IQVIA

Opening StatementIQVIA is creating a dedicated Governance Team to provide single operational ownership for data platform services, covering access management, incident and request handling, monitoring, maintenance, governance, improvements, automation and reporting. As a Manager, Data Platforms SRE, you will build and lead this team in India and establish a scalable, measurable operating model aligned to ITIL and managed service principles. This role addresses critical structural inefficiencies where senior engineering talent is heavily involved in operational control and governance-driven activities, reducing time available for high-value engineering and platform innovation. The Governance Team will establish a clear separation between operational ownership and platform engineering, enabling the organization to treat platform operations as a managed service with defined KPIs, SLA/SLO tracking, and continuous improvement. You will partner closely with Platform Engineering for L3 and engineering decisions while owning day-to-day service delivery for Databricks and Snowflake operations.Job OverviewYou will own the day-to-day service delivery for Data Platforms operations (Databricks and Snowflake) and governance activities, while partnering with Platform Engineering for L3 and engineering decisions. This management role requires building the operational foundation for IQVIA's data platform services, moving from a reactive, ad-hoc support model to a predictable, scalable operating model based on ITIL standards. Your leadership will establish the operational gatekeeper function that tracks policy adherence, compliance gaps, and recurring operational risks across the data platform landscape. Success in this role means establishing measurable service KPIs, reporting artifacts tracking volumes and MTTR trends, and driving continuous improvement from reactive support toward managed service delivery with defined SLA/SLO verification. 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 OverviewAs a Senior Data Platforms SRE, you will serve as a technical escalation point and resolve higher complexity incidents and technical problems end to end. This role requires advanced troubleshooting expertise in data platforms, operational discipline, and the ability to drive service improvements across the governance team. You will work directly with Databricks and Snowflake platforms deployed on Azure and AWS, investigating non-trivial technical issues, implementing platform guardrails, and mentoring junior engineers to elevate the team's operational maturity. The position combines hands-on technical work with service improvement initiatives, including defining operational metrics, tracking incident resolution trends, and contributing to SLA/SLO verification to ensure platform reliability and cost effectiveness. Level 2 support engineers handle technically complicated issues that exceed the competence of Level 1 support, focusing on incident resolution through deep technical knowledge and advanced troubleshooting skill.Key ResponsibilitiesAdvanced Incident Handling & Escalation: Investigate non-trivial job and pipeline failures, performance and capacity symptoms, and recurring platform issues. Coordinate escalation to platform engineering or vendors with complete diagnostics, including root cause analysis, system logs, and performance metrics to ensure rapid resolution. L2 engineers perform deep diagnoses to trace and resolve issues, managing support tickets to ensure timely resolution of all technical incidents .Resource & Cost Governance: Perform spend anomaly checks to identify runaway queries, oversized clusters, and job loops that drive uncontrolled costs. Drive remediation actions including shutdowns and guardrails using policy and operational authority, ensuring alignment with financial controls and budget targets.Platform Guardrails Implementation: Implement and maintain cluster policies and operational restrictions that prevent uncontrolled cost growth, aligned with governance objectives. Configure and enforce workspace-level controls, quota management, and resource limits across Databricks and Snowflake environments.Environment Lifecycle Execution: Support workspace and environment provisioning and decommissioning activities, including Infrastructure as Code driven provisioning where defined. Execute environment setup, configuration validation, and teardown procedures following established operational standards.Service Improvement & Metrics: Help define and track operational metrics including incident volumes, resolution trends, and mean time to resolution. Contribute to SLA/SLO verification and improve documentation quality and consistency across the service to support continuous operational improvement. L2 support engineers maintain detailed documentation and knowledge articles as key activities in their role.Mentoring & Coaching: Mentor junior engineers on troubleshooting methodologies, ticket handling best practices, and technical documentation standards. Review tickets for completeness, ensure clean handoffs between support tiers, and raise the overall operational maturity of the team through knowledge sharing and skills development. 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 OverviewAs a Data Platforms SRE, you will execute operational tasks and resolve issues using runbooks and escalation paths. This role is critical to maintaining the stability and performance of IQVIA's enterprise data platforms, which require engineering expertise for efficient management. You will work within the Governance Team's operational framework to ensure platforms remain secure, audit-ready, and cost-optimized by default. Your responsibilities encompass four key operational areas that directly support platform health and user productivity.Key ResponsibilitiesIdentity and Access Management: Process onboarding and offboarding tickets, add or remove users and accounts, reset credentials and permissions, and execute access requests for specific catalogs, schemas, tables, or external locations in line with defined controls .Technical Support: Triage incidents, check logs for errors, provide first responses to user requests, and escalate when needed with clear evidence including logs, timestamps, and reproduction steps.Monitoring and Housekeeping: Perform daily and weekly checks of platform dashboards to catch runaway queries, oversized clusters, or job loop errors before they generate excessive costs. Track basic cost and usage signals, and help clean up idle or unused resources following established guidance. Governance Implementation: Support the implementation and improvement of the Governance framework and policies, build script and automation, policies control and provisioning within the Data Platforms, supporting FinOps and best practices implementation. Documentation: Update operational documentation and ensure ticket notes are professional, specific, and customer-visible as required by support guidelines. Maintain knowledge base articles and troubleshooting guides to meet objectives for customer request fulfillment and issue resolution. 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.

Tools & Methodologies: Having knowledge on these is a must.- HPQC- SQL- Agile- IterativeRoles & Responsibilities- Authoring test cases- Creation of test data to support test case execution and supports creation and maintenance of libraries of reusable test data sets- Executes test cases and logs/retests issues found- Reviewing requirements specifications for testability and verifying traceability of testing to requirements and vice-versa- Reports status, progress and concerns in a proactive, consistent and accurate manner to IT Project Manager.- Knowledge and understanding of system and project testing strategies/approaches and the CSV (Computer System Validation) and SLC (Software Life Cycle) processes adopted by Quintiles- Keeps current on software applications testing industry knowledge and acquiring industry computer validation systems knowledge by attending industry conferences, reading industry periodicals and training via workshop attendance and self-study.- Performs other duties as required- Exposure to SQL queries authoring at basic level and understanding of Database concepts.- Assists in internal peer reviews of test cases from other Analysts prior to and following execution as required to ensure issues/errors with the test scripts are identified and resolved- Possess a working understanding of the requirements elicitation, analysis, and specification process including user requirement specifications and functional specifications.- Knowledge of Healthcare industry standards is desirable especially CFR Part 21, GCP, Electronic Data Capture.  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 Principal Biostatistician will serve as the statistical lead for clinical studies, providing scientific oversight, strategic guidance, and hands‑on statistical support across late‑phase clinical trials. This role requires a highly experienced biostatistician capable of working independently, representing the Biostatistics function within cross‑functional teams, and delivering high‑quality statistical input throughout study design, execution, and analysis. Key ResponsibilitiesStatistical Leadership & Study SupportServe as the primary statistical lead and main point of contact on the Clinical Trial Team (CTT), representing Biostatistics with confidence and professionalism.Work independently to support clinical teams, providing proactive statistical guidance throughout the study lifecycle.Lead statistical strategy discussions, including endpoint definitions, analysis methods, risk mitigation, and regulatory expectations.Statistical Analysis & MethodologyIndependently author Statistical Analysis Plans (SAPs), including drafting in collaboration with cross‑functional partners, pharma statisticians, or from finalized protocols.Implement non‑standard or advanced statistical methodologies, such as:Complex time‑to‑event analysesMMRM and other longitudinal modelsMethods aligned with estimands, including deep understanding of competing policies, assumptions, and analytical implicationsPerform or oversee statistical analyses, ensuring scientific rigor and regulatory compliance.Conduct sample size calculations using SAS or R, and justify design assumptions when engaging with clinical leadership.Programming CollaborationWork closely with statistical programmers, providing clear direction, reviewing outputs, and ensuring alignment between the SAP and programming deliverables.Contribute hands‑on with SAS programming, including working with clinical datasets and performing analyses when needed.Experience with R, CRM systems, or advanced tools is considered an asset.Cross‑Functional EngagementActively participate in CTT meetings, offering statistical expertise and driving alignment across clinical, programming, data management, and medical writing partners.Proactively communicate with team members to anticipate needs, address issues, and ensure clarity on statistical approaches.Provide clear, influential explanations of statistical concepts to non‑statistical stakeholders.Qualifications & ExperienceAdvanced degree in Biostatistics, Statistics, or a related field (PhD preferred; Master’s accepted with significant experience).Proven experience working independently as a study statistician in late-phase (Phase II/III) clinical trials.Experience in pharmaceutical industry strongly preferred; CRO experience is a plus.Hands‑on expertise with clinical outcomes studies, including cardiovascular events, symptomatic endpoints, and quality‑of‑life measures.Demonstrated ability to implement complex statistical methods and guide cross‑functional teams through analytical decision‑making.Proficiency in SAS; working knowledge of R is advantageous.Experience with regulatory submissions and interaction with health authorities is a plus.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.

This opportunity is available in multiple locations across Europe (within the European Union, Switzerland and the UK). Please don’t hesitate to apply even if you don’t see your preferred location listed. The role can be hybrid or fully home‑based. Please submit your CV in English. 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 Global Scientific Lead for Clinical Outcome Assessment (COA) Endpoint Strategy serves as the senior scientific authority in the COA Consulting team within Patient Centered Solutions. This role brings deep expertise in COA measurement science and Patient Experience Data (PED) more broadly, to differentiate client solutions through expert-driven, highly insightful endpoint and PED 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. The role provides organisational leadership for COA science through a combination of direct people management and influence by setting the standards and strategy for the scientific work of the consulting team. Key responsibilities include: People and organizational leadership Serve as the global scientific lead for consulting activities, providing strategic oversight and leadership across the PCS consulting organisation Lead and develop talent through a combination of direct line management, broader mentoring, and active cultivation of scientific capabilities across the consulting team Champion excellence in scientific outputs, driving consistency, quality, and innovation in clinical outcome assessment (COA) and PED–related deliverables Set and shape the long-term vision and strategy for scientific activities within consulting, working in close partnership with senior leadership Client Strategy Leadership & Scientific Differentiation Develop COA endpoint and PED strategies across clinical development programs, including primary and key secondary endpoint positioning in consulting projects. Bring senior COA and PED expertise into client meetings, workshops, and strategic discussions. Differentiate proposals and client solutions through expert-driven COA and PED 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 senior 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 and PED strategy and development work.  Review and approve key scientific deliverables to ensure quality, rigor, and alignment with best practices.  Mentor and coach COA and PED scientists and 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 and PED 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.  Strong experience supporting FDA-facing endpoint strategy and regulatory interactions.  Broad experience across PED methodologies and application of PED by regulators, payers and other stakeholders desirable Proven ability to lead, mentor, and oversee multidisciplinary scientific teams.  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.  Please submit your CV in English. 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.

Regulatory Affairs IVDR - Contractor (North Africa) Location: Algeria, Morocco, or Tunisia (Remote/Hybrid as applicable)Contract Type: Contractor About the Opportunity We are seeking an experienced Regulatory Affairs IVDR Contractor to support regulatory activities across the EMEA region, with a key focus on In Vitro Diagnostic Regulation (IVDR) transition projects, product registrations, regulatory compliance, and change control activities within the medical diagnostics industry. This is an exciting opportunity for a regulatory professional with experience in medical devices, ideally IVDs, who thrives in a fast-paced, cross-functional environment and is passionate about ensuring regulatory compliance while supporting business objectives. Key Responsibilities Support the development and execution of regulatory submission plans related to IVDR transition projects across the EU region.Collaborate with global Regulatory Affairs teams, Legal, Manufacturing, Supply Chain, Marketing, Commercial teams, and distributor markets to support regulatory initiatives.Manage and support applicable change control projects by coordinating with manufacturing sites and relevant stakeholders to obtain regulatory documentation and dossiers.Support product registrations and amendments to existing regulatory approvals and certificates.Maintain regulatory databases and proactively escalate risks where necessary.Track, monitor, and report submission status and regulatory milestones through defined KPIs and reporting platforms.Provide backup support for local Regulatory Affairs activities when required.Represent Regulatory Affairs at project meetings, including IVDR and change control forums.Monitor regulatory developments, legislation, and industry standards within supported markets.Conduct regulatory impact assessments and communicate relevant changes to internal stakeholders.Support strategic Quality and Regulatory Affairs objectives.Perform additional regulatory and compliance-related duties as required.Minimum Requirements Education & Experience Minimum of 2 years' experience in Regulatory Affairs within the Medical Devices industry, preferably in In Vitro Diagnostics (IVDs).Demonstrated knowledge of the medical diagnostics industry and regulatory environments within supported regions.Experience supporting regulatory submissions, registrations, and change management activities.Skills & Competencies Strong project management capabilities.Ability to work effectively within cross-functional and multicultural teams.Working knowledge of local Ministry of Health regulations, regulatory requirements, industry standards, and guidance documents.Excellent verbal and written communication skills in English.French language proficiency will be advantageous.Strong attention to detail and organizational skills.Excellent interpersonal and stakeholder management abilities.High levels of professionalism, integrity, and diplomacy.Ability to manage confidential information with discretion.Strong analytical and problem-solving skills.Preferred Candidate Location Applicants must currently be based in one of the following countries: AlgeriaMoroccoTunisiaWhat We're Looking For The successful candidate will be a proactive regulatory professional who can work independently, manage multiple priorities, and collaborate effectively with stakeholders across various functions and geographies. Interested candidates are invited to submit their CV highlighting their relevant Regulatory Affairs and IVDR experience. #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.

Amphastar Pharmaceuticals, Inc. BAQSIMI® Job Description As the only global provider of commercial solutions, IQVIA understands what it takes to deliver nationally and internationally. Our teams help biopharma, medical device and diagnostic companies get their therapies to the people who need them. We help customers gain insight, access to their markets, and demonstrate their product’s value to payers, physicians, and patients. A significant part of our business is acting as the company’s sales force to physicians or providing nurses to educate patients or prescribers. With the right experience, you can help deliver medical breakthroughs in the real world. IQVIA has the world’s largest Commercial Sales & Medical Solutions (CSMS) organization dedicated to the launch and marketing of pharmaceutical and medical products. With a focus on providing talent for field/inside sales, medical device support, clinical support, and medical affairs our CSMS division has 10,000+ field professionals in more than 30 countries addressing physician and patient needs. We are excited to announce that in partnership with Amphastar Pharmaceuticals, we are currently looking for a Pharmaceutical Sales Representative – Diabetes to join our team. In this position, you will promote products in the Endocrinology/Diabetes space. The Pharmaceutical Sales Representative - Diabetes is primarily responsible for achieving sales forecast and gaining adoption and utilization of the drug. This is accomplished by establishing mutually beneficial business relationships with targeted accounts and physicians key to the sales success of the promoted products. The sales representative is also responsible for coordinating sales strategies with appropriate teammates to maximize sales in assigned territory. RESPONSIBILITIES ·       Manage customer relationships in defined geographic territory to strengthen the company brand ·       Meet or exceed assigned sales volume objectives ·       Develop territory call plans ·       Coordinate appropriate support resources (i.e., Client Services, MD’s, etc.) to maximize and strengthen customer relationships ·       Manage selling processes to include the following areas: forecasting, client starts, product starts, productivity and client relations ·       Maintain sales prospect lists/sales funnels as required to achieve sales volume targets ·       Maintain a detailed customer database within Salesforce CRM (Customer Relationship Management) system ·       Design and implement Quarterly Business Plan for assigned geography ·       Attend Technical and sales training programs to further development competencies ·       Manage company expense within policy and defined budget ·       Provide timely feedback to management regarding market trends, competitor activity, and new product/services improvements ·       Demonstrate the highest level of integrity in all customer/company interactions; replace patient confidentiality as per HIPPA regulation ​ Required Qualifications: ·       4-year degree from an accredited college or university (Required) ·       Minimum 2 years of pharmaceutical sales experience with documented sales success (Preferred) ·       Endocrinology/Diabetes experience (Preferred) ·       Valid driver’s license and current auto insurance (Required) ·       Must be willing to travel up to 50% of the time (Required) ·       Exceptional verbal and written communication skills ·       Successful candidates will demonstrate the following competencies: Action Oriented, Drive for Results, Sales Persuasion, Dedication, Perseverance, Ingenuity, and Adaptability ·       Demonstrated ability to manage and develop an assigned territory with minimal supervision #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 85-90K annually. 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 OverviewDesigns/develops software solutions requiring general domain knowledge and developing business experience.Analyzes user requirements/needs and makes decisions within limited parameters under regular supervision. Essential Functions• Designs/develops software solutions requiring general domain knowledge and developing business experience.• Works at all layers of the application stack including front-end user interface and backend development.• Analyzes user requirements/needs and makes decisions within limited parameters under regular supervision.• Supports and may lead projects within own organization with limited complexity, including the development of small to medium size system components.• Has broad understanding of quality standards and work requires minimal revision.• Reviews functional specifications and other validation deliverables as assigned.• Provides peer support and helps on-board new Associate Software Engineers to the team.• Typically requires 5 years of prior relevant experience. Qualifications• Bachelor's Degree Computer Science, a related field, or equivalent experience Hands on expereince in develeping enterprise level web development, mobile appWell verse with UI technologies and framework like react, react native ,javascript, JQuery, node JS, Angular Good understanding of Cloud concepts Good understanding of DevOps basics, CI/CD and automation. 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.

Territory & Application Specialist Location: Ghana#LI-DNP #LI-DNI  #LI-CESIQVIA 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.

Field Service Engineer Location: Ghana#LI-DNP #LI-DNI  #LI-CESIQVIA 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.

Market Lead – Animal Health Location: Zimbabwe We are seeking an experienced and driven Market Lead to drive commercial growth and market development within the animal health sector across Zimbabwe and surrounding markets. This role is ideal for a commercially astute professional with strong marketing expertise, a passion for building partnerships, and the ability to execute impactful strategies in a dynamic, multi-country environment. Key Responsibilities Develop and execute go-to-market and marketing strategies to drive business growthLead annual marketing plans, campaigns, and product positioning initiativesConduct market research and competitive analysis to identify opportunitiesSupport and collaborate with sales teams and distributors to increase product adoptionBuild and manage strong relationships with key customers, distributors, and stakeholdersProvide training, tools, and marketing support to field teamsEnsure alignment with regulatory requirements and quality standardsMonitor sales performance, market share, and profitabilityCollaborate cross-functionally with Regulatory, Technical, and Finance teamsRequirements Bachelor’s degree in Marketing, Business, Animal Science, Veterinary Science or similarMinimum 5–7 years’ experience in marketing or commercial roles within the animal health industry (preferred)Proven experience in multi-country or regional market managementStrong understanding of animal health markets and regulatory environmentsExcellent communication, presentation, and stakeholder engagement skillsStrong analytical and strategic thinking abilityWillingness to travel frequently within Zimbabwe and the regionKey Competencies Strong customer focus and relationship-building skillsHigh levels of accountability and ownershipAbility to influence and communicate effectively across diverse audiencesAdaptable, resilient, and comfortable working across different cultures and marketsSelf-driven with a strong commercial and results-oriented mindsetWho Should Apply We are specifically looking for candidates with a background in Animal Health, who bring both commercial acumen and technical understanding of the industry. #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.

Voor een opportuniteit bij één van onze klanten zoekt IQVIA een farmaceutisch afgevaardigde. Je komt terecht bij een jong en dynamisch bedrijf met een uitstekende reputatie en een sterke groei. De organisatie is marktleider binnen haar domein en staat bekend om haar familiale en warme bedrijfscultuur, met weinig verloop en collega’s die al jarenlang met engagement meebouwen aan het succes. Wat houdt de job in? Bezoeken van zelfstandige apotheken en apotheekgroeperingen binnen jouw regioPromoten en positioneren van een sterk portfolio binnen de oftalmologie (o.a. oogdruppels, droge ogen en artificiële tranen), met focus op OTC‑productenOpbouwen en onderhouden van duurzame relaties met apothekers en hun teamsNauw samenwerken binnen een stabiel en ervaren teamActief meedenken over groeikansen en het vergroten van het marktpotentieelRealiseren van gemiddeld 6 kwalitatieve bezoeken per dagWat breng jij mee? Je bent matuur, verantwoordelijk en werkt zelfstandigJe wil echt mee het verschil makenJe bent proactief, ondernemend en neemt graag initiatiefJe hebt een commerciële mentaliteit en denkt graag strategisch meeJe communiceert vlot in NederlandsJe spreekt vloeiend EngelsWat hebben we jou te bieden? Een competitief salaris, afgestemd op jouw ervaringEen aantrekkelijk pakket aan extralegale voordelen, inclusief bedrijfswagen met laadkaart, groeps‑ en hospitalisatieverzekering, …Een uitdagende functie met veel autonomie binnen een groeiende en stabiele omgevingGrondige begeleiding en opleiding, zodat je sterk van start kan gaan en je verder kan ontwikkelenKlaar om impact te maken? Solliciteer nu!  #LI-MB1 #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.

Ben jij klaar om jouw commerciële talent in te zetten in de gezondheidssector?Wij zoeken een enthousiaste Junior Farmaceutisch Afgevaardigde die apotheken adviseert en ondersteunt bij de verkoop van probiotica en voedingssupplementen. Wat ga je doen? Promotie en verkoop (selling in & selling out) van onze producten bij apotheken in jouw regioRelaties met bestaande klanten onderhouden en versterkenVerkoopactiviteiten analyseren en rapporterenJouw profiel Bachelor diploma, bij voorkeur in een paramedische richtingEerste ervaring als Medisch of Farmaceutisch AfgevaardigdeCommerciële flair en sterke communicatieve vaardighedenEnthousiast, assertief en leergierigZelfstandig en efficiënt in je aanpakOns aanbod Competitief salarisVast contract van onbepaalde duurBedrijfswagen met laadkaart, GSM-abonnementHospitalisatie- en groepsverzekeringPermanente opleiding en begeleidingKlaar om jouw carrière een boost te geven? Solliciteer vandaag en maak het verschil in de gezondheidssector! #LI-MB1 #LI-CES #LI-DNP IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Location: Flexible – U.S.-based (remote with travel)  About the Role IQVIA is seeking a Principal to join our Global MedTech Consulting Services team. This is a senior, client-facing role responsible for leading complex market research and consulting engagements for U.S. and global medical device and diagnostics companies.The Principal operates as a trusted client advisor, commercial leader, and engagement owner—balancing deep research expertise with strong business judgment, leadership through influence, and personal sales accountability.This role is ideal for an experienced MedTech market research or consulting leader who thrives in ambiguity, can translate complex client problems into actionable solutions, and is motivated by both client impact and business growth. Key Responsibilities Client Leadership & Delivery Lead end-to-end primary market research and consulting engagements, serving as the senior point of contact for clients. Translate ambiguous client questions into clear research objectives, study designs, and insight narratives. Ensure high-quality, on-time, and on-budget delivery of projects, with accountability for overall engagement success. Synthesize qualitative and quantitative findings into clear, executive-ready insights and recommendations. Present findings to senior client stakeholders and guide decision-making discussions. Commercial Ownership & Growth Own a personal sales and revenue target, including new business development and account expansion. Identify opportunities to expand client relationships and bring forward relevant IQVIA offerings across the portfolio. Partner with business development, delivery teams, and subject matter experts to shape proposals and solution designs. Support thought leadership activities, conference participation, and client-facing marketing initiatives. Leadership & Collaboration Operate as a senior leader within cross-functional project teams, influencing without direct authority. Provide clear direction, context, and feedback to project team members to ensure strong execution. Mentor junior team members and contribute to capability building within the MedTech Consulting Services group. Collaborate closely with peers, delivery leadership, and global teams to ensure consistency and quality across engagements. Strategic Thinking Apply strong MedTech industry knowledge to anticipate client needs and emerging market trends. Help shape study approaches, methodologies, and value stories that differentiate IQVIA in the market. Balance client demands with commercial discipline, delivery rigor, and internal standards. Qualifications & Experience Required 15+ years of experience in MedTech market research, consulting, or commercial strategy. Demonstrated success leading complex qualitative and quantitative research engagements. Strong client-facing presence with the ability to engage credibly with senior stakeholders. Proven ability to own revenue targets and contribute to business development. Experience across multiple MedTech therapy areas and modalities. Excellent written, verbal, and presentation skills. Ability to work independently in a matrixed organization. Preferred Advanced degree (MMR, MBA, PhD, or equivalent). Experience on both the client and consulting/supplier side. Global project experience and comfort working with international teams. Prior experience within a large professional services organization. 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 $140,200.00 - $390,600.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Location: Valencia, Spain | Experience: 8 Years | Languages: Spanish & English Role Overview The HIS & RCM Implementation Lead is responsible for end-to-end implementation of Hospital Information Systems (HIS) and Revenue Cycle Management (RCM) solutions across healthcare facilities. The role ensures successful delivery aligned with client expectations, timelines, and quality standards. The candidate will act as the primary point of contact in Valencia and lead coordination across stakeholders and teams. Key Responsibilities Lead full lifecycle HIS and RCM implementation including planning, design, build, testing, deployment, and go-live support Manage timelines, deliverables, and dependencies for successful project execution Engage with client stakeholders and provide executive-level reporting Ensure alignment with clinical workflows and revenue cycle processes Lead cross-functional teams across business and technical domains Identify and mitigate risks, issues, and project dependencies Support change management, user adoption, and post-go-live stabilization Required Qualifications Minimum 8+ years of experience in healthcare IT with focus on HIS and RCM Proven experience in large-scale hospital or healthcare implementations Strong understanding of clinical workflows and revenue cycle processes Experience with systems such as Cerner, Epic, or similar platforms Strong leadership and stakeholder management skills Language & Location Requirements Fluent Spanish and English (mandatory) Based in Valencia, Spain with on-site presence during key phases Core Competencies Leadership and decision-making Executive communication skills Accountability and ownership Problem-solving and analytical thinking 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. At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi-talented collaboration harnesses innovation to deliver superior outcomes. Likewise, as part of this culture, IQVIA is committed to ensuring effective equality between women and men, integrating it as a strategic principle in its corporate and human resources policies.

IQVIA™ – The Human Data Science Company™ – ist ein führender, globaler Anbieter von zukunftsweisender Analytik, Technologielösungen und klinischer Auftragsforschung. IQVIA unterstützt Life Science Unternehmen, Verbände, Institutionen, Kostenträger und weitere Akteure im Gesundheitswesen darin, bessere Ergebnisse in der Gesundheitsversorgung zu erzielen. Werden Sie Teil unserer Community von rund 88.000 Mitarbeiterinnen und Mitarbeitern in über 100 Ländern, die sich dafür einsetzen, das Potenzial von Human Data Science Wirklichkeit werden zu lassen! Ganz gleich, in welche Rolle Sie bei IQVIA einsteigen, es erwartet Sie ein offenes, innovationsfreudiges Umfeld, in dem Sie sich viel bewegen können. Finden Sie heraus, wie Sie Ihre Talente und Ihre Leidenschaften bei IQVIA einbringen können. Im Bereich Commercial Engagement Services (CES) arbeiten wir eng mit unseren Life Sciences-Kunden zusammen und unterstützen sie mit flexiblen Vertriebs- und Personallösungen für nachhaltigen Erfolg am Markt. Dies umfasst insbesondere die Rekrutierung, das Training und die Steuerung des Vertriebsteams in Dienstleistungsprojekten bzw. in Arbeitnehmerüberlassung. Dabei differenzieren wir uns über integrierte Projektansätze entlang des IQVIA Lösungsportfolios, die wir individuell an die Kundenbedürfnisse anpassen und aus einer Hand anbieten. Für ein spannendes Projekt suchen wir Pharmaberater (m/w/d) zum nächstmöglichen Zeitpunkt für den Arzt-Außendienst Kardiologie, Pneumologie Im Gebiet: Stuttgart, Tübingen, Burladingen Das sind Deine Aufgaben: Du besuchst nach einer umfangreichen Produktschulung regelmäßig die niedergelassenen Ärzte Ihres Indikationsgebietes (u. a. Atemwegserkrankungen) sowie Fach- und Klinikärzte, um diese über die Kundenprodukte zu informieren und zu beraten. Zu deinen Aufgabenfeldern gehört neben der Organisation ärztlicher Fortbildungs-veranstaltungen auch die Teilnahme an Ärztekongressen und Zyklustagungen. Wiederkehrende Weiterbildungen in deiner Region sowie der aktive Austausch im Team bietet dir die Chance auf eine erfolgsorientierte Entwicklung im Außendienst. Neben der Besprechung von innovativen Produkten hast du als Pharmareferent die Möglichkeit, neuartige Plattformen der Kommunikation zwischen Arzt und Patient zu etablieren. Das bringst Du mit: Du verfügst über eine Naturwissenschaftliche Ausbildung (idealerweise Hochschulabschluss) oder Ausbildung zum Geprüften Pharmareferent (m/w/d) gemäß §75 AMG. Als durchsetzungsstarke Persönlichkeit und erfahrener Netzwerker verstehst du es, deine Ansprechpartner zu begeistern. Du möchtest etwas bewegen – für dein Präparat, für dich selbst und vor allem für betroffene Patienten. Du hast Ausgeprägte kommunikative Fähigkeiten, soziale Kompetenz und bringst die Bereitschaft mit, eigenverantwortlich und ergebnisorientiert zu arbeiten. Das erwartet Dich bei uns: Ein attraktives Gehaltspaket plus Kundenprämien, vielfältige Corporate Benefits, betriebliche Altersvorsorge sowie 24/7 Unfallversicherung (auch für den privaten Bereich) und exklusive private Krankenzusatzversicherungen Ein top ausgestatteter Firmenwagen verschiedener Premiumanbieter mit uneingeschränkter Privatnutzung (ohne Zuzahlung) und mit Wahlmöglichkeit des Modells Eine moderne IT-Ausstattung für Deinen modernen digitalen Arbeitsplatz Unser unbefristetes IQVIA Arbeitsverhältnis bietet Sicherheit und eine langfristige Perspektive Wir bieten u.a. tarifliche Sonderurlaubstage, Umzugszuschuss bei betrieblich bedingtem Wechsel deines Wohnorts Eine hohe Übernahmequote durch unsere Kunden ermöglicht Dir den Karrierestart bei zukunftsweisenden und führenden Unternehmen der Pharmabranche und Medizintechnik-Branche Vielfältige und individuelle Weiterentwicklungsmöglichkeiten auch innerhalb von IQVIA (z.B. Führung, Key Account Management, Projektmanagement und vieles mehr) Wir begleiten Dich während Deiner Bewerbungsphase durch individuelle Betreuung/Vorbereitung bis zur Einstellung und auch darüber hinaus während des Beschäftigungsverhältnisses Unser Kunden-Netzwerk reicht vom Start-up Unternehmen bis zum Global Player. Gemeinsam mit Dir finden wir den richtigen Job für Dich! Starte Deine Karriere mit IQVIA! Dein besonders schneller Draht zu uns: Kandidaten-Hotline: 0621-84508113 oder sende uns gerne direkt Deine Bewerbung per Mail an: [email protected] #LI-CES #LI-DNP #LI-SS2 #Pharmaberater #Biologie #Chemie #Pharmareferent #BTA #CTA #PTA #Oecotrophologie #Pharmazie #Pharma-Außendienst #b-c-a-g 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.

Title:  Sr Prod Data Input Assoc GRE120 Role Purpose: Under guidance maintains more complex reference files needed by IQVIA production. Principal Accountabilities: This position will support the current Outlet Reference team lead in all Outlet activities.Perform maintenance of reference data (Pharmacy, Hospital, Outlet, NDF, TAPS and OneKey) as required for AU/NZ Production and will take on additional geocoding tasks within MapInfo application. Additional work for editing of Health Care Professional practice addresses to ensure correct brick is assigned.Answer queries thru mailbox in Chemup Outlook from external clientsPerform phone verification of details to validate accuracy of reference data maintained as well as captured client-required details such as pharmacy and hospital.In addition, this team is expected to take the initiative to ensure that TAPS and OneKey are as aligned as possible.Bridges data, comparing incoming transaction data with IQVIA’ reference data files to make a match or bridge between the two.Researches and analyses to gather information from third parties that will augment the completeness or accuracy of IQVIA reference data.Contact data suppliers to ensure data is received on time. Updates IQVIA reference file(s) and databases.Follows standard practices and procedures in analyzing situations or data from which answers can be readily obtained.Solicits information from other IQVIA departments to identify when and how to correct inaccurate data, delete data, or add new entries to make the reference files more complete.Receives input to the reference process from other IQVIA production processes.Validates that the information gathered from third-party sources represents accurate new data that should result in a change, addition, or deletion in IQVIA’s existing reference data.Identifies required changes to the existing reference file.Minimum Education, Experience, & Specialized Knowledge Required:Bachelor’s degree of any field.Proficient in Microsoft Excel and Access, with an understanding of relational databasesProficient running SQL queries is a plus.Ability to resolve basic problems pertaining to database issues.Has initiative and is self-motivated to see through until resolution concerns raised by Clients.Strong interpersonal and written and verbal communication skills.Experience in handling inbound and outbound Australian voice accounts.Ability to learn new applications and knows how to multi-task as the job requires.Time Management skills and ability to work independently.Strong customer focus, an attention to detail and excellent critical thinking and problem-solving skillsAbility to proactively identify complex problems and needs and develop solutions/recommendations to solve problems.Organization Reporting and Scope: Typically reports to: Team Lead, Production Additional Requirements: The job requires flexibility to transition to a new project will require quick grasp on different processes from time to time. General knowledge of the company's products and pharmaceutical industry or field specific to a major function. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Join the Angels Initiative Team Today! Every 30 minutes, a stroke patient who could have been saved dies or is permanently disabled because they were treated in the wrong hospital. Our mission is simple: to increase the number of patients treated in stroke-ready hospitals and to optimize the quality of treatment in all existing stroke centers. We are building a global community of stroke centers and stroke-ready hospitals, working every day to improve the quality of treatment for every stroke patient. This is a unique opportunity to join IQVIA in partnership with Boehringer Ingelheim to improve stroke care worldwide through a corporate social responsibility project. We are looking for an Angels Consultant based in Bulgaria who will join an exciting working environment in a dynamic and international atmosphere. ResponsibilitiesIncrease efficiency in the management of stroke patients. Support hospitals and healthcare professionals with continuous training and organizational tools. Serve as an expert Therapeutic Consultant, promoting new diagnostic and treatment guidelines to hospitals. Foster and promote quality monitoring programs to maintain consistent hospital performance. Expand the project's reach to new hospitals. Lead multidisciplinary stroke teams through continuous improvement. Enhance therapeutic protocols in major hospitals. Required SkillsProven experience in pharmaceutical sales (preferably related to neuroscience or stroke care). Excellent scientific background. A PhD in Neuroscience or a related field is desirable, but not required. Strong interpersonal skills and high motivation. Fluency in English (Bulgarian language fluency is required) Leadership abilities. Proactivity, flexibility, and problem-solving skills. Valid driving license and willingness to travel up to 70% of the time. #LI-CES #LI-CS1 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.

About the Role As a Clinical Process Coordinator, you’ll support clinical research projects by ensuring smooth processes and accurate documentation. This is an administrative role within our global team, perfect for early-career professionals ready to learn and gradually grow their career in the pharmaceutical and clinical research industry. The role is hybrid, with 2 days/week obligatory presence in our office in Sofia, Bulgaria. What You’ll Do Track site visits in CTMS and update systems to keep records accurate.Work with Trial Master File (TMF), perform file reviews and documents uploads.Help set up vendors and review invoices for correctness.Manage access for team members and Review ATP (Authorization to proceed) trainings.Coordinate translations for study documents with our vendors.Review contracts and support teams to deliver high-quality work.Work closely with project managers and other teams to resolve queries quickly.Respond to requests for data or reports when needed.Provide general administrative support and keep activities organized.What We’re Looking For: Education Life sciences graduate (experience in pharma industry is a plus).Skills Knowledge of MS Office and data processing.Fluent in English and Bulgarian.Fast learner with strong communication skills.Ability to prioritize and coordinate multiple tasks to meet deadlines.Professional approach and willingness to learn.Work Style Ability to build effective relationships with colleagues and clients.Comfortable working in a hybrid model (at least 2 days/week in our Sofia office).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 a motivated and results-driven Pharmaceutical Sales Representative to join our team. In this role, you will be responsible for driving volume and market share growth for assigned pharmaceutical products within a designated territory. You will build strong relationships with healthcare professionals and deliver impactful sales presentations in an office-based setting. Key Responsibilities Include: Generating volume and market share growth for assigned pharmaceutical products within a specific geographic area. Selling presentations to physicians and other health care professionals, primarily in an office-based setting. Developing an understanding of the issues and opportunities unique to the geography, particularly in managed health care. Manage allocated resources (samples, promotional and educational materials) to maximize return within regulatory and ethical guidelines. Maintains accountability for all pharmaceutical samples in accordance with FDA and PDMA guidelines. Utilize the sales automation system to document call and program activity. Complete initial and ongoing product and development training as required.Requirements: BA/BS requiredPreferred: Minimum of 2 years business-to-business outside sales experience with demonstrated record of impact preferred. 1-2 years of Pharmaceutical Sales experience with demonstrated record of impact preferredEstablished relationships within targeted geography.Key Competencies: Sales ability/persuasiveness, use of appropriate interpersonal style and communication methods to facilitate an acceptance of an idea, plan, activity or product from targeted customers.Establishes account plans based on customer needs and business priorities.Establishes method for monitoring progress to goals.Must set high goals or standards of performance, self-starter, able to work independently.Must demonstrate ability to influence events to achieve goals and take actions beyond what is required in being proactive.Must be able to utilize resources and create a positive/professional impression, commanding attention and respect, displaying confidence.Ability to maintain effectiveness in varying environments and with different tasks, responsibilities and people is key.Must express ideas effectively in individual and group situations, adjusting to the characteristics or needs of the target audience#LI-CESIQVIA 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 $80,000-115,000 annually. 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.

Position Title: Mobile Nurse (LPN/LVN) – Per Diem, In-Home Services    Location: Various U.S. locations (local travel within designated geographic area)    About the Role: IQVIA’s In-Home Clinical Solutions team seeks a qualified and dedicated Mobile Licensed Practical Nurse (LPN) or Licensed Vocational Nurse (LVN) to deliver in-home clinical services to patients initiating therapy with complex medications. This per diem role involves traveling to patient residences to perform clinical services such as, but not limited to, phlebotomy, electrocardiograms (EKGs), and macular edema screenings in support of treatment initiation and adherence strategies.    This is a per diem, travel-based role offering flexible hours, with no minimum monthly visit requirement. Referrals are assigned based on your geographic availability and program demand. IQVIA manages all scheduling and patient communication, allowing you to focus entirely on clinical care.     Position Details:  Per diem, mobile-based role with flexible scheduling  No minimum monthly visit commitment required  Paid hourly compensation that includes the appointment time and travel time to/from patient’s home. (2 hour minimum paid)  IRS-standard mileage rate reimbursement.    Key Responsibilities:  Perform in-home blood specimen collection, labeling, and transporting specimens according to network policies, procedures, and regulatory standards.  Comply with all laboratory safety and handling procedures; ensure appropriate delivery to designated laboratories.  Conduct screenings as has been appropriately trained to conduct, including but not limited to electrocardiograms (EKGs) and macular edema screening exams (training provided).  Maintain a clean and organized work environment, including transportation and supplies storage specific to the In-Home Network.  Monitor and manage clinical supply inventory.  Collaborate with IQVIA’s clinical coordination team to execute and submit appropriate visit-related paperwork promptly and accurately.   Identify and report adverse events, medical product complaints, or patient inquiries in accordance with IQVIA and manufacturer guidance.  Maintain accurate mileage and time logs for reimbursement and compliance purposes.    Qualifications:  Active and unrestricted LPN or LVN license required  Current CPR certification required  Minimum 2 years of phlebotomy experience in clinical or field settings required  At least 1 year of EKG experience preferred  Certification as a Certified Medical Assistant (CMA) or Phlebotomy Technician (CPT) preferred.  Ability to lift up to 70 pounds to transport medical or diagnostic equipment (e.g., eye exam kits).  Ability and willingness to travel up to 100 miles to conduct patient visits.  Proficiency in using medical equipment and upholding proper documentation practices.  Strong interpersonal and communication skills with a patient-focused approach.  Fluent in spoken and written English.  Must possess a valid driver’s license and will be subject to a review of driving record prior to hire.  Must complete a drug screening and background check after accepting an offer.    #LI-CES  #LI-DNP  IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is 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 28.00 per hour. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Position Title: Mobile Medical Assistant / Phlebotomist – Per Diem, In-Home Services    Location: Various U.S. locations (local travel within designated geographic area)    About the Role: IQVIA’s In-Home Clinical Solutions team seeks a qualified and dedicated Mobile Medical Assistant / Phlebotomist to support patient care by delivering in-home diagnostic services. This per diem role involves traveling to patient residences to perform clinical services such as, but not limited to, phlebotomy, electrocardiograms (EKGs), and macular edema screenings in support of treatment initiation and adherence strategies.    This is a per diem, travel-based role offering flexible hours, with no minimum monthly visit requirement. Referrals are assigned based on your geographic availability and program demand. IQVIA manages all scheduling and patient communication, allowing you to focus entirely on clinical care.    Position Details:  Per diem, mobile-based role with flexible scheduling  No minimum monthly visit commitment required  Paid hourly compensation that includes the appointment time and travel time to/from patient’s home. (2 hour minimum paid)  IRS-standard mileage rate reimbursement.    Key Responsibilities:  Perform in-home blood specimen collection, labeling, and transporting specimens according to network policies, procedures, and regulatory standards.  Comply with all laboratory safety and handling procedures; ensure appropriate delivery to designated laboratories.  Conduct screenings as has been appropriately trained to conduct, including but not limited to electrocardiograms (EKGs) and macular edema screening exams (training provided).  Maintain a clean and organized work environment, including transportation and supplies storage specific to the In-Home Network.  Monitor and manage clinical supply inventory.  Collaborate with IQVIA’s clinical coordination team to execute and submit appropriate visit-related paperwork promptly and accurately.   Identify and report adverse events, medical product complaints, or patient inquiries in accordance with IQVIA and manufacturer guidance.  Maintain accurate mileage and time logs for reimbursement and compliance purposes.     Qualifications:  Minimum 2 years of phlebotomy experience in clinical or field settings required  At least 1 year of EKG experience preferred  Certification as a Certified Medical Assistant (CMA) or Phlebotomy Technician (CPT) preferred.  If located in the state of Washington or Louisiana, a state issued CMA or CPT license is required.  Ability to lift up to 70 pounds to transport medical or diagnostic equipment (e.g., eye exam kits).  Ability and willingness to travel up to 100 miles to conduct patient visits.  Proficiency in using medical equipment and upholding proper documentation practices.  Strong interpersonal and communication skills with a patient-focused approach.  Fluent in spoken and written English.  Must possess a valid driver’s license and will be subject to a review of driving record prior to hire.  Must complete a drug screening and background check after accepting an offer.    #LI-CES  #LI-DNP  IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role is 25.00 per hour. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Valorizamos a diversidade e acreditamos em equipes inclusivas. Por isso, esta é uma vaga afirmativa destinada a pessoas com deficiência (PCDs).Responsabilidades: Aprovação do registro contábil e pagamentos de notas fiscais de fornecedores, taxas e impostos.Realizar lançamentos contábeis de notas fiscais de serviços, produtos e demais documentos.Verificar pendências de notas fiscais e apoiar na tratativa de inconsistências.Efetuar provisões, reversões, antecipações, pro-rata, alocação correta por centro de custo e projetos.Conhecimento processuais bancários como liquidação de pagamentos e conciliações.Requisitos: Experiência prévia em lançamentos de notas fiscais e impostos.Ensino Superior cursando ou completo em Ciências Contábeis, Administração ou correlatos.Necessário conhecimento no pacote Office, mandatório Excel intermediário;Conhecimento em contabilidade geral, conciliações e classificações contábeis.Noções de impostos retidos e legislação fiscal.Desejável: conhecimento em sistemas ERP (SAP e Dzyon), assim como inteligência artificial e Power BI.Laudo atualizado para enquadramento.Competências desejadas: Organização e atenção aos detalhes.Capacidade analítica.Proatividade e vontade de aprender.Boa comunicação e trabalho em equipe. Hands on, owernship e autodireção a processo operacional.Habilidade de interações em grupos multifuncional e multidisciplinar.IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

IQVIA™ – The Human Data Science Company™ – ist ein führender, globaler Anbieter von zukunftsweisender Analytik, Technologielösungen und klinischer Auftragsforschung. IQVIA unterstützt Life Science Unternehmen, Verbände, Institutionen, Kostenträger und weitere Akteure im Gesundheitswesen darin, bessere Ergebnisse in der Gesundheitsversorgung zu erzielen. Werden Sie Teil unserer Community von rund 88.000 Mitarbeiterinnen und Mitarbeitern in über 100 Ländern, die sich dafür einsetzen, das Potenzial von Human Data Science Wirklichkeit werden zu lassen! Ganz gleich, in welche Rolle Sie bei IQVIA einsteigen, es erwartet Sie ein offenes, innovationsfreudiges Umfeld, in dem Sie sich viel bewegen können. Finden Sie heraus, wie Sie Ihre Talente und Ihre Leidenschaften bei IQVIA einbringen können. Im Bereich Commercial Engagement Services (CES) arbeiten wir eng mit unseren Life Sciences-Kunden zusammen und unterstützen sie mit flexiblen Vertriebs- und Personallösungen für nachhaltigen Erfolg am Markt. Dies umfasst insbesondere die Rekrutierung, das Training und die Steuerung des Vertriebsteams in Dienstleistungsprojekten bzw. in Arbeitnehmerüberlassung. Dabei differenzieren wir uns über integrierte Projektansätze entlang des IQVIA Lösungsportfolios, die wir individuell an die Kundenbedürfnisse anpassen und aus einer Hand anbieten. Für ein spannendes Projekt suchen wir Pharmaberater (m/w/d) zum nächstmöglichen Zeitpunkt für den Facharzt-Außendienst Kardiologie, Pneumologie Im Gebiet: Rostock, Stralsund, Lübeck, Parchim Das sind Deine Aufgaben: Du besuchst nach einer umfangreichen Produktschulung regelmäßig die niedergelassenen Ärzte Ihres Indikationsgebietes (u. a. Atemwegserkrankungen) sowie Fach- und Klinikärzte, um diese über die Kundenprodukte zu informieren und zu beraten. Zu deinen Aufgabenfeldern gehört neben der Organisation ärztlicher Fortbildungs-veranstaltungen auch die Teilnahme an Ärztekongressen und Zyklustagungen. Wiederkehrende Weiterbildungen in deiner Region sowie der aktive Austausch im Team bietet dir die Chance auf eine erfolgsorientierte Entwicklung im Außendienst. Neben der Besprechung von innovativen Produkten hast du als Pharmareferent die Möglichkeit, neuartige Plattformen der Kommunikation zwischen Arzt und Patient zu etablieren. Das bringst Du mit: Du verfügst über eine Naturwissenschaftliche Ausbildung (idealerweise Hochschulabschluss) oder Ausbildung zum Geprüften Pharmareferent (m/w/d) gemäß §75 AMG. Als durchsetzungsstarke Persönlichkeit und erfahrener Netzwerker verstehst du es, deine Ansprechpartner zu begeistern. Du möchtest etwas bewegen – für dein Präparat, für dich selbst und vor allem für betroffene Patienten. Du hast Ausgeprägte kommunikative Fähigkeiten, soziale Kompetenz und bringst die Bereitschaft mit, eigenverantwortlich und ergebnisorientiert zu arbeiten. Das erwartet Dich bei uns: Ein attraktives Gehaltspaket plus Kundenprämien, vielfältige Corporate Benefits, betriebliche Altersvorsorge sowie 24/7 Unfallversicherung (auch für den privaten Bereich) und exklusive private Krankenzusatzversicherungen Ein top ausgestatteter Firmenwagen verschiedener Premiumanbieter mit uneingeschränkter Privatnutzung (ohne Zuzahlung) und mit Wahlmöglichkeit des Modells Eine moderne IT-Ausstattung für Deinen modernen digitalen Arbeitsplatz Unser unbefristetes IQVIA Arbeitsverhältnis bietet Sicherheit und eine langfristige Perspektive Wir bieten u.a. tarifliche Sonderurlaubstage, Umzugszuschuss bei betrieblich bedingtem Wechsel deines Wohnorts Eine hohe Übernahmequote durch unsere Kunden ermöglicht Dir den Karrierestart bei zukunftsweisenden und führenden Unternehmen der Pharmabranche und Medizintechnik-Branche Vielfältige und individuelle Weiterentwicklungsmöglichkeiten auch innerhalb von IQVIA (z.B. Führung, Key Account Management, Projektmanagement und vieles mehr) Wir begleiten Dich während Deiner Bewerbungsphase durch individuelle Betreuung/Vorbereitung bis zur Einstellung und auch darüber hinaus während des Beschäftigungsverhältnisses Unser Kunden-Netzwerk reicht vom Start-up Unternehmen bis zum Global Player. Gemeinsam mit Dir finden wir den richtigen Job für Dich! Starte Deine Karriere mit IQVIA! Dein besonders schneller Draht zu uns: Kandidaten-Hotline: 0621-84508113 oder sende uns gerne direkt Deine Bewerbung per Mail an: [email protected] #LI-CES #LI-DNP #LI-SS2 #Pharmaberater #Biologie #Chemie #Pharmareferent #BTA #CTA #PTA #Oecotrophologie #Pharmazie #Pharma-Außendienst #b-c-a-g 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.