IQVIA

【会社紹介・ビジョン】  私たちIQVIAは、ヒューマンデータサイエンスの先駆的な企業として、医療・ヘルスケアの前進に取り組む皆様をIQVIAならではの革新的なソリューションによってご支援することで、「誰もが、より健康に自分らしく生きられる社会」の実現を目指しています。世界最大規模を誇る医療・ヘルスケア関連データを基盤に、人・データ・サイエンスを融合させた見地から、未だ満たされない治療ニーズに応える、新たな医薬品や医療機器の開発と市販化、厳格化する規制やコンプライアンスへの対応、持続可能な医療システム推進の支援など、患者さんをはじめとするすべての人々のために、より良い未来へと医療・ヘルスケアを前進させていく力となることが、私たちの使命です。  世界100以上の国と地域で約9万人が活動するIQVIAの日本法人として、IQVIAジャパンでは約6,000人が一丸となり、この使命に向かって日々、力を尽くしています。 【部署・チーム名】  グローバルで先行していた「RADDS」（Regulatory Affairs & Drug Development Solutions）と呼ばれる新組織を日本でも始動。顧客のニーズに応じて薬事対応、開発戦略立案、臨床開発などのサービスを一体的に提供する体制を構築しました。グローバルとも連携して海外の新興バイオファーマ（EBP）を日本に呼び込むとともに、日本のバイオベンチャーの海外開発・申請をサポートします。RADDS Japan was established to support EBP initiative for business growth in RD&S. This position requires the successful candidate to support the activities in RADDS Japan which includes contributing to the scoping, integrated proposal compilation, and delivery oversight of multi-disciplinary biopharmaceutical development advisory/clinical trial enablement projects.【業務内容】 ・Manage staff in accordance with organization’s policies and applicable regulations; Responsibilities include planning, assigning, and directing work; appraising performance and guiding professional development; rewarding and disciplining employees; addressing employee relations issues and resolving problems; Approve actions on human resources matters, including salary administration. ・Effectively manages the team's resources and delegates tasks commensurate with skill level; Evaluates workload, quality and metrics through regular review and reporting of findings; Effectively collaborate with operational colleagues to manage project- and team-related challenges; Contributes to discussions on implementation of business strategy on a regional basis and will implement regional and global specific objectives, as appropriate. ・Ensures staff have a consistent understanding and positive impression of strategy for regional and global objectives; Leads strategic initiatives and develops implementation plans; ・Will have full financial responsibility and accountability for one or more Regulatory Affairs sites; monitors growth and performance of the sites; Undertakes risk analysis and manages the outcome as appropriate; ・May act as a Project Manager for a large and complex stand-alone project or programme, involving several regulatory or technical deliverables and/or region, and/or operations; ・May provide strategic regulatory and/or technical consultancy on a variety of projects; •Competently manages meetings/expectations with Regulatory Agencies and/or groups within IQVIA; •May take leadership role in bid defense strategy and planning; •May lead/chair a session on Regulatory Affairs or related topics at a conference; deliver effective presentations to a broad audience; メーカーやCROでの薬事経験者 ラインマネジメントの経験 ・At least 8 years regulatory experience including 6 years management experience. ・Requires broad management knowledge to lead teams, and well as the ability to influences others outside of own job area regarding policies, procedures, and goals. ・Possess demonstrated working knowledge of corresponding professional grade level responsibilities, skills and abilities, as required for guidance of staff Line management experience required, with demonstrated success in development, engagement and performance of senior staff. ・Advanced negotiating and influencing skills and the ability to identify and resolve issues, using flexible adaptable approach.  Remains calm, assertive and diplomatic in challenging interactions with customers and staff ・Possesses an acute awareness of issues outwith the business function.  Exudes confidence and authority within remit, and delivers a positive example to teams ・Communicates an inspiring vision of the Regulatory Strategic Plan and helps others understand and value their role in it. ・Ability to work effectively with senior management, remaining motivated and enthusiastic in times of change and other pressure situations 【部署・ポジションの醍醐味、楽しさ、やりがい】 ・有用な医薬品の早期の開発、承認に貢献できる・再生医療を含む、最先端の医療へ関与できる・Projectをリードし、クライアントとのコミュニケーションを含め、自己完結で業務遂行できる・様々な領域（治療領域、生物的製剤、再生医療等）での経験が積める 【特別な研修・サポート制度等】 ・英語研修・GCPなど各種社内外研修・医薬品開発に関する部内外研修・学会への参加 【雇用形態・勤務時間・福利厚生・休日休暇】  雇用形態：正社員／契約社員など  勤務時間：9:00-17:30   フレックス勤務：あり  在宅勤務制度：あり 福利厚生：法定内（社会保険制度）・法定外（IQVIA独自制度）の両面から充実した福利厚生制度あり  受動喫煙対策：あり  休日休暇：年次有給休暇、夏季休暇、病気休暇、特別休暇、女性特別休暇、育児介護休暇、看護休暇·など  試用期間：あり（通常６か月）  【給与・待遇】  給与：当社規定により優遇します  昇給：あり  賞与：あり  時間外手当：あり  【選考プロセス】  書類選考→部門とのカジュアル面談→応募後、部門面接（3回あり） 【応募方法】  日本語の履歴書、職務経歴書、英語職務経歴書の3点をご準備ください。 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

