IQVIA

Clinical Research Associate 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 and International Conference on Harmonization guidelines Managing progress by tracking regulatory submissions, recruitment, case report form completion, and data query resolutions Collaborating with experts at study sites and with client representatives Qualifications: University degree in scientific discipline or health care At least 2 year of experience as a Clinical Research Associate. Very good computer skills including MS Office Excellent command of Slovak and English language- Slovakia based. Organizational, time management and problem-solving skills Ability to establish and maintain effective working relationships with coworkers, managers, and clients Flexibility to travel 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 Excellent working environment in a stabile, international, reputable company 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 €26,000.00 - €59,400.00. 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.

Job Overview Details and sell over the counter products to pharmacies at agreed prices and deal levels to achieve and maintain defined average daily call rate, orders & value/volumes, whilst adhering to the telesales call flow model.Grow the business on territory by brand over a set period, ensuring personal and team targets are achieved, whilst also developing new business.Provide additional support by telephone to clients during specific sales drives.Produce emails & flyers and promotional material on set drive lines to assist in target achievement.Ensure that daily administration is completed accurately, and that advice of call emails are sent out to pharmacies one week in advance of the proposed telesales call.Complete all order processing and recording efficiently and accurately.Monitor your own sales performance to ensure that call rates and standards are met and maintained.Utilise the company’s CRM system to analyse your sales performance and react to sales trends.Liaise with the Sales Support Manager to ensure that call rates and standards are met and maintained.Carry out any other reasonable task in relation to the overall job, as required.Develop and maintain a current knowledge of the industry.Career Experience Minimum of 2 years telephone account management experience, in a similar fast-paced and target driven environment is essential.Previous experience of working in the FMCG industry is desirable.Previous experience of utilising a CRM system in order to load sales results and run basic reports is preferred.Qualifications A good standard of general education, including Maths and English.Required Skills The ability to manage your own territory and customer base in order to plan your calls effectively and achieve designated KPI’s.The ability to communicate confidently with external customers in order to detail the features and benefits of products and to handle objections.The ability to negotiate with buyers toThe ability to utilise Excel to a basic level in order to maintain basic template formulas and formatting and analyse sales dataThe ability to utilise a CRM system effectively in order to  extract relevant data to support your analysis and recommendationsThe ability to utilise PowerPoint to a basic level in order to maintain handover files.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.

Clinical Trial Management & Central Trial Oversight (FSP Model) Home Based Remote Role - East Coast  Role Overview IQVIA is seeking an accomplished Senior Project Lead / Associate Director, Clinical Trial Management to provide centralized, global clinical trial oversight within our Functional Service Provider (FSP) model. This role partners closely with a Global Trial Leadership and cross-functional stakeholders to ensure the successful planning, execution, and delivery of complex clinical trials across regions and vendors. You will lead Study Management Teams (SMTs), oversee country and site-facing activities, and ensure trials are conducted with the highest standards of quality, compliance, and inspection readiness—from start-up through close-out. This role is ideal for a senior clinical operations professional who thrives in a matrixed, global environment and is ready to influence strategy, mentor teams, and drive operational excellence. Key Responsibilities Global & Regional Trial Leadership Lead and coordinate global and regional clinical trial management activities for internally managed and outsourced studies.Serve as a core member of the Trial Team, partnering with Global Leadership to deliver operational strategy and execution.Act as primary point of contact for country, regional, and functional stakeholders within Clinical Development Operations.Function as backup or first point of contact in the absence of the Global Leadership.Central Trial Oversight & Execution Drive trial delivery across the full lifecycle: feasibility, site selection, start-up, execution, and close-out.Ensure milestones, timelines, and deliverables are met and transparently communicated.Maintain real-time trial oversight through dashboards, reports, and issue tracking.Act as the central subject matter expert for assigned protocols.Vendor & Partner Management Provide oversight of CROs and global vendors supporting site-facing activities, including:IWRS/IVRSCentral LaboratoryePRO/eCOAImagingTranslation and printingAncillary supplies and investigator meetingsReview and approve vendor deliverables, invoices, and spend.Ensure vendor performance aligns with trial plans, budgets, and quality expectations.Quality, Compliance & Inspection Readiness Ensure continuous inspection readiness in accordance with ICH-GCP, applicable regulations, and sponsor SOPs.Lead or contribute to CAPA development and resolution.Support Health Authority inspections, internal audits, and quality reviews.Partner with Quality & Compliance stakeholders to ensure effective oversight.Enrollment, Feasibility & Risk Management Lead feasibility activities and provide data-driven recommendations.Establish and track regional enrollment commitments, ensuring alignment with projections.Ensure robust recruitment and contingency plans are in place.Proactively identify risks, escalate issues, and drive resolution.Documentation, Systems & Trial Deliverables Oversee trial documentation, filing, archiving, and retention.Create, review, and maintain trial-specific documents, including:Monitoring GuidelinesInformed Consent FormsIMP and blinding documentationFeasibility and site selection materialsSupport HA/EC/IRB submissions with required central documents.Coordinate data cleaning activities to support timely database lock.Leadership, Mentorship & Continuous Improvement Lead teams across projects or programs.Provide coaching and mentoring to less experienced team members.Lead or participate in special initiatives, task forces, and process improvement efforts.Contribute innovative ideas to enhance operational efficiency and quality across the FSP partnership.Level Differentiation  (Base Level) Independently manages complex trials with limited oversight.Demonstrates strong operational leadership and stakeholder management.Owns central trial oversight activities and delivers consistent, high-quality results. (Advanced Level) Leads program-level or high-impact trials with increased complexity.Manages and mentors multiple team members across insourced and outsourced studies.Serves as a Therapeutic Area Expert or Functional Champion, influencing strategy and best practices.Proactively identifies and resolves budget, resourcing, and operational risks.Qualifications & Experience Education Bachelor’s degree (or equivalent) in Life Sciences (e.g., Biology, Chemistry, Nursing, Pharmacy).Experience Base:6+ years of clinical trial management experience in pharma and/or CRO environments.Advanced:8+ years of clinical trial management experience, including leadership of complex global studies.Proven experience managing trials from start-up through database lock and close-out.Experience coordinating global, virtual teams in a large matrix environment for 2–3+ years.Therapeutic area experience required.Technical & Professional Skills Deep knowledge of ICH-GCP, regulatory requirements, and clinical operations best practices.Strong project management, planning, and risk mitigation skills.Demonstrated ability to manage country and vendor budgets, including OOPs and cost drivers.Experience with CTMS, TMF systems, and Microsoft applications.Monitoring experience preferred (or equivalent central monitoring/data management experience).Strong analytical, decision-making, and communication skills.Fluent in English; local language proficiency as required.Willingness to travel as needed.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 $93,100.00 - $285,500.00. 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.

