Medical, dental and vision coverage

Employee Assistance Programs

Mental health support

Flexible work environment



Time off for leisure, personal time and corporate holidays



Parental leave for birth or adoption 



Paid leave for other life matters (i.e., illness, bereavement, jury duty, military service, etc.)


Retirement and savings plans



Commuter benefits



Life Insurance

SIPP

Work From Home

Large

IQVIA (NYSE:IQV) is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. IQVIA creates intelligent connections across all aspects of healthcare through its analytics, transformative technology, big data resources and extensive domain expertise. IQVIA Connected Intelligence™ delivers powerful insights with speed and agility — enabling customers to accelerate the clinical development and commercialization of innovative medical treatments that improve healthcare outcomes for patients. With approximately 86,000 employees, IQVIA conducts operations in more than 100 countries.

IQVIA is a global leader in protecting individual patient privacy. The company uses a wide variety of privacy-enhancing technologies and safeguards to protect individual privacy while generating and analyzing information on a scale that helps healthcare stakeholders identify disease patterns and correlate with the precise treatment path and therapy needed for better outcomes. IQVIA’s insights and execution capabilities help biotech, medical device and pharmaceutical companies, medical researchers, government agencies, payers and other healthcare stakeholders tap into a deeper understanding of diseases, human behaviors and scientific advances, in an effort to advance their path toward cures.

Science & Healthcare

IQVIA Named to FORTUNE’s 2023 List of “World’s Most Admired Companies,” Ranked #1 in Its Category for the Second Consecutive Year

IQVIA

Accelerate innovation for a healthier world.

You need a Bachelor’s in life sciences, 3 years of clinical research experience, knowledge of GCP/ICH, local regulations, and an understanding of the drug development process.

You will manage site activation, ensure compliance with SOPs, prepare regulatory documents, track approvals, and provide local expertise to project teams while maintaining quality and timelines.

Research & Development

Healthcare

Job Overview Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities. Home Based role requiring German language fluency. Essential Functions * Under general supervision, serve as Single Point of Contact (SPOC) in assigned studies for investigative sites, Site Activation Manager (SAM), Project Management team, and other departments as necessary. * Ensure adherence to standard operating procedures (SOPs), Work Instructions (WIs), quality of designated deliverables and project timelines. * Perform start up and site activation activities according to applicable regulations, SOPs and work instructions. * Distribute completed documents to sites and internal project team members. * Prepare site regulatory documents, reviewing for completeness and accuracy. * Ensure accurate completion and maintenance of internal systems, databases and tracking tools with project specific information. * Review and provide feedback to management on site performance metrics. * Review, establish and agree on project planning and project timelines. Ensure monitoring measures are in place and implement contingency plan as needed. * Inform team members of completion of regulatory and contractual documents for individual sites. * Review, track and follow up the progress, the approval and execution of documents, regulatory, ethics, Informed Consent Form (ICF), and Investigator Pack (IP) release documents, in line with project timelines. * Provide local expertise to SAMs and project team during initial and on-going project timeline planning. * Perform quality control of documents provided by sites. * May have direct contact with sponsors on specific initiatives. Qualifications Bachelor’s Degree in life sciences or a related field and 3 years’ clinical research experience. * In-depth knowledge of clinical systems, procedures, and corporate standards. * Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines. * Knowledge of applicable regulatory requirements, including local regulations, , SOPs and company’s Corporate Standards. * Understanding of regulated clinical trial environment and knowledge of drug development process. 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

Job OverviewPerform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities.Home Based role requiring German language fluency.Essential Functions * Under general supervision, serve as Single Point of Contact (SPOC) in assigned studies for investigative sites, Site Activation Manager (SAM), Project Management team, and other departments as necessary. * Ensure adherence to standard operating procedures (SOPs), Work Instructions (WIs), quality of designated deliverables and project timelines. * Perform start up and site activation activities according to applicable regulations, SOPs and work instructions. * Distribute completed documents to sites and internal project team members. * Prepare site regulatory documents, reviewing for completeness and accuracy. * Ensure accurate completion and maintenance of internal systems, databases and tracking tools with project specific information. * Review and provide feedback to management on site performance metrics. * Review, establish and agree on project planning and project timelines. Ensure monitoring measures are in place and implement contingency plan as needed. * Inform team members of completion of regulatory and contractual documents for individual sites. * Review, track and follow up the progress, the approval and execution of documents, regulatory, ethics, Informed Consent Form (ICF), and Investigator Pack (IP) release documents, in line with project timelines. * Provide local expertise to SAMs and project team during initial and on-going project timeline planning. * Perform quality control of documents provided by sites. * May have direct contact with sponsors on specific initiatives.      QualificationsBachelor’s Degree in life sciences or a related field and 3 years’ clinical research experience. * In-depth knowledge of clinical systems, procedures, and corporate standards. * Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines. * Knowledge of applicable regulatory requirements, including local regulations, , SOPs and company’s Corporate Standards. * Understanding of regulated clinical trial environment and knowledge of drug development process.      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

Regulatory and Start Up Specialist 2 Germany (m/w/d) Home Based - IQVIA

Frankfurt am Main, Hessen, Deutschland

&lt;strong&gt;Job Overview&lt;br&gt;&lt;br&gt;&lt;/strong&gt;Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities.&lt;br&gt;&lt;br&gt;&lt;strong&gt;Home Based role requiring German language fluency. &lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;strong&gt;Essential Functions&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;Under general supervision, serve as Single Point of Contact (SPOC) in assigned studies for investigative sites, Site Activation Manager (SAM), Project Management team, and other departments as necessary.&lt;/li&gt;&lt;li&gt;Ensure adherence to standard operating procedures (SOPs), Work Instructions (WIs), quality of designated deliverables and project timelines.&lt;/li&gt;&lt;li&gt;Perform start up and site activation activities according to applicable regulations, SOPs and work instructions.&lt;/li&gt;&lt;li&gt;Distribute completed documents to sites and internal project team members.&lt;/li&gt;&lt;li&gt;Prepare site regulatory documents, reviewing for completeness and accuracy.&lt;/li&gt;&lt;li&gt;Ensure accurate completion and maintenance of internal systems, databases and tracking tools with project specific information.&lt;/li&gt;&lt;li&gt;Review and provide feedback to management on site performance metrics.&lt;/li&gt;&lt;li&gt;Review, establish and agree on project planning and project timelines. Ensure monitoring measures are in place and implement contingency plan as needed.&lt;/li&gt;&lt;li&gt;Inform team members of completion of regulatory and contractual documents for individual sites.&lt;/li&gt;&lt;li&gt;Review, track and follow up the progress, the approval and execution of documents, regulatory, ethics, Informed Consent Form (ICF), and Investigator Pack (IP) release documents, in line with project timelines.&lt;/li&gt;&lt;li&gt;Provide local expertise to SAMs and project team during initial and on-going project timeline planning.&lt;/li&gt;&lt;li&gt;Perform quality control of documents provided by sites.&lt;/li&gt;&lt;li&gt;May have direct contact with sponsors on specific initiatives.&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;&lt;strong&gt;Qualifications&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;strong&gt;Bachelor’s Degree in life sciences or a related field and 3 years’ clinical research experience&lt;/strong&gt;.&lt;br&gt;&lt;br&gt;&lt;ul&gt;&lt;li&gt;In-depth knowledge of clinical systems, procedures, and corporate standards.&lt;/li&gt;&lt;li&gt;Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines.&lt;/li&gt;&lt;li&gt;Knowledge of applicable regulatory requirements, including local regulations, , SOPs and company’s Corporate Standards.&lt;/li&gt;&lt;li&gt;Understanding of regulated clinical trial environment and knowledge of drug development process.&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;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

Regulatory and Start Up Specialist 2 Germany (m/w/d) Home Based

You need a degree in Life Science or Business, 10-15 years in pharma or CRO, strong analytical skills, leadership abilities, financial acumen, and excellent communication and negotiation skills.

You will lead strategic planning, manage stakeholder relationships, oversee governance activities, support risk management, collaborate with senior leaders, and assist in sales and financial tracking.

Business, Operations & Strategy

Frankfurt

Job Overview: IQVIA, a leading global provider of advanced analytics, technology solutions, and contract research services to the life sciences industry, is seeking a Director/Senior Director Strategy & Business Operations r to join our innovative team. This role will be pivotal in defining and executing the strategy and business operations activities of our Patient and Site Centric Solution Organization within Clinical Operations and ensuring alignment with broader Clinical Operations and R&DS goals. This role will serve as the critical link across multiple departments within Patient and Site Centric Solutions and the broader Clinical Operations, Business Development & Finance Leadership Teams. The Patient and Site Centric Solutions department is made up of a variety of units focused on Clinical Trial Patient Recruitment & Retention, Site Support Services, Decentralized Trials and Site and Patient Insights and Strategic Site Networks. The Strategy & Business Operations role will be responsible for the following main duties: * Business Oversight and Governance: Develop and implement strategic business plans to achieve organizational goals and objectives. * Establish and lead activities related to Business & Operational Governance and be directly responsible for highlighting risks, issues and solutions to support business growth. * Stakeholder Management: Act as Senior Leadership point of contact for internal and external stakeholders. Providing executive reporting and insights and supporting collaboration across R&DS, Commercial & Real World Evidence. * Collaborate with other senior leaders to align business operations with overall company strategy. * Manage risk across the customer portfolio. * Serve as a Senior customer-facing linkage between IQVIA and the customer’s organization, developing relationships and liaising with other customer functional and outsourcing groups as applicable. * Chair relevant Governance Committees as needed * Support Sales, Contracts, and Proposals, and financial tracking and related business matters. * Perform other duties as assigned. Qualifications: * Degree in Life Science, Business Management, or related field required. * 10-15 years of experience in the pharmaceutical, CRO, or related industry, including clinical operations, commercial, and/or alternative operational functions (e.g., business development, data management, project management, laboratory, or an equivalent combination of education, training, and experience. * Excellent communication and interpersonal skills. * Excellent analytical and problem-solving skills. * Demonstrated ability to deliver results to customer expectations. * Strong influencing and negotiation skills. * Excellent matrix and cultural team leadership skills. * Excellent customer service skills. * Sound judgment and decision-making skills. * Strong software and computer skills, including MS Office applications. * Strong financial analysis skills, with a thorough understanding of company margins, pricing strategies, and profitability measures. * Ability to establish and maintain collaborative working relationships with senior management, peers, and customers. 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

Job Overview:IQVIA, a leading global provider of advanced analytics, technology solutions, and contract research services to the life sciences industry, is seeking a Director/Senior Director Strategy & Business Operations r to join our innovative team. This role will be pivotal in defining and executing the strategy and business operations activities of our Patient and Site Centric Solution Organization within Clinical Operations and ensuring alignment with broader Clinical Operations and R&DS goals. This role will serve as the critical link across multiple departments within Patient and Site Centric Solutions and the broader Clinical Operations, Business Development & Finance Leadership Teams.The Patient and Site Centric Solutions department is made up of a variety of units focused on Clinical Trial Patient Recruitment & Retention, Site Support Services, Decentralized Trials and Site and Patient Insights and Strategic Site Networks.The Strategy & Business Operations role will be responsible for the following main duties: * Business Oversight and Governance: Develop and implement strategic business plans to achieve organizational goals and objectives. * Establish and lead activities related to Business & Operational Governance and be directly responsible for highlighting risks, issues and solutions to support business growth. * Stakeholder Management: Act as Senior Leadership point of contact for internal and external stakeholders. Providing executive reporting and insights and supporting collaboration across R&DS, Commercial & Real World Evidence. * Collaborate with other senior leaders to align business operations with overall company strategy. * Manage risk across the customer portfolio. * Serve as a Senior customer-facing linkage between IQVIA and the customer’s organization, developing relationships and liaising with other customer functional and outsourcing groups as applicable. * Chair relevant Governance Committees as needed * Support Sales, Contracts, and Proposals, and financial tracking and related business matters. * Perform other duties as assigned.      Qualifications: * Degree in Life Science, Business Management, or related field required. * 10-15 years of experience in the pharmaceutical, CRO, or related industry, including clinical operations, commercial, and/or alternative operational functions (e.g., business development, data management, project management, laboratory, or an equivalent combination of education, training, and experience. * Excellent communication and interpersonal skills. * Excellent analytical and problem-solving skills. * Demonstrated ability to deliver results to customer expectations. * Strong influencing and negotiation skills. * Excellent matrix and cultural team leadership skills. * Excellent customer service skills. * Sound judgment and decision-making skills. * Strong software and computer skills, including MS Office applications. * Strong financial analysis skills, with a thorough understanding of company margins, pricing strategies, and profitability measures. * Ability to establish and maintain collaborative working relationships with senior management, peers, and customers.      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

Director or Senior Director, Strategy & Business Operations - IQVIA

Director or Senior Director, Strategy & Business Operations

You need a degree in life sciences or healthcare, 1+ year monitoring experience, GCP/ICH knowledge, fluent German (C1), good English, travel flexibility (40-60%), and a driver's license.

You will conduct site visits, support recruitment plans, ensure GCP compliance, track progress, collaborate with sites and clients, and mentor junior team members in clinical research activities.

Join IQVIA as a Clinical Research Associate (m/w/d) home-based throughout Germany in our single sponsor department, and advance your career in clinical research. You’ll enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with one of our clients. Whether you're just starting out or looking to deepen your expertise, this role promises to offer intentional career growth and professional development. With access to world-class training and mentoring, you’ll have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas. 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 at study sites and with client representatives * Depending on client model there might be remote-monitoring, involvement in study start-up processes, specialization on therapeutic area (pharmaceutical product or medical devices) * Mentoring of less experienced team members, support as subject matter expert for specific topics or additional tasks might be included Qualifications: * University Degree in life science or other scientific discipline or apprenticeship in the health care field * Minimum of one year of on-site monitoring experience alternatively an equivalent combination of education, training and 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 * Fluency in German on at least C1 level and a good command of English * Flexibility to travel up to 40-60% 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, accident insurance 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

Join IQVIA as a Clinical Research Associate (m/w/d) home-based throughout Germany in our single sponsor department, and advance your career in clinical research. You’ll enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with one of our clients. Whether you're just starting out or looking to deepen your expertise, this role promises to offer intentional career growth and professional development. With access to world-class training and mentoring, you’ll have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas.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 at study sites and with client representatives * Depending on client model there might be remote-monitoring, involvement in study start-up processes, specialization on therapeutic area (pharmaceutical product or medical devices) * Mentoring of less experienced team members, support as subject matter expert for specific topics or additional tasks might be included      Qualifications: * University Degree in life science or other scientific discipline or apprenticeship in the health care field * Minimum of one year of on-site monitoring experience alternatively an equivalent combination of education, training and 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 * Fluency in German on at least C1 level and a good command of English * Flexibility to travel up to 40-60% 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, accident insurance 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

Clinical Research Associate (m/w/d), Single Sponsor - IQVIA

Join IQVIA as a &lt;strong&gt;Clinical Research Associate&lt;/strong&gt;&lt;strong&gt; (m/w/d) home-based throughout Germany &lt;/strong&gt;in our &lt;strong&gt;single sponsor department&lt;/strong&gt;, and advance your career in clinical research. You’ll enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with one of our clients. Whether you're just starting out or looking to deepen your expertise, this role promises to offer intentional career growth and professional development. With access to world-class training and mentoring, you’ll have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas.&lt;br&gt;&lt;br&gt;&lt;strong&gt;Your responsibilities will include: &lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;Performing site selection, initiation, monitoring and close-out visits&lt;/li&gt;&lt;li&gt;Supporting the development of a subject recruitment plan&lt;/li&gt;&lt;li&gt;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&lt;/li&gt;&lt;li&gt;Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution&lt;/li&gt;&lt;li&gt;Collaborating with experts at study sites and with client representatives&lt;/li&gt;&lt;li&gt;Depending on client model there might be remote-monitoring, involvement in study start-up processes, specialization on therapeutic area (pharmaceutical product or medical devices) &lt;/li&gt;&lt;li&gt;Mentoring of less experienced team members, support as subject matter expert for specific topics or additional tasks might be included&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;&lt;strong&gt;Qualifications: &lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;University Degree in life science or other scientific discipline or apprenticeship in the health care field&lt;/li&gt;&lt;li&gt;Minimum of one year of on-site monitoring experience alternatively an equivalent combination of education, training and experience&lt;/li&gt;&lt;li&gt;Knowledge of applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines&lt;/li&gt;&lt;li&gt;Strong written and verbal communication skills, attention to detail and ability to work in a fast pace environment&lt;/li&gt;&lt;li&gt;Fluency in German on at least C1 level and a good command of English&lt;/li&gt;&lt;li&gt;Flexibility to travel up to 40-60% of working time&lt;/li&gt;&lt;li&gt;Driver’s license class B&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;&lt;strong&gt;What you can expect: &lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;Resources that promote your career growth&lt;/li&gt;&lt;li&gt;Leaders that support flexible work schedules&lt;/li&gt;&lt;li&gt;Programs to help you build your therapeutic knowledge&lt;/li&gt;&lt;li&gt;Dynamic work environments that expose you to new experiences&lt;/li&gt;&lt;li&gt;Home-office, company car, accident insurance and more&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;Whatever your career goals, we are here to ensure you get there!&lt;br&gt;&lt;br&gt;&lt;strong&gt;Please apply with your English CV and motivation letter.&lt;br&gt;&lt;br&gt;&lt;/strong&gt;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

Clinical Research Associate (m/w/d), Single Sponsor

Germany

You must be fluent in Japanese and English, hold a Bachelor's degree, have 3 years of experience, and possess strong communication, problem-solving, and teamwork skills, plus MS Office proficiency.

You will manage project timelines, budgets, and reporting, coordinate with teams, present project updates, and ensure compliance with processes while tracking deliverables and invoicing.

Reading

<div>Join our dynamic Translation team in IQVIA and be part of a global organization that values innovation, collaboration, and professional growth. We are looking for a motivated and talented Senior Content Design Specialist who is a native Japanese speaker to support our multilingual desktop publishing (DTP) projects.
Location: anywhere in Europe
Job Overview 
Manages the operational aspects of projects and programs. Will ensure that all project work is completed in accordance with SOPs, policies and practices.
Essential Functions<ul><li>
Create, track and report on project timelines</li><li>
Manage project budgets and approval of invoices</li><li>
Produce and distribute status, tracking and financial reports for internal and external team members and senior management.</li><li>
Prepare and present project information at internal and external meetings.</li><li>
May be assigned responsibility for sub-projects or specific components of the project or program</li><li>
May participate in proposal development and sales/proposal presentations</li><li>
Coordinate with other project resources within and outside the organization.</li><li>
Provide input into project proposals and RFPs.</li><li>
Ensure that work is conducted in compliance with standard processes, policies and procedures and meets project timeline metrics.</li><li>
Serve as a backup contact for internal Project Managers.</li><li>
Identify and negotiate out of scope project work</li><li>
Responsibility for financial reporting on the project including tracking deliverables and invoicing</li><li>
Meet with team members on a regular basis regarding project tasks to ensure project milestones are met.</li><li>
Partner with other Project Managers to develop and implement process improvements</li></ul>
Qualifications<ul><li>
Fluent in Japanese and English</li><li>
Bachelor's Degree Req</li><li>
3 years of related experience Req Or</li><li>
Equivalent combination of education, training and experience Req</li><li>
Strong communication and interpersonal skills</li><li>
Good problem solving skills</li><li>
Demonstrated ability to deliver results to the appropriate quality and timeline metrics</li><li>
Good teamwork skills</li><li>
Excellent customer service skills</li><li>
Ability to work under limited direction</li><li>
Strong software and computer skills, including MS Office applications</li><li>
Ability to establish and maintain effective working relationships with coworkers, managers and clients</li></ul>
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</div>

Join our dynamic Translation team in IQVIA and be part of a global organization that values innovation, collaboration, and professional growth. We are looking for a motivated and talented Senior Content Design Specialist who is a native Japanese speaker to support our multilingual desktop publishing (DTP) projects.
Location: anywhere in Europe
Job Overview
Manages the operational aspects of projects and programs. Will ensure that all project work is completed in accordance with SOPs, policies and practices.
Essential Functions
Create, track and report on project timelines
Manage project budgets and approval of invoices
Produce and distribute status, tracking and financial reports for internal and external team members and senior management.
Prepare and present project information at internal and external meetings.
May be assigned responsibility for sub-projects or specific components of the project or program
May participate in proposal development and sales/proposal presentations
Coordinate with other project resources within and outside the organization.
Provide input into project proposals and RFPs.
Ensure that work is conducted in compliance with standard processes, policies and procedures and meets project timeline metrics.
Serve as a backup contact for internal Project Managers.
Identify and negotiate out of scope project work
Responsibility for financial reporting on the project including tracking deliverables and invoicing
Meet with team members on a regular basis regarding project tasks to ensure project milestones are met.
Partner with other Project Managers to develop and implement process improvements
Qualifications
Fluent in Japanese and English
Bachelor's Degree Req
3 years of related experience Req Or
Equivalent combination of education, training and experience Req
Strong communication and interpersonal skills
Good problem solving skills
Demonstrated ability to deliver results to the appropriate quality and timeline metrics
Good teamwork skills
Excellent customer service skills
Ability to work under limited direction
Strong software and computer skills, including MS Office applications
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

Senior Content Design Specialist with Japanese - IQVIA

United Kingdom

Portugal

Netherlands

Ireland

Italy

Spain

France

Switzerland

Senior Content Design Specialist with Japanese

You should have 2+ years of relevant experience, knowledge of clinical trials, strong IT skills, excellent interpersonal abilities, and fluent German.

You will coordinate clinical studies, ensure patient well-being, manage study documentation, assist in patient recruitment, and collaborate with monitors on study-related issues.

Oldenburg

Sind Sie auf der Suche nach einer Chance oder einer neuen Herausforderung in der klinischen Forschung? Möchten Sie für ein branchenführendes Unternehmen arbeiten? IQVIA sucht derzeit nach einem/r Clinical Research Coordinator / Study Nurse (m/w/d), die/der an einem Zentrum in Oldenburg die Durchführung einer klinischen Studie unterstützt. Diese Teilzeitstelle (24 Stunden pro Woche) mit Start per sofort ist für ca. 3 Monate zu besetzen. Zu den täglichen Aufgaben gehören: * Koordinierung klinischer Forschungsstudien und Aufrechterhaltung eines sicheren Studienumfelds gemäß den Gesundheits- und Sicherheitsrichtlinien unter der Leitung und Delegation des Principal Investigators * Sicherstellung des Wohlergehens der PatientInnen, Eingehen auf deren Belange bei gleichzeitiger Gewährleistung der höchsten Qualität * Betreuung der PatientInnen und Unterstützung des Personals bei administrativen Aufgaben * Pflege von Studienprotokollen, Fallberichtsformularen (CRFs), elektronischen Datenerfassungssystemen (EDC) und anderen Studiendokumenten auf dem neuesten Stand * Planung und Koordinierung der logistischen Aktivitäten für Studienverfahren gemäß dem Studienprotokoll * Durchführung der klinischen Vorbereitungen für die Studie, einschließlich der Beschriftung von Probenentnahmeröhrchen und -behältern, der Inventarisierung des erforderlichen Materials und der Einrichtung oder Behebung von Problemen mit der Ausrüstung und/oder der Studie * Dateneingabe, Überprüfung der Datenqualität und Beantwortung von Fragen * Unterstützung bei der Aufnahme von PatientInnen in die Studie durch Rekrutierung, Screening und Einweisung gemäß dem Studienprotokoll * Sammeln, Erfassen und Berichten klinischer Daten und Befunde in angemessener Weise in CRFs und Zusammenarbeit mit dem Prüfarzt über studienbezogene unerwünschte Ereignisse und schwerwiegende unerwünschte Ereignisse gemäß dem Studienprotokoll * Koordinierung mit dem Studienmonitor bei Studienproblemen und effektive Beantwortung der vom Monitor gestellten Fragen. Wir suchen Kandidaten mit den folgenden Fähigkeiten und Erfahrungen: * Mindestens zwei Jahre einschlägige Erfahrung; oder eine gleichwertige Kombination aus medizinischer Ausbildung, Schulung und Erfahrung * Kenntnisse über klinische Studien, kombiniert mit fundierten Kenntnissen der abteilungs-, protokoll- und studienspezifischen Arbeitsabläufe, Einverständniserklärungen und Studienpläne * Ausgeprägte IT-Kenntnisse, geübt im Umgang mit MS Windows und Office-Anwendungen wie Access, Outlook, Excel und Word * Ausgezeichnete zwischenmenschliche Fähigkeiten mit der Fähigkeit, effektive Arbeitsbeziehungen aufzubauen und zu pflegen * Sehr gute Deutschkenntnisse in Wort und Schrift 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

Sind Sie auf der Suche nach einer Chance oder einer neuen Herausforderung in der klinischen Forschung? Möchten Sie für ein branchenführendes Unternehmen arbeiten? IQVIA sucht derzeit nach einem/r Clinical Research Coordinator / Study Nurse (m/w/d), die/der an einem Zentrum in Oldenburg die Durchführung einer klinischen Studie unterstützt.Diese Teilzeitstelle (24 Stunden pro Woche) mit Start per sofort ist für ca. 3 Monate zu besetzen.Zu den täglichen Aufgaben gehören: * Koordinierung klinischer Forschungsstudien und Aufrechterhaltung eines sicheren Studienumfelds gemäß den Gesundheits- und Sicherheitsrichtlinien unter der Leitung und Delegation des Principal Investigators * Sicherstellung des Wohlergehens der PatientInnen, Eingehen auf deren Belange bei gleichzeitiger Gewährleistung der höchsten Qualität * Betreuung der PatientInnen und Unterstützung des Personals bei administrativen Aufgaben * Pflege von Studienprotokollen, Fallberichtsformularen (CRFs), elektronischen Datenerfassungssystemen (EDC) und anderen Studiendokumenten auf dem neuesten Stand * Planung und Koordinierung der logistischen Aktivitäten für Studienverfahren gemäß dem Studienprotokoll * Durchführung der klinischen Vorbereitungen für die Studie, einschließlich der Beschriftung von Probenentnahmeröhrchen und -behältern, der Inventarisierung des erforderlichen Materials und der Einrichtung oder Behebung von Problemen mit der Ausrüstung und/oder der Studie * Dateneingabe, Überprüfung der Datenqualität und Beantwortung von Fragen * Unterstützung bei der Aufnahme von PatientInnen in die Studie durch Rekrutierung, Screening und Einweisung gemäß dem Studienprotokoll * Sammeln, Erfassen und Berichten klinischer Daten und Befunde in angemessener Weise in CRFs und Zusammenarbeit mit dem Prüfarzt über studienbezogene unerwünschte Ereignisse und schwerwiegende unerwünschte Ereignisse gemäß dem Studienprotokoll * Koordinierung mit dem Studienmonitor bei Studienproblemen und effektive Beantwortung der vom Monitor gestellten Fragen.      Wir suchen Kandidaten mit den folgenden Fähigkeiten und Erfahrungen: * Mindestens zwei Jahre einschlägige Erfahrung; oder eine gleichwertige Kombination aus medizinischer Ausbildung, Schulung und Erfahrung * Kenntnisse über klinische Studien, kombiniert mit fundierten Kenntnissen der abteilungs-, protokoll- und studienspezifischen Arbeitsabläufe, Einverständniserklärungen und Studienpläne * Ausgeprägte IT-Kenntnisse, geübt im Umgang mit MS Windows und Office-Anwendungen wie Access, Outlook, Excel und Word * Ausgezeichnete zwischenmenschliche Fähigkeiten mit der Fähigkeit, effektive Arbeitsbeziehungen aufzubauen und zu pflegen * Sehr gute Deutschkenntnisse in Wort und Schrift      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

Clinical Research Coordinator / Study Nurse (m/w/d) - Oldenburg - IQVIA

Sind Sie auf der Suche nach einer Chance oder einer neuen Herausforderung in der klinischen Forschung? Möchten Sie für ein branchenführendes Unternehmen arbeiten? IQVIA sucht derzeit nach einem/r Clinical Research Coordinator / Study Nurse (m/w/d), die/der an einem Zentrum in Oldenburg die Durchführung einer klinischen Studie unterstützt.&lt;br&gt;&lt;br&gt;Diese Teilzeitstelle (24 Stunden pro Woche) mit Start per sofort ist für ca. 3 Monate zu besetzen.&lt;br&gt;&lt;br&gt;Zu den täglichen Aufgaben gehören:&lt;br&gt;&lt;br&gt;&lt;br&gt;&lt;ul&gt;&lt;li&gt;Koordinierung klinischer Forschungsstudien und Aufrechterhaltung eines sicheren Studienumfelds gemäß den Gesundheits- und Sicherheitsrichtlinien unter der Leitung und Delegation des Principal Investigators&lt;/li&gt;&lt;li&gt;Sicherstellung des Wohlergehens der PatientInnen, Eingehen auf deren Belange bei gleichzeitiger Gewährleistung der höchsten Qualität&lt;/li&gt;&lt;li&gt;Betreuung der PatientInnen und Unterstützung des Personals bei administrativen Aufgaben&lt;/li&gt;&lt;li&gt;Pflege von Studienprotokollen, Fallberichtsformularen (CRFs), elektronischen Datenerfassungssystemen (EDC) und anderen Studiendokumenten auf dem neuesten Stand&lt;/li&gt;&lt;li&gt;Planung und Koordinierung der logistischen Aktivitäten für Studienverfahren gemäß dem Studienprotokoll&lt;/li&gt;&lt;li&gt;Durchführung der klinischen Vorbereitungen für die Studie, einschließlich der Beschriftung von Probenentnahmeröhrchen und -behältern, der Inventarisierung des erforderlichen Materials und der Einrichtung oder Behebung von Problemen mit der Ausrüstung und/oder der Studie&lt;/li&gt;&lt;li&gt;Dateneingabe, Überprüfung der Datenqualität und Beantwortung von Fragen&lt;/li&gt;&lt;li&gt;Unterstützung bei der Aufnahme von PatientInnen in die Studie durch Rekrutierung, Screening und Einweisung gemäß dem Studienprotokoll&lt;/li&gt;&lt;li&gt;Sammeln, Erfassen und Berichten klinischer Daten und Befunde in angemessener Weise in CRFs und Zusammenarbeit mit dem Prüfarzt über studienbezogene unerwünschte Ereignisse und schwerwiegende unerwünschte Ereignisse gemäß dem Studienprotokoll&lt;/li&gt;&lt;li&gt;Koordinierung mit dem Studienmonitor bei Studienproblemen und effektive Beantwortung der vom Monitor gestellten Fragen.&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;Wir suchen Kandidaten mit den folgenden Fähigkeiten und Erfahrungen:&lt;br&gt;&lt;br&gt;&lt;br&gt;&lt;ul&gt;&lt;li&gt;Mindestens zwei Jahre einschlägige Erfahrung; oder eine gleichwertige Kombination aus medizinischer Ausbildung, Schulung und Erfahrung &lt;/li&gt;&lt;li&gt;Kenntnisse über klinische Studien, kombiniert mit fundierten Kenntnissen der abteilungs-, protokoll- und studienspezifischen Arbeitsabläufe, Einverständniserklärungen und Studienpläne&lt;/li&gt;&lt;li&gt;Ausgeprägte IT-Kenntnisse, geübt im Umgang mit MS Windows und Office-Anwendungen wie Access, Outlook, Excel und Word&lt;/li&gt;&lt;li&gt;Ausgezeichnete zwischenmenschliche Fähigkeiten mit der Fähigkeit, effektive Arbeitsbeziehungen aufzubauen und zu pflegen&lt;/li&gt;&lt;li&gt;Sehr gute Deutschkenntnisse in Wort und Schrift&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;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&lt;br&gt;&lt;br&gt;