Project Role: Programmer Work Experience: 5 to 10 Years Work location: Bengaluru. Work Mode: Remote Must Have Skills: Data Acquistion, , data transfer, handling blinded data, quality assessments. Job Overview: • Plan and coordinate database design, development, implementation, maintenance, and user support of clinical systems. • Provide technical expertise in conjunction with internal and external clients. • Program, test, and document databases in accordance with programming standards and validation procedures. • Good in working on Data Acquisition activities like creation of vendor specification, data transfer, handling blinded data, quality assessments. • Program database manipulation and transfers of data for internal and external clients. • May assist IT in developing and implementing new technologies. • May assist IT in testing and evaluating new upgrades to technologies. • May assist in developing, revising, and maintaining core operating procedures and working instructions. • Good in creating/updating the program/report based on requirement on report management system (RMS). • Meet objectives as assigned, and interact with the project team to organize timelines, responsibilities and deliverables. • Develop and maintain good communications and working relationships with teams and external clients. • May interact with corporate team and CDM team members to negotiate timelines, responsibilities,and deliverables.• May serve as Lead Programmer on the corporate team.Required Knowledge, Skills And Abilities:• Bachelor's Degree Computer/life science or related field Req• Equivalent combination of education, training and experience in lieu of degree Req• Working knowledge of a relational database, electronic data capture and/or other relevant datamanagement technologies• Good knowledge of SAS/SQL/Python tool• Good understanding of regulations including ICH-GCP/21 CFR part 11• Good conceptual, organizational and communication skills• Ability to establish and maintain effective working relationships with coworkers, managers andclients  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 Description • Bridges data into IQVIA systems • Bridges data, compares incoming transaction data with IQVIA’s reference data files to make a match or bridge between the two • Performs quality assurance on bridged data to ensure it accurately reflects paper data/electronic files submission • Quality checks of data coded in offshore team to preserve proper QA • Analyze rejected records from production to assign bridge status • Updates and checks bridge status and updates factoring changes • Modifies bridge tables according to business rules Job Requirements:• Bachelor’s degree in any Science and Technology field• Proficient in Microsoft office applications• Good English communication skills both oral and written• Good Analytical Skills• Able to adapt to new environments and production processes• Uses own initiative, be a self-starter and be able to learn new skills• A Team player who is inquisitive and challenges different solutions 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 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.

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.

Internal Job DescriptionJob OverviewUnder supervision, provide support enabling the accurate and timely payment administration to our network of project sites.  Perform duties in accordance with IQVIA Finance Standard Operating Procedures (SOPs), Sarbanes-Oxley Controls and Unit Service Level agreements (if applicable).  Essential Functions Managing a portfolio of projects and providing oversight on the entire process. Ability to form remote relationships with colleagues across the globe, consider indirect influences on your work and manage these. Highlighting aged invoices and financial risks – give reasons why for any delays Data quality control, ensuring batches are scheduled as per contracts and meeting the budgets Project reconciliations Payment cycle target trending – ensuring the studies are meeting the target for each step in the payment cycle Providing high level of customer service to internal project teams and assisting them in any project related issues by finding resolution. Ability to influence others and ensure that key actions are taken Track and report metric data flagging nonstandard issues to project teams / line manager Provide assistance to other team members as required, to ensure the group meets targets. Check that appropriate approvals are obtained for set up and payment process. Provide support and participate in teams handling various routine tasks. Provide standard reports and run KPI for the project teams Perform other duties as assigned. File appropriate documents. QualificationsHigh School Diploma or equivalentPrevious experience in systems would be an advantage however full training will be provided 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 us on our exciting journey! IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, Technology, analytics and human ingenuity to drive healthcare forward. Job OverviewIQVIA is seeking a Strategic Pricing Analyst to support the development and optimization of innovative pricing models and analytics that enable transformational deals and drive excellence in strategic pricing and sales operations. This role will collaborate cross-functionally to enhance customer engagement, support technology-driven innovation, and streamline pricing processes using lean principles. Key ResponsibilitiesDevelop and support strategic pricing models that enhance the customer experience and drive commercial excellence.Conduct pricing calculations and determine optimal price levels within established models.Contribute to the definition and evolution of corporate pricing strategies.Perform competitive pricing analyses to support go-to-market strategies and internal governance.Provide guidance and support to team members on pricing-related matters.Collaborate with cross-functional teams to ensure alignment and stakeholder engagement.Continuously seek opportunities to improve pricing processes and tools.Perform other related duties as assigned.Qualifications - our ideal candidate will have Bachelor’s degree in Business Management, Economics, Accounting, Marketing, Information Systems, or a related field.Minimum of 3 years of experience in Contracts, Proposals, Business Management, Business Intelligence, IT, or commercial systems technology.Familiarity with the contract research and pharmaceutical development industry.Proficiency in programming and quality control of complex Excel-based pricing solutions.Understanding of costing models and pricing algorithms.Knowledge of system integration between pricing and other business systems.Strong analytical, budgeting, and forecasting skills.Excellent verbal and written communication abilities.Ability to manage complex budgets and identify dependencies within pricing models.Proven ability to build effective working relationships in a high-performance environment.Preferred SkillsExperience with lean process improvement methodologies.Exposure to strategic sales operations or commercial excellence initiatives.Ability to work independently and manage multiple priorities.We know that meaningful results require not only the right approach but also the right people. Regardless of your role, we invite you to reimagine healthcare with us. You will have the opportunity to play an important part in helping our clients drive healthcare forward and Whatever your career goals, we are here to ensure you get there! We invite you to join IQVIA™. 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.

As you develop your career as a Senior CRA or CRA, this role offers you the opportunity to plan and progress your career in the direction you choose. At IQVIA, we do not believe in a ‘career ceiling.’ You will be exposed to wider opportunities like operations management, dedicated customer solutions, project management and more. And you won’t do it alone – you will have dedicated mentoring and receive structured quarterly reviews on performance, promotion opportunities and awards. Joining IQVIA will give you access to cutting-edge in-house technology and provide opportunities to work on global projects/ trials. You will be building a flexible, meaningful and fulfilling career with no limits. Your responsibilities will include: Performing site selection, initiation, monitoring, and close-out visits, plus maintaining appropriate documentation Supporting the development of a subject recruitment plan Establishing regular lines of communication plus administering protocol and related study training to assigned sites Evaluating the quality and integrity of site practices – escalating quality issues as appropriate Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution You will need to be comfortable collaborating and communicating with a variety of colleagues and customers. You will need to have a good knowledge of applicable clinical research regulatory requirements. Qualifications: University degree in scientific discipline or healthcare At least 1 year of on-site monitoring experience Good knowledge of GCP and clinical research regulatory requirements Good computer skills including MS Office Excellent command of English language Organizational, time management and problem-solving skills Ability to establish and maintain effective working relationships with colleagues, managers, and customers. Flexibility to travel. What you can expect: Working with different customers on global trials Career development opportunities for those who are passionate in wanting to grow as part of the organization. Leaders that support flexible work schedules/arrangement Excellent working environment in a stable, international, reputable company Programs to help you build your technical skills, therapeutic knowledge and regular refreshers for updates in the regulatory landscape Attractive remuneration package. #LI-Hybrid 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 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.

Solution Architect - Contracting Technologies Responsibilities: · Lead the design, development, and implementation of Contracting solutions on the Salesforce platform, with a focus on CLM. · Collaborate with business stakeholders to understand their requirements and translate them into technical solutions. · Develop and maintain architectural blueprints, ensuring alignment with business goals and technology standards. · Provide technical leadership and guidance to development teams throughout the project lifecycle. · Conduct solution architecture reviews and ensure best practices are followed. · Integrate Salesforce-based Contracting applications with other enterprise systems and third-party applications. · Stay updated with the latest Salesforce features and trends in Contracting technologies. · Troubleshoot and resolve technical issues related to Contracting solutions on Salesforce. · Mentor and train junior team members on Salesforce and Contracting best practices. Qualifications: · Bachelor’s degree in Computer Science, Information Technology, or a related field. · Proven experience as a Solution Architect with a focus on Salesforce and Contracting technologies, including CLM. · In-depth knowledge of the Salesforce platform, including Sales Cloud, Service Cloud. · Strong understanding of Contracting processes and best practices. · Experience with Salesforce integration tools and techniques (e.g., REST/SOAP APIs, MuleSoft). · Excellent problem-solving skills and the ability to work under pressure. · Strong communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams. · Salesforce certifications (e.g., Salesforce Certified Technical Architect, Salesforce Certified Application Architect) are a plus. Specific responsibilities: · Oversee TPA, AMA, MyCDA, CLM and DocuSign architecture needs · Be the chief technology expert for all these applications IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

Job OverviewAs a Sr Sourcer in Talent Search at IQVIA, you will play a pivotal role in shaping our talent acquisition strategy by partnering closely with recruiters, hiring managers, and business leaders. This role is ideal for a proactive, data-driven, and collaborative professional who thrives in a fast-paced environment and is passionate about identifying top talent to drive business success. Key ResponsibilitiesStrategic Partnership: Collaborate with recruiters and hiring managers across designated departments to understand hiring needs and develop tailored sourcing strategies.Intake Leadership: Lead intake meetings to define role requirements, set expectations, and align on recruitment timelines and goals.Sourcing Strategy Development: Design and execute innovative, cost-effective recruiting plans to attract high-quality candidates.Job Posting Management: Create, publish, and optimize job postings to maximize visibility and attract diverse talent.Candidate Engagement: Leverage platforms such as LinkedIn, job boards, and CRM tools to identify and engage passive candidates, promoting IQVIA’s mission and opportunities.Screening and Evaluation: Review applications, conduct initial interviews, and assess candidates’ qualifications, experience, and alignment with role expectations.Diversity and Compliance: Champion diversity hiring initiatives and ensure adherence to local and regional compliance standards.Market Intelligence: Monitor industry trends and talent market dynamics to inform sourcing strategies and hiring decisions.Data Management: Maintain accurate and up-to-date records in the ATS and CRM systems.Team Collaboration: Partner with the broader recruitment team to ensure a seamless and positive candidate experience.Analytics and Reporting: Use data and metrics to evaluate sourcing effectiveness and continuously improve recruitment strategies.Mentorship: Provide guidance and mentorship to junior Talent Search team members, fostering a culture of learning and excellence.QualificationsBachelor’s degree or equivalent combination of education, training, and experience.Proven experience in a Talent Search or Recruiter role, preferably in a fast-paced, global organization.Strong relationship-building skills with stakeholders at all levels.Demonstrated commitment to continuous learning and staying current with talent acquisition trends.Cultural awareness and sensitivity in a diverse hiring environment.Excellent organizational, time management, and communication skills.Proficiency in Boolean search techniques and sourcing tools.Strong analytical and problem-solving abilities.Adaptability and resilience in a dynamic work environment.Why IQVIA?At IQVIA, we are committed to advancing human health through data science, technology, and deep domain expertise. Join a team that is passionate about innovation, collaboration, and making a meaningful impact on global healthcare. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

As a global leader in commercial solutions, IQVIA is uniquely positioned to deliver results both nationally and internationally. Our teams partner with biopharma companies to bring essential medicines to the people who need them most. We empower our clients with insights and access to their markets, helping them demonstrate the value of their products to payers, physicians, and patients alike. A core part of our mission includes serving as the sales force for biopharma or providing nurse educators who support patients and prescribers. With the right experience, you can help bring medical innovations to life in real-world settings. We’re excited to announce an opportunity to join our team of over 10,000 field professionals worldwide—we’re currently hiring a Nurse Educator to support our pharmaceutical and biotech clients. Nurse Educator At the heart of our business strategies is a commitment to patients. The Nurse Educator Program is a patient-centered, educational initiative designed to support individuals living with chronic conditions who have been prescribed specific therapies. Nurse Educators play a vital role in helping patients understand their treatment, manage their condition, and access relevant resources related to their prescribed medication. This role involves one-on-one engagement with patients through various channels, including in-person visits, phone calls, video conferencing, email, and SMS—always in strict alignment with program guidelines. Please note: this is an educational role only. Nurse Educators do not provide clinical care or medical advice. Role Overview: Nurse Educator As a Nurse Educator, you will play a key role in supporting patients by connecting them with program-approved resources and delivering personalized education on chronic disease management and prescribed therapies. This role is designed to empower patients, promote treatment adherence, and encourage meaningful dialogue with healthcare providers. Key Responsibilities Facilitate connections between patients and approved educational resