently earning IQVIA the opportunity to support them. As the senior leader of DTAS’ Global Advisory Services, you will shape commercial strategy, drive growth, and ensure exceptional delivery across a global and cross-functional team. You will drive strategies and synergies across the regional Advisory teams, act as a trusted advisor to senior stakeholders, deepen client intimacy, and champion integrated solutions across a range of asset and above-asset priorities. You will bring executive presence, demonstrating the strategic influence, commercial acumen, and people leadership central to the success of the organization. What You’ll Do: Be the senior face of IQVIA’s Global Advisory Services, trusted by executive‑level and other senior stakeholders as a strategic advisor, sounding board, and thought‑partnerSet and own the Advisory Services growth agenda — partnering closely with the regional Advisory leaders who are responsible for defining key client priorities, shaping large‑scale opportunities, and driving year‑over‑year expansion and customer satisfactionModel deep client intimacy and exemplify best‑in‑class client leadership, operating close to your customers, regularly present onsite, and deeply embedded in their strategic prioritiesDrive the integration of AI and new technologies into Advisory Services offerings and commercial strategy, positioning AI-enabled advisory as a core growth driver.” and “Continuously assess emerging AI/ new technologies and innovation trends to shape Advisory Services strategy and anticipate client needs.Facilitate cross‑functional collaboration to leverage expertise both within Advisory Services (brand strategy, portfolio strategy, value & access, digital health) and within the broader DTAS portfolio (data strategy, architecture, outsourcing, technology) — fostering a culture of excellence, collaboration, and innovation.Ensure high-impact delivery, holding regional clusters accountable in ensuring work is insight‑rich, strategic, rigorous, and reflective of the high expectations of our customers; further, you will ensure each reginal cluster works with their peers across Advisory Services to ensure a consistent and high standard of deliverable quality and customer experienceCultivate and nurture top talent, coaching and elevating emerging leaders, providing crisp direction, and creating an environment where teams thrive and grow.Inform and deepen IQVIA’s Thought Leadership and insight, collaborating with IQVIA’s Thought Leadership organization and front-line practitioners to shape, refine, and communicate strategic insights about critical issues facing our clientsInfluence across the enterprise, collaborating closely with other DTAS leaders, GADs, Client Partners, and senior executives to lead and shape client engagement on priority topics and accelerate impactOwn your business, delivering on customer revenue and margin targetsBuild and lead a unified global Advisory Services community, fostering collaboration, capability building, and consistency across regionsWhat You Bring Experience operating at an Executive level in a top-tier consulting environment or comparable internal strategy/advisory leadership.A track record of owning and growing major client relationships, with deep comfort engaging senior decision-makers.Strong commercial acumen: opportunity shaping, complex pursuit leadership, customer value articulation, senior stakeholder orchestration.A leadership style that inspires confidence, unlocks team performance, and elevates the bar for consulting excellence.Ability to lead, inspire, and develop multi-disciplinary teams in a dynamic, evolving environment.Passion for client engagement and a pronounced ability to operate with high presence on client site, building trust through proximity, responsiveness, and insight.Deep intellectual curiosity and learning agility: a pronounced ability to learn and digest new content and to apply it to customer challenges and prioritiesExceptional communication, storytelling, and influence skills — able to simplify, inspire, and drive alignment across diverse groups.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 $183,400.00 - $512,200.00. 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.

Job OverviewIncludes providing education to health care prescribers and their staff on the proper use of designated treatments for assigned disease area or reinforcement of study protocols as related to a clinical trial. Essential Functions• Within a specific geographical territory, identify target customers while maintaining and analyzing customer records.• Accurately complete internal electronic monitoring and reporting systems in accordance with program timescales.• Organize and hold group events to optimize program delivery while complying with relevant country legislation.• Maintain an up to date technical knowledge of specialty and disease areas and relevant publications as per customer profile.• Keep all Company equipment safe and in a good state of repair.• Project a professional impression of the Company and act in accordance with the relevant Pharmaceutical Industry’s Code of Practice.• Comply with local confidentiality requirements.• Understand and adhere to Standard Operating Procedures (SOP's).• Support clinical change through program delivery.• Communicate the aIQVIA and objectives of the program to all relevant health service and local personnel.• Implement the program processes within potential sites such as honorary contracts, management protocol, search criteria, clinical pathway, feedback mechanisms and customer satisfaction reports.• Sort and filter information using excel software to prioritize clinical information according to program objectives.• Mentor less experienced HMS Advisors.• All HMS personnel are required to undertake Adverse Events and Product Complaint (where appropriate) Training, and are responsible for reporting adverse events and product complaints in line with requirements, as applicable.• Perform other duties as assigned. Qualifications• Bachelor's Degree Life Sciences or related field Req Or• High School Diploma or equivalent  Req• 5 years relevant experience or equivalent combination of education, experience and training. Req• Make plans to obtain any industry qualifications essential to job role.• An understanding and working knowledge of the Pharma Market and the local Health Service environment.• Fluency with software operating systems, such as MS Office and customer relationship management systems.• Effective verbal and written communication skills.• Ability to conduct face to face presentations to customers.• Ability to prioritise and coordinate multiple work requirements to meet deadlines.• Ability to establish and maintain effective working relationships with coworkers, managers and clients 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 is 25.00 per hour. 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.

¡Únete a nosotros en nuestro emocionante trayecto! IQVIA ™ es The Human Data Science Company ™, enfocada en el uso de datos y ciencia para ayudar a los clientes de la salud a encontrar mejores soluciones para sus pacientes. Formada a partir de la fusión de IMS Health y Quintiles, IQVIA ofrece una amplia gama de soluciones que aprovechan los avances en información, tecnología, análisis e ingenio humano para impulsar la atención médica. Actualmente nos encontramos en la búsqueda de profesionales de áreas administrativas que quieran ser parte de un gran proyecto con una importante farmacéutica multinacional. ANALISTA DE DATOS Objetivo del cargo La responsabilidad principal es prestar soporte al equipo del proyecto asignado, desarrollar y analizar las bases de datos a través de diferentes herramientas, manejo avanzado de Excel y manejo de Power BI, llevar el control y auditoria de la data de CRM, indicadores, inventarios, etc. Diseño de estrategias a partir de los datos buscando patrones y anomalías dentro de ellos, asegurando la calidad de la información. Principales Funciones Identificar y organizar datosUtilizar herramientas especializadas para extraer los datos necesariosResponder a consultas relacionadas con datos y hacer un seguimiento de estasAnálisis de datos para identificar tendenciasEstablecer procesos y sistemas para que el trabajo con datos sea más eficienteInvestigar nuevas formas de hacer uso de los datosProducir informes y gráficos comunicar tendencias dentro de los datos a no especialistasPresentar información generada a partir de datos a clientes y gerentes.Requisitos Educación: Profesional en Ciencias de la computación o carreras afines.Experiencia: 1 año como Analista de Datos (pueden ser prácticas).Deseable experiencia en Lab. Farmacéutico.Conocimiento y experiencia en data IQVIA (indispensable)Conocimientos en uso de QlikView, Data warehouse, bases de datos estructuradas y lenguaje SQL.Generación y seguimiento de métricas e indicadores de gestión (KPIs).Desarrollo de reportes dinámicos y estáticos.Herramientas informáticas de gestión e inteligencia de negocios (BI).Residencia en Bogotá¡Estamos en búsqueda del mejor talento!#LI-CES 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.

Job OverviewUnder general supervision, perform tasks at a country/region level associated with site activation activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include feasibility or maintenance activities.Essential Functions• Under general supervision, perform feasibility, site activation and some maintenance activities in assigned studies for investigative sites, according to applicable regulations, SOPs and work instructions, working closely with the Site Activation Manager (SAM), Project Management team, and other departments as necessary. Review documents for completeness, consistency and accuracy, under guidance of senior staff.• Prepare site documents, reviewing for completeness and accuracy.• Inform team members of completion of regulatory contractual. and other documents for individual sites.• Distribute completed documents to sites and internal project team members.• Support the updating and maintenance of internal systems, databases, tracking tools, timelines and project plans with accurate and complete project specific information.• Review, track and follow up the progress, the approval and execution of required documents such as questionaires, CDAs, regulatory, ethics, Informed Consent Form (ICF) and Investigator Pack (IP) release documents.Qualifications• Bachelor's Degree Life science or related field Req• With 2 years’ experience in a healthcare environment or equivalent combination of education, training and experience. Established individual contributor who works under general supervision. Delivers objectives that significantly impact results for a job area. Tasks are not typically routine, and may require applying discretion within broad operational boundaries and procedures. Problems faced are general and may require some analysis to resolve. 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.

职责 • 准备和组织各种临床研究方案的研讨活动，并与主要研究者或者该治疗领域的专家进行密切 的沟通有关研究方案的事宜； • 根据公司SOP及客户的要求，负责临床研究项目相关的医学撰写工作，如临床研究方案及临床 研究总结报告等的撰写。 • 负责项目的医学审阅工作，如审阅研究方案、知情同意书、研究者手册、和/或病例报告表、 统计分析计划表（SAP）、临床研究总结报告和不良事件的医学编码。 • 根据公司SOP及项目的要求，制定医学监查计划，确保项目质量和安全性，包括但不限于SAE 和方案偏离的监查。 • 为临床运营团队提供项目支持，包括参与研究中心可行性评估、主要研究者的选择以及与主 要研究者就项目进行初始的医学讨论。 • 为项目团队或研究者提供方案相关问题的医学培训和支持，包括为项目研究团队编写医学培 训资料、提供相关治疗领域医学知识和方案的培训。 • 出席研究者会议，介绍医学相关的内容（如果需要）。 • 根据项目的需要，参加项目启动会议、研究团队会议和客户会议。 • 为BD团队就新项目提案提供医学支持，必要时约见客户，讨论方案相关的医学问题。 • 与重要领域医学专家建立良好的沟通关系，定期拜访学术领域专家，更新医学进展信息，并 与其维护良好的合作关系。 • 根据本部门的工作需要，撰写本部门相关的SOP。 • 与公司其它部门建立良好的合作关系。 • 根据工作需要，可能需要不定时出差。 • 高效完成直线经理分配的任务。 所需知识、技能和能力 • 具有丰富的临床试验知识背景。 • 了解临床试验相关法规要求，如中国的GCP、ICH-GCP等法规 • 熟练使用 Microsoft Word, PowerPoint 和Excel软件。 • 良好的口头和书面沟通能力（包括能熟练应用英语）。 • 良好的演示技巧和培训技能。 • 具有较强的集体意识和良好的团队合作精神； • 与同事、经理和客户建立和维持有效的工作关系的能力。 学历和经验要求 • 临床医学专业本科及以上学历，或医药相关专业硕士及以上学历。 • 本科学历需有3年及以上的医学顾问或医院临床或临床研究领域相关工作经验； • 硕士学历需有2年及以上的医学顾问或医院临床或临床研究领域相关工作经验； • 博士学历需有1年及以上的医学顾问或医院临床或临床研究领域相关工作经验； • 同等的教育、培训和经验者优先考虑。 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.

Serve as primary contact for investigator sites enrolled in active clinical trials. ​ Address general requests and concerns of internal and external customers.  Assist with training new team members.  May provide support with audit and regulatory inspection.  Responsibilities:  Liaise with investigator sites to notify of alert values, critical values, data clarifications and data revision requests.  Act as primary contact for clinical investigator sites. Resolve issues for study coordinators concerning any aspect of the laboratory services in a timely manner.  Facilitate the flow of information between investigator site and Project Management.  Liaise with internal stakeholders in order to facilitate the laboratory sampling process.  Ensure that Project Management team is made aware of any information that may influence the smooth running of a particular project.  Retrieve voicemail messages concerning supply orders, test or document requests, call backs etc. in a prompt manner.  Assist with training new team members. 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.