Graphic Designer – Life Sciences Role Overview We are seeking a creative and detail-oriented Graphic Designer to design and develop high-quality digital and print assets for global life sciences/pharmaceutical clients. The role requires strong visual storytelling skills and hands-on expertise across Adobe and video design tools. Key Responsibilities Creative Design & Asset Development Design digital assets: banners, emailers, infographics, visual aids, and social creativesDevelop multimedia content: 2D/3D videos, animations, and motion graphicsCreate print assets: brochures, leave-behinds, magazines, and promotional materialsTranslate brief requirements into visually compelling, brand-compliant designsLife Sciences Content Adaptation Work with medical, marketing, and content teams to convert complex scientific content into easy-to-understand visual formatsEnsure all creatives adhere to brand guidelines and compliance standards (MLR awareness preferred)Stakeholder Collaboration Liaise with internal teams and client stakeholders to understand requirements, iterate designs, and deliver on timelinesIncorporate feedback effectively while maintaining design quality and consistencyProduction & Quality Control Prepare final files for digital publishing and print productionEnsure accuracy, consistency, and high-quality output across formatsRequired Skills & Experience 2–4 years of experience in graphic design (agency or healthcare/life sciences preferred)Strong portfolio demonstrating digital + print + video design workAdvanced level of english.Tools Expertise: Adobe Creative Suite:Photoshop, Illustrator, InDesign (mandatory)Video/Motion tools (any of):After Effects, Premiere Pro, Blender, or similar toolsDesign Capabilities: Strong understanding of layout, typography, color theory, and brandingExperience in infographics, visual storytelling, and multimedia designWorking knowledge of 2D/3D design and animation conceptsPreferred Qualifications Experience working with pharmaceutical / healthcare clientsFamiliarity with MLR processes and regulated content environmentsBasic understanding of UX/UI principles for digital formatsKey Traits High attention to detail and accuracyAbility to manage multiple projects under tight timelinesStrong communication and stakeholder management skillsCreative thinker with a problem-solving mindsetIQVIA 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 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 research Keep growing with an organization that encourages and invests in continuous professional and personal development Apply your business and leadership skills in an entrepreneurial and multi-disciplinary team Continue challenging yourself by addressing the toughest client issues, working across multiple geographies and solutions in a dynamic and crucial field for the industry Make a difference to patients by enabling the successful approval or launch of new treatments with features that are truly patient-centric Role Overview Within PCS, the Qualitative Research Specialty (QRS) delivers scientifically rigorous qualitative research to inform clinical development, regulatory strategy, and healthcare decision‑making. We are seeking an Associate Principal / Principal to join the QRS team, based in the UK or Europe, with flexibility for remote or hybrid working. This role blends scientific leadership, consulting delivery, and people development. The exact level (Associate Principal or Principal) will depend on experience and demonstrated leadership scope. The role is positioned between project‑level scientific leadership and broader practice‑level contribution, with increasing responsibility for client leadership, methodological excellence, business development support, and capability building across the qualitative community. The role has a particular emphasis on generating and applying patient experience data to inform COA development, evaluation, and use within clinical and regulatory contexts. Key Responsibilities Scientific & Consulting Leadership Act as a subject matter expert (SME) in qualitative research, providing expert guidance on study design, methodological approaches, and interpretation of patient experience data, translating findings into evidence that informs COA strategy, endpoint development, and broader clinical and commercial decision-making  across a portfolio of projects spanning in-trial settings, observational studies, and standalone research programmes. Lead the design, execution, and delivery of high‑quality qualitative research, including examining burden of disease, evaluating content validity of PROs and other COAs, and the development or modification of COA measures, ensuring scientific rigour, methodological appropriateness, and alignment with regulatory, publication, and client expectations. Identify, evaluate, and apply innovative qualitative methods, including AI-enabled approaches, to enhance study design, data collection, and analysis while maintaining scientific rigour. Lead the review and testing of emerging qualitative research and analysis methods and contribute to the evidence base for their use at PCS. Provide senior scientific input into qualitative analysis plans, interpretation of patient experience data, and development of reports and client‑facing deliverables. Project & Client Management Act as a trusted scientific and strategic advisor to clients, contributing to discussions on research design, patient‑centred endpoints, and evidence needs. Take ownership for overall project quality, delivery, and client satisfaction, ensuring projects remain on track and aligned with scope, timelines, and objectives. Lead or oversee multiple qualitative consulting projects, ensuring delivery on time, within scope, and to budget. Serve as a primary or senior point of contact for clients, building strong, long‑term relationships through meetings, workshops, and ongoing collaboration. Anticipate project risks and proactively resolve issues, escalating as needed while maintaining client confidence. Support proposal development, including methodological input, budgeting, timelines, and bid integrity. Practice Development & Business Growth Identify opportunities for follow‑on work, methodological innovation (including the scaling of innovative and AI-enabled qualitative approaches), and expansion of qualitative service offerings within PCS. Contribute to thought leadership, including development of best practices, internal guidance, and externally facing scientific content (e.g. abstracts, presentations, publications). Support business development activities by providing subject‑matter expertise and mentoring others in client and proposal engagement. Quality, Standards & Capability Building Contribute to the development, refinement, and implementation of qualitative research standards, templates, SOPs, and training materials. Oversee and contribute to the qualification and ongoing development of qualitative researchers, including assessment of interview moderators. Support consistency and quality across qualitative projects, working collaboratively with global qualitative leaders (Global Qualitative Research Speciality Leads, Delivery & Capabilities; Innovation & Professional Development). Provide scientific review and guidance to ensure best practice in qualitative data collection, analysis, and reporting. People Development & Collaboration Mentor and coach junior and mid‑level staff, providing scientific guidance, project oversight, and developmental feedback. Line manage and formally coach a small number of staff, supporting their scientific development, performance, and career progression, depending on level and business need. Actively contribute to the global PCS qualitative community, supporting recruitment, onboarding, and knowledge‑sharing initiatives. Foster a collaborative, inclusive, and high‑performing team culture across geographies. About You Essential Qualifications & Experience PhD in a relevant discipline (e.g. psychology, anthropology, sociology, public health, health sciences) or a Master’s degree with substantial consulting or additional experience. 5-8 years professional experience in consulting within the pharmaceutical industry. Demonstrated expertise in designing, conducting, and analyzing qualitative research in healthcare settings. Familiar with designing and leading qualitative research consistent with Patient-Focused Drug Development guidance published by the US FDA. Experience working in roles generating or communicating robust clinical data suitable for submission to regulatory bodies, payers or for publication; including exposure to the development and validation of COAs. Experience using qualitative data analysis software (e.g., ATLAS.ti, MAXQDA, NVivo) to support efficient and rigorous coding, analysis and management of qualitative data. Experience working in consulting or a CRO environment, managing multiple complex projects and senior client stakeholders. Strong understanding of qualitative methods, analytical approaches, and reporting standards suitable for regulatory, payer, or publication contexts. Demonstrable analytical, interpretative, and problem-solving skills, with the ability to learn quickly, adapt, and apply new knowledge. Strong capability in juggling priorities so that deadlines are met while retaining consistently high-quality outcomes. Excellent written and verbal communication skills, including client presentations, workshops, and scientific writing. Ability to manage and collaborate with individuals at all levels within the organization and build relationships while working remotely. Desirable Experience (depending on level) Experience contributing to regulatory‑focused research (e.g. clinical trials, endpoint development, patient experience studies). Track record of publications, abstracts, or conference presentations. Experience with cross-cultural or multilingual research design. Experience contributing to proposal development and business growth. Formal people management or coaching experience. Core Competencies Scientific curiosity and commitment to methodological excellence. Strong project and stakeholder management skills. Ability to translate complex qualitative insights into clear, actionable narratives for clients. Collaborative mindset with the confidence to provide senior‑level input and challenge constructively. Excellent organizational skills and ability to balance competing priorities. Strong client focus, including the ability to lead senior discussions to uncover underlying needs, shape strategic research approaches, and support the growth of client accounts. Execution excellence, with accountability for high-quality, on-time delivery, proactive risk mitigation and oversight of project delivery. People leadership, demonstrated through mentoring, coaching, and supporting the development of qualitative researchers Practical Details Location: UK or Europe Working model: Remote or hybrid (office/home‑based) Travel: Occasional travel expected Language: Fluency in English (spoken and written) Eligibility: Right to live and work in the recruiting country This role offers the opportunity to play a visible and influential part in advancing qualitative patient‑centred research, while shaping the next generation of scientific and consulting talent within PCS. As part of this role, the successful candidate will join the QRS within PCS. The QRS is a globally connected team of qualitative subject‑matter experts located across Europe, the Americas, bringing deep methodological expertise and diverse healthcare system perspectives to client projects. The QRS has responsibility for the delivery of high‑quality qualitative research, the development and mentoring of qualitative researchers, and the advancement of innovative methods and best practices across the broader Patient Centred Outcomes organization. Level and scope will be tailored to Associate Principal or Principal based on experience, leadership breadth, and business needs. 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.

Provides data management support, oversight and/or accountability for one or more clinical trials.Take the lead with the trial customer(s) and other internal and external partners to establish, align and confirm data management expectationsCreating, planning, and tracking content, format, quality, and timing of data management deliverables, including, but not limited to, CRF, data review plan, QC plan, oversight plan, database release plan, final datasets, submission plan and archival.With the trial customer and other functional partners: – Gathers content and integration requirements for eCRF and other data collection tools.Establishes conventions and quality expectations for clinical data.Establishes expectations for dataset content and structure.Set timelines and follow-up to ensure delivery of all Data Management milestones.Performs trial level oversight controls, as appropriate, as described in the oversight plan, QC process and work instructions with minimal DML direction.Creates clinical data management documents (including submission package) ensuring appropriate quality, scientific content, organization, clarity, accuracy, format, and consistency. Ensures compliance with regulatory guidelines and the documentation matrix.Ensures real-time inspection readiness of all Data Management deliverables for the trial; Participate in Regulatory Agency and audits, as necessary.Helps plan, create and track content, format, quality, and timing of data management deliverables, including, but not limited to, Case Report Form, data review plan, QC plan, oversight plan, database release plan, final datasets, submission plan and archival. Ensures deliverables are on time.Participates in the assigned clinical working group(s) to ensure that Data Management and Therapeutic Area trial needs and deliverables are met.Helps Identify and communicate lessons learned, best practices and frequently asked questions at the trial level.Presents and trains at investigator and monitor meetingsEducation/Experience BS/BA degree or higher preferably in Health Sciences, or BS/BA degree or higher with professional clinical experience/exposure.5 years Data management experience.3 years lead/co-lead experienceVendor Management experienceRAVE experienceThis role is not eligible for UK visa sponsorship 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.

Do you want to make an impact on the future of healthcare through data and consultancy? IQVIA is a global leader in data, technology and advanced analytics within the healthcare sector. As part of our Healthcare team, we help hospitals to strike the optimal balance between demand for care, capacity and quality, using data-driven insights and practical solutions. Your role As a Capacity Management Consultant, you will work at the intersection of data, consultancy and product development. You will support hospitals with analyses and advice, whilst contributing to the development of innovative tools and solutions. Responsibilities Consultancy & Capacity Management Delivering projects relating to capacity and care processesAnalysing data (planning, throughput, occupancy) and identifying areas for improvementAdvising stakeholders at all levelsTranslating data into concrete, actionable insightsBridge between market, data and product Translating customer needs into product requirementsContributing to product development and innovationsSupporting sales with use cases, demos and quotationsMethodology & development Standardising approaches and toolsContributing to scalable solutions and dashboardsProject & change management Guiding change processesMonitoring quality, timing and impactProfile Min. 3 years’ relevant experienceStrong analytical skills, experience with complex datasetsAffinity with healthcare and capacity managementStrong communication and stakeholder management skillsIndependent, organised and results-orientedGood knowledge of Excel and PowerPointVery good knowledge of Dutch and French, and willing to travel within BelgiumWhat does IQVIA offer? A role with real impact in the healthcare sectorVaried work: consultancy and product developmentOpportunities for initiative and growthCollaboration with an experienced teamCompetitive salary package with benefitsIQVIA 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 • 作为研究团队成员，遵照法规要求、商定的工作范围、适用的SOP、工作授权和试验方案，在 研究中心进行工作。 • 协助研究者完成可行性调查问卷和回收问卷。 • 推动研究中心启动工作：协助研究中心筛选访视，协助及时提交文件到伦理委员会进行审批 和试验用药品的发放，协助研究中心启动访视。 • 协助研究者进行受试者筛选和入组研究。 • 得到研究者授权后，根据法规和GCP的要求，协助研究者顺利完成方案要求的随访和步骤：如 制定计划、清点核对药品和其他协调工作。 • 在研究中心协助研究者管理试验用药品、研究物资和实验室样本。 • 在商定的工作范围内，参加研究者会、监查访视、稽查和其他会议。 • 协助研究者归档研究资料，并提交至伦理委员会或其他权威机构。 • 准确地将原始文件中的数据填写到病例报告表，并协助query的解答。 • 推动研究中心关闭：协助研究中心关闭访视、试验用药品和研究资料的回收，以及研究资料 的归档。 • 创建和维护日常工作报告和其他工作文件。 • 根据工作需要，可能需要不定时出差或暂时借调至其他城市。 • 完成分配的其他任务。 所需知识、技能和能力 • 了解临床研究的基本知识和适用的法规要求。 • 熟悉医学术语。 • 良好的人际沟通及组织能力。 • 熟练使用微软办公软件。 • 熟练的中文说写能力。要求基本的英语水平。 • 能独立完成任务，根据优先级选择重点，寻找资源，能解决问题，适应在团队中工作。 • 能够严格保密。 学历和经验要求 • 大专及以上学历，临床医学、药理学、护理、卫生保健或其他医学相关专业。 • 未满1年的临床究协调员经验。 • 临床研究或医药行业工作/实习经验。 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.

根据试验方案、合同规定的工作范围、SOP和GCP的要求进行研究中心筛选、启动、监查和关闭访视。 可同时负责多个方案、研究中心和治疗领域内的研究中心监查工作。 对所负责的研究中心进行方案和研究相关的培训，与研究中心进行定期沟通以管理项目进行中的要求和问题。 评估研究中心工作的质量和完整性，确定研究中心是否是按照方案和适用的法规进行研究。将质量问题汇报给负责的PM和/或直线经理。通过追踪注册申报和批复、招募和入选、病例报告表（CRF）完成和递交、以及数据疑问产生和解决的情况，管理所负责研究中心的进展。 创建和维护与研究中心管理、监查访视的发现以及行动计划相关的文件，递交访视报告和其他所需研究文件。 负责相应研究中心的研究财务管理。 · 与其他职能部门共同合作。 · 完成直线经理和/或项目经理（PM）分配的其他工作。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.

We are seeking highly experienced Statistical Programmers (10+ years) with strong expertise in ADaM and TFL programming. Experience in Oncology/Immunology efficacy ADaMs—including ADTTE datasets for PFS, OS, DOR, BOR, ORR—is essential. Proficiency in KM plots, waterfall plots, and forest plots is required. Candidates must also have minimum 2 years of lead experience and 1 year of hands-on R programming. Experience in Phase 2 and Phase 3 studies is preferred.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.

Required skills and experience:• 2/3+ years of experience working with Azure and/or AWS or any other major cloud platform technologies• Provisioning, operating, and maintaining systems running on Azure and AWS cloud platforms including deployment/teardown and automation• Proficient with cloud platforms including IaaS & PaaS components, for example: Azure Virtual Machines/EC2 Instances, Golden Image/AMI management, Storage Accounts/S3 buckets, Network Security Groups/Security Groups, vNets/VPCs, Azure App Services, AWS Lambda, Kubernetes etc• Infrastructure as code (IaC), and CI/CD pipeline experience is required – example: Terraform, Bicep/ARM, CloudFormation, Gitlab, ADO• Hands-on scripting and automation experience (e.g., PowerShell, Python, Bash, Azure CLI, AWS CLI)• Proficient understanding of Windows and Linux operating systems from an administration perspective including OS configuration, patching, performance tuning, user/group management, system services, and troubleshooting• Knowledge of network (LAN, WAN, VPN) and web related protocols (e.g. TCP/IP, UDP, IPSEC, HTTP, HTTPS, routing protocols)• Management of monitoring and metrics using Azure Monitor, Log Analytics, Application Insights, CloudWatch and shared dashboards• Configuration and operation of backup solutions to protect and recover workloads (Azure Backup, AWS Backup)• Update Management (patching) experience on cloud based systems is required including remediation of patching issues• Experience with security policies, RBAC models, IAM roles and access provisioning, Security Groups• Good awareness of the latest features/capabilities of Azure and AWS platforms are desirable• Knowledge on installation, configuration, usage of CLI tools to manage cloud components is desirable• Experience with creation and maintenance of operations documentation for day to day issues and knowledge transfer• Excellent troubleshooting skills for Azure/AWS platforms including OS-level issues• Experience with ITIL/ITSM service operations processes including incident/request management, change and configuration management. Ideally ITIL Foundation certified. ServiceNow exposure is a bonus• Good to have: Understanding of AI-driven operations (e.g., AIOps, AI-assisted troubleshooting, log analytics insights)• Prior experience in Life Sciences area is also a bonus. Other highly regulated industry experience will be considered alsoEducation/certification:•    Degree level educated, preferably in science, maths or engineering areas.•    Azure Certification is a must - preferably Azure Administrator or Solutions Architect certified. AWS Associate level certification is preferred. 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 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 research Keep growing with an organization that encourages and invests in continuous professional and personal development Apply your business and leadership skills in an entrepreneurial and multi-disciplinary team Continue challenging yourself by addressing the toughest client issues, working across multiple geographies and solutions in a dynamic and crucial field for the industry Make a difference to patients by enabling the successful approval or launch of new treatments with features that are truly patient-centric Responsibilities 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.

Location: Athens (Greece) - Hybrid Contract: Full-time Language requirement: CV in English Join Us on Our Journey to Reimagine Healthcare IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services for the life sciences industry. With 85,000 employees across more than 100 countries, we create intelligent connections across the healthcare ecosystem through data, transformative technology, and deep industry expertise. We are now looking for a Pharmacovigilance Specialist to join our Greek organization. Role Overview The role is responsible for ensuring full compliance with pharmacovigilance (PhV) and product quality processes, acting as a key interface between operations, pharmaceutical clients and internal stakeholders (i.e. Quality). The position combines operational case handling, oversight, training, and continuous quality improvement. Key Responsibilities: Pharmacovigilance Operations Collect, assess, and process Adverse Events (AEs), Serious Adverse Events (SAEs), and Product Quality Complaints (PQCs)Perform case intake, triage, data entry, and follow-up activities while ensuring timely, accurate reporting to Pharma clientsPerform Source Data Verification (SDV), reconciliations and quality checksCompliance, Communication & Support Act as main point of contact for pharmacovigilance and product complaint teamsEnsure adherence to EU GVP guidelines, local regulations, and internal SOPsTraining & Capability Development Deliver PhV training programs across internal teamsLead onboarding and induction training for new hiresDesign and distribute monthly awareness initiativesMonitor training effectiveness and ensure full training compliance (maintain training records and documentation via DocuSign)Required Qualifications Bachelor’s degree in Life Sciences, Pharmacy, or related fieldMaster’s degree or certification in the Pharmacovigilance field is considered a plus2+ years of experience in Pharmacovigilance / Drug Safety with strong knowledge of GVP guidelines and AE/SAE/PQC reporting processesFluent in English and GreekStrong attention to detail and compliance mindsetStrong sense of ownership and accountabilityProven ability in training delivery and coordinationWhy Join IQVIA? At IQVIA, you can shape your career and choose the path that best supports your growth. With exposure to diverse geographies, capabilities, and therapeutic areas, you’ll find endless opportunities to learn, evolve, and make an impact. We believe that meaningful results come from the right people working in the right environment. Here, you’ll help clients drive healthcare forward and ultimately improve human health outcomes. It’s an exciting time to join us — and to reimagine what’s possible in healthcare. Moving healthcare forward. Together. IQVIA is committed to fostering a diverse and inclusive workplace. We believe that embracing diversity strengthens our teams, enhances innovation, and enables every employee to reach their full potential. 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.

Over IQVIA Nederland Bij IQVIA zitten we midden in een belangrijke transformatie: van dataleverancier naar strategische partner in de gezondheidszorg. Samen met onze klanten ontwikkelen we end-to-end oplossingen die écht impact maken. Dat doen we door onze expertise in healthcare, data, technologie en AI slim te combineren. Ons Nederlandse salesteam speelt een sleutelrol in deze ontwikkeling. We werken klantgericht, denken in oplossingen en zetten in op duurzame samenwerking in plaats van losse productverkoop. Jouw rol: Key Account Manager Als Key Account Manager ben je verantwoordelijk voor het uitbouwen van onze belangrijkste farmaceutische accounts en het creëren van nieuwe groeikansen. Je werkt nauw samen met de commercieel directeur en speelt een actieve rol in het realiseren van onze go-to-market strategie. Wat ga je doen? Ontwikkelen van nieuwe business en versterken van bestaande klantrelatiesOp strategisch niveau sparren met farmaceutische klantenSturen van commerciële en strategische initiatievenIdentificeren en benutten van samenwerkingen (o.a. met UMC’s)Vertalen van klantbehoeften naar slimme, geïntegreerde oplossingenSamenwerken met interne teams om complexe klantvraagstukken op te lossenActief bijdragen aan de positionering van IQVIA in de marktWat breng jij mee? 3–5 jaar saleservaring (in de farmaceutische sector is een pre)Goed inzicht in het Nederlandse zorglandschapErvaring met solution selling en complexe salestrajectenSterke communicatieve vaardigheden (NL & EN)Relatiebouwer op senior niveauProactief, ondernemend en resultaatgerichtMasterdiploma of gelijkwaardigWat bieden wij? Bij IQVIA werk je aan oplossingen die de gezondheidszorg verbeteren en patiënten écht vooruithelpen. Je krijgt de ruimte om te groeien, impact te maken en continu te blijven leren. Bouw mee aan de toekomst van healthcare — en maak het verschil. 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.

Natuurlijke producten | Fytotherapie | Direct sales apotheken Voor onze klant, actief in de ontwikkeling en distributie van natuurlijke gezondheidsproducten en fytotherapie, zijn wij op zoek naar een Farmaceutisch Vertegenwoordiger voor de regio West-Vlaanderen. Jouw verantwoordelijkheden Je bent verantwoordelijk voor de actieve promotie en verkoop van het productgamma in apothekenJe bouwt duurzame relaties op met apothekers en apotheekteamsJe geeft producttrainingen en adviseert over het gebruik van natuurlijke oplossingenJe zorgt voor een optimale visibiliteit en rotatie van de producten in het verkooppuntJe volgt jouw regio autonoom op en identificeert nieuwe opportuniteitenJouw profiel Eerste ervaring in farmaceutische of OTC sales is een sterke troefInteresse in of affiniteit met natuurlijke producten / fytotherapieCommercieel, proactief en resultaatgerichtSterke communicatieve vaardighedenGoede kennis van het Nederlands (kennis van Frans is een plus)Woonachtig in West-VlaanderenAanbod Uitdagende commerciële functie binnen een groeiend en mensgericht bedrijfProductgamma met duidelijke positionering in natuurlijke gezondheidAantrekkelijk salarispakket aangevuld met extralegale voordelenAutonomie en ruimte voor initiatiefIQVIA 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 Title: Expert Detailing RepresentativeLocation: ZambiaIndustry: Pharmaceutical / HealthcareEmployment Type: Contracted with IQVIA Overview:A leading global Consumer Healthcare company is seeking a dynamic and experienced Pharmaceutical Sales Representative to join their team as an Expert Detailing Representative (EDR) in Zambia. This role is ideal for a science-driven sales professional with a strong understanding of healthcare provider (HCP) engagement and a passion for promoting therapeutic solutions that make a difference. Key Responsibilities:As an EDR, you will be responsible for driving HCP awareness, advocacy, and recommendation of key consumer healthcare brands. You will: Conduct expert detailing sessions with HCPs, presenting clinical data and therapeutic benefits.Recruit HCPs to digital platforms and support digital engagement initiatives.Utilize multiple channels (face-to-face, remote, email, webinars) to drive meaningful engagement.Guide HCPs in accessing patient communication tools and digital resources.Encourage participation in Continuous Medical Education (CME) modules.Ensure consistent in-call quality and monitor expert performance metrics.Build and maintain strong relationships with HCPs in your territory.Distribute medical samples to support patient trials and product conversion.Track and achieve KPIs such as AWR, BRMO, and SoR.Meet or exceed territory sales targets.Provide market insights and competitor intelligence to internal teams.Organize and support educational events and meetings.Uphold compliance standards and represent the field team professionally.Qualifications & Requirements: Education: BSc or equivalent in a relevant scientific field.Experience: Minimum 5 years in pharmaceutical sales or a related healthcare role.Skills:Strong communication and presentation abilities.Proficiency in digital tools and CRM systems (e.g., Veeva).Analytical mindset with the ability to interpret sales data and KPIs.Excellent time management and organizational skills.Knowledge of pharmaceutical compliance and ethical standards.Other Requirements:Valid driver’s license and access to a reliable vehicle.Why Join Us?This is an exciting opportunity to be part of a forward-thinking team that values innovation, professional development, and impactful healthcare solutions. You’ll play a key role in shaping HCP engagement and driving brand success in a dynamic market. #LI-DNP #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.

IQVIA is hiring Clinical Research Associates! Join IQVIA today and make an impact on patients’ outcome! Job OverviewPerform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Responsibilities Performing site selection, initiation, monitoring and close-out visits, plus maintaining appropriate documentationSupporting the development of a subject recruitment planEstablishing regular lines of communication plus administering protocol and related study training to assigned sitesEvaluating the quality and integrity of site practices – escalating quality issues as appropriateManaging progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution Qualifications Minimum of a Bachelors Degree in scientific discipline or health care.  Experience of 1 year in on-site monitoring clinical trials. Good knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines). Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable). Written and verbal communication skills including good command of Polish and English language. Ability to establish and maintain effective working relationships with co-workers, managers, and clients. Connect to great opportunity™ ​IQVIA™ is a strong advocate of diversity and inclusion in the workplace.  We believe that a work environment that embraces diversity will give us a competitive advantage in the global marketplace and enhance our success.  We believe that an inclusive and respectful workplace culture fosters a sense of belonging among our employees, builds a stronger team, and allows individual employees the opportunity to maximize their personal potential. #weareIQVIA #projectpatientfocus #LI-Remote #CRASDAJD #CRA #fspcares 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 119.400,00 zł - 280.000,00 zł. 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.

Role Overview We are looking for a Product Owner who sits at the intersection of business, customer, and technology. You will own the vision and roadmap for our authentication and identity products, translate strategy into deliverable work for the engineering team, and keep us ahead of the curve on identity standards and the evolving threat and user-experience landscape. This is a hybrid profile: you think like a product marketer (market, positioning, customer needs) while carrying genuine technical depth, enough to engage credibly with engineers and security teams on protocols and emerging authentication approaches. Essential Functions Maintains the product vision and roadmap and supports growth opportunitiesSupports the product strategy by staying up to date on market trends and understanding the latest customer needsMonitors and adheres to success metrics, analyzes data for insights, and coordinates with partner teams to support business strategiesTranslates product roadmap features into product requirements, including features, user stories, and acceptance test criteriaPrioritizes and breaks down high-level requirements into detailed user stories that the development team can execute againstActs as the product expert for users, bringing creative, ad-hoc solutions to real use casesMonitors and evaluates product progress, including outcomes of deliverables, and recommends improvements based on internal and customer feedbackHelps mitigate impediments to ensure successful completion of release/sprint goalsDomain-Specific Responsibilities (Authentication & Identity) Runs structured technology watch on the authentication and identity space (OpenID Connect, passkeys, verifiable credentials, and related standards) as they evolveTranslates standards and ecosystem changes into clear product implications and communicates them to engineering, security, and leadershipBalances three competing forces in every authentication decision: user experience (friction), security posture, and compliance/regulatory constraintsPartners with marketing to articulate the value and differentiation of identity features to both technical and non-technical audiencesQualifications Required Bachelor's degree in Computer Science, a related field, or equivalent experienceDemonstrated product ownership experience (roadmap, backlog, user stories, working with agile development teams)Working knowledge of authentication and identity concepts (OpenID Connect, OAuth, or SAML)Comfort working with data and success metrics to inform prioritizationStrongly Preferred Prior product experience in identity, security, API, or developer-facing productsAbility to conduct independent technology watch and form a defensible point of view on emerging standards (e.g., passkeys/WebAuthn)Exposure to product marketing or go-to-market workNice to Have Familiarity with relevant compliance and regulatory frameworks affecting identity (e.g., GDPR, eIDAS, sector-specific requirements)Experience communicating technical concepts to commercial and executive stakeholdersIQVIA 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 160 200,00 zł - 297 300,00 zł. 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.

Our MedTech Field Service Technician experiences a unique opportunity employ their technical experience by collaborating with healthcare professionals and leading technical initiatives in medical device technology.  You will be responsible for troubleshooting, repairing, and updating medical devices inside of hospitals, pharmacies and other clinical settings. The current product line being supported is an automated medication dispensing system.   This is an ON-CALL, Field Service Technician opportunity with approximately 20-25 hours per week.  While the hours are estimated and need is not guaranteed, this is historically the need. What you will be doing in the role: Troubleshoot and repair existing devices and document the activities performed.  Replace hardware parts, as well as software updates and calibrations.   Perform bi-annual or yearly preventative maintenance as determined by the customer.  Assist in the installation and implementation of new devices at customer locations.  Conduct routine system checks and record data from product tests after installation and configuration.   Maintain and stock parts and tools assigned by customer.  Be available on-call including nights and weekends. Training for this role will be provided and is paid Job Requirements:   Must have intermediate troubleshooting abilities in the disciplines of electronics, mechanics, and electromechanical systems.  Experience as a military technician, computer technician or other complex electronics technician preferred. Experience supporting automation equipment in a healthcare setting is a plus.    Experience in healthcare, field service, engineering, biomedical, maintenance, customer service, pharmacy technician, electronics, electrical, technical work, or IT is beneficial for this position.   Strong communication skills and ability to provide exceptional customer support.  This position requires a considerable amount of pushing, pulling, stooping, bending, and lifting to 70 LBS  Ability to clear hospital vendor credentialing requirements, including proof of vaccination status, required  Travel Requirement: Travel locally for up to 2-3 hours to support customer needs.  Respond to and arrive at customer sites within the service ticket’s Service Level Agreement (within 4 hours, 8 hours, 12 hours, or 24 hours per the details of each ticket)   Must have an active driver license and a personal vehicle to use for job related assignments Travel, and your time traveling is paid, as is mileage. Preferred Attributes: A+ certification preferred Ability to work independently in customer settings with minimal supervision. IQVIA MedTech CFS takes the approach to helping customers drive healthcare forward in this challenging and fast-paced environment. We help customers accelerate results, improve patient outcomes, and unleash new opportunities. Benefits: This position is not eligible for our Medical Benefits. Vaccine/Immunization/Hospital Credentialing Requirement: A required function of this job requires individuals to enter various healthcare facilities.  Thus, upon selection, individuals must complete healthcare facility credentialing process.  To obtain credentials, individuals must meet the immunization requirements specified by the facility.  Individuals are typically required to have completed/up to date: Measles, Mumps & Rubella vaccine, Varicella (chicken pox) vaccine, Negative Tuberculosis (TB) Test, Tetanus, Diphtheria & Pertussis (Tdap) vaccine, Hepatitis B vaccine, Influenza vaccine (seasonal), and COVID-19 vaccine primary series (heavily enforced by most facilities, some require booster(s)). Please note, IQVIA complies with all applicable laws regarding reasonable accommodations or exemptions for religious, medical, or other legally protected reasons, however, our client’s requirements may supersede this.  *Please note: Due to the nature of this role, it is not eligible for Visa sponsorship. #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 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 $31 - $35 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.

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 (corrective & preventive action) 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• 6-9 years’ relevant experience and/or equivalent combination of education, training and experience. 3-5 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 OverviewManaging assigned monitoring responsibilities (simple protocols/ non-protocol tasks) competently, in a timely manner and with quality. Essential Functions• Under minimal supervision perform centralized monitoring activities for the assigned projects which includes but is not limited to•      On time completion of assigned role specific trainings (self-learning courses, instructor led training, acknowledgement of e-SOP/WI etc.) and related assessment Loading and updating the active databases with details of participating sites•      Provisioning of access for Infosario Portal.•      Ensuring on-time completion of documentation(s) that form a part of the regulatory dossier for kit shipment [Kit Contents Chart(KCC)/Packing List//Import Permit].•      Monitoring on-time release of patient laboratory report by following up on the associated pending activity(ies) with related team(s).•      Ensuring that documentation is available for all monitoring activities performed for real-time audit readiness•      Participation in department/process improvement initiatives as applicable. Qualifications• High School Diploma or equivalent  Req• Fresher/Intern only preferred• Requires basic job knowledge of systems and procedures obtained through prior work experience or education.• Must be able to comply with all applicable standards as required by the company.• Demonstrated ability to handle multiple tasks.• Demonstrated ability of critical thinking and problem solving.• Strong written and verbal communication skills including good command of English language.• Strong interpersonal, communication, organizational, and time management skills.• Computer proficiency in word processing and spreadsheet applications.• Demonstrated ability to work in a fast-paced, high stress environment highly desirable.• Ability to establish and maintain effective working relationships with coworkers and managers. 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 OverviewManage a team of clinical staff working in support of clinical studies to ensure projects are appropriately resourced and employees are trained and meeting project objectives.Essential Functions• Manage staff in accordance with organization’s policies and applicable regulations. Responsibilities include planning, assigning, and directing work, assessing performance and guiding professional development, rewarding and disciplining employees, and addressing employee relations issues and resolving problems.• Participate in the selection for hiring new employees by conducting candidate review and participating in the interviewing process. Ensure that new employees are properly onboarded and trained.• Ensure that staff has the proper materials, systems access and training to complete job responsibilities. Provide oversight for the execution of the training plan, SOP review and training experiences, as applicable.• Participate in the allocation of resources to clinical research projects by assigning staff to clinical studies based on their experience and training.• Manage the quality of assigned staff's clinical work through regular review and evaluation of work product.• Identifies quality risks and issues and create appropriate corrective action plans to prevent or correct deficiencies in performance of staff.• Ensures that staff are meeting defined workload and quality metrics through regular review and reporting of findings as outlined by clinical operations management.• May collaborate with other clinical teams and other functional leadership to manage project related challenges and to achieve exemplary customer service.• Participates in corporate or organizational departmental quality or process improvement initiatives.Qualifications• Bachelor's Degree Degree in scientific discipline or health care preferred. Pref• Prior clinical trial experience including experience in a management/leadership capacity or equivalent combination of education, training and experience.• In-depth knowledge of applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines).• Good leadership skills.• Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint.• Written and verbal communication skills including good command of English.• Excellent organizational and problem solving skills.• Effective time management skills and ability to manage competing priorities.• 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.

Position Summary The SEAT (Southeast Asia and Taiwan) Rare Diseases Lead directly reports to Senior Director, Rare Diseases EU & Int'l, Global Rare Diseases Business Unit. The function leads the full spectrum of activities dedicated to the Rare Diseases product portfolio and coordinates the implementation and execution of strategies and projects derived from the company international brand plans to achieve the Country full potential. In addition, the SEA Rare Diseases Lead holds responsibility for local sales performance and ensuring that partners implement the appropriate strategies and actions necessary to achieve commercial objectives. This role is pivotal in driving alignment and execution across all stakeholders to meet business goals effectively. The role also requires the individual to spend a significant portion of their time working alongside partners in the field, ensuring close collaboration and effective support across the territory. Key Tasks and Responsibilities Develop and execute Customer brand plans. Liaise with Portfolio Brand and Medical Manager and other functionsIdentify, prioritize and execute critical commercialization activities for product portfolioDirect sales responsibility & country BU managementIncrease and optimize strategic level of the RD unitAlign brand strategies and convert them into local market and reimbursement settingsOrganize and run added value programs to guide the company through challenging RD market environmentGather and assess data on disease areas, indications, key customers and business environment (i.e. search and critically evaluate clinical literature, business sources and market research on incidence/prevalence, product profile, competitive therapies/ companies, key customers and related business issues)Help develop and support critical assumptions used to quantify the market and potential value of present and (potential) new products under multiple scenarios, including all country BU operating expense budgetsCoordinate efforts in team environment and with other departments (Mkt Access, PV&QA, BK, local CS, supply, finance, HR, legal, regulatory, advocacy, etc.)Develop in-depth understanding of the RD products related markets, therapeutic areas and dynamics as well as critical success factorsEnsure, through direct involvement, the development and implementation of the sales plans to achieve sales targets Effectively lead the planning, organization, leadership and control of the business unit through the appropriate processes and in accordance with the client philosophy, values and ethical codeRequirements and Qualifications Qualifications will include a minimum of University level educationLife science, medical background a plusMinimum 5+ years commercial experience/Market Access in rare diseases is requiredStrong marketing and sales experience in RD field. In alternative a previous marketing role with extensive external activities and KOL contacts Holistic understanding of the APAC pharmaceutical ecosystems. Knowledge of local pricing and reimbursementExperience in RD product launch Strong market knowledgeSolid financial acumenProven People Management ExperiencePersonality criteria The successful candidate will be a self-reliant, self-motivated entrepreneur with a demonstrated ability to build businesses as well as enduring, authentic and productive internal collaborations.Team player and able to work with several disciplines in a multicultural environmentStress resilientProblem solving: leads others to solve complex problems and takes a broad perspective to identify innovative solutions.High flexibility and ability to work in a matrix organizationAbility to manage complexity and build trustGood analytical and tactical skillsFluent in English and MandarinIQVIA 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 OverviewAssociate Clinical Leads are an integral part of clinical trial delivery, working alongside clinical teams to improve patients’ lives by bringing new drugs to the market faster. The Associate Clinical Lead is a member of the core project team responsible for clinical delivery of clinical studies to meet contractual requirements in accordance with Standard Operating Procedures (SOPs), policies and practices. Associate Clinical Leads partner with Project Leaders and other functional teams to secure delivery requirements are met at all times. Essential Functions• Ensure clinical delivery of assigned projects in compliance with regulatory requirements (International Conference on Harmonization (ICH)-Good Clinical Practice (GCP), protocol), customer requirements (contract), and internal requirements (policies, Standard Operating Procedures (SOPs), project plans).• Accountable for meeting projects’ recruitment targets and ensuring appropriate recruitment strategies are in place.• Contribute to the development of the project risk mitigation plan and manage clinical risks throughout the project’s lifecycle.• Ensure clinical quality delivery by identifying quality standards/requirements, planning how compliance will be measured, monitoring and overseeing management of clinical quality issues.• Manage clinical aspects of Project Finances including Estimate at Completion (EAC). Understand the scope of clinical delivery and create plans to deliver. Monitor and manage changes against baseline Estimate at Completion (EAC) and identify additional service opportunities or out of scope work.• Identify clinical stakeholder landscape for the project and manage both internal and external stakeholders through effective communication and resolution management.• Collaborate with the clinical team to support milestone achievements. Report to internal and external stakeholders as per project scope requirements.• Resourcing and Talent Planning of the clinical team. Manage the clinical team at project level to successfully deliver the project through the establishment of high-quality operational plans and guidance and project related trainings.• Conduct regular team meetings and communicate appropriately to achieve objectives.• Support professional development by providing feedback to clinical team line managers on performance relative to project tasks.•  May work as the sole Clinical Lead on projects with 1-2 service lines and single/few countries or alongside more senior Clinical Leads to deliver large, global trials.;• May attend site visits as applicable in support of project delivery. Qualifications• Bachelor's Degree Bachelor's Degree in health care or other scientific discipline required• Requires 3 years clinical research/monitoring experience or equivalent combination of education, training and experience.;• Requires good knowledge of applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.;• Requires broad protocol knowledge and therapeutic knowledge.;• Requires good understanding of Clinical Research industry (drug/device/technology/etc.) and the relevant environments in which it operates.• Requires basic understanding of project finances.;• Knowledge of clinical trials - Knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements i.e., International Conference on Harmonization (ICH) and Good Clinical Practice (GCP) and relevant local laws, regulations and guidelines, towards clinical trial conduct.;• Communication - Strong written and verbal communication skills including good command of English language.• Problem solving - Problem solving skills.• Organization - Planning, time management and prioritization skills.• Prioritization - Ability to handle conflicting priorities.• Quality - Attention to detail and accuracy in work.• Results-oriented approach to work delivery and output.; and PowerPoint.;• IT skills - Good software and computer skills, including Microsoft Office applications including but not limited to Microsoft Word, Excel and PowerPoint.;• Collaboration - Ability to establish and maintain effective working relationships with coworkers, managers and clients.• Cross-collaboration - Ability to work across cultures and geographies with a high awareness and understanding of cultural differences.• Effective communication - Ability to influence without authority.• IQVIA Core Competencies - Ability to demonstrate all IQVIA competencies (Client Focus, Collaboration, Communication, innovation, Ownership). 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 OverviewProvides first level support on workstations or for applications.Essential Functions• Processes and provides first level support for technical assistance and resources from internal and/or external customers.• Communicates with end users to clarify and define requirements.• Resolves various routine problems and escalates the more complex issues to the appropriate support area for resolution.• Maintains call information in database using commercial software.• May work with monthly charge back reports.• May schedule configuration and installation of PC workstation hardware and software.Qualifications• Associate's Degree Computer Science or equivalent, or equivalent technical training Req• One (1) years related experience or training Req Or• Equivalent combination of education and experience Req• Familiarity with mainframe, distributed, PC, LAN, or telecommunications equipment and related components in order to understand client's technical needs, or may have experience in customer service role.• Ability to carry out some analysis and information gathering to resolve problems on routine matters.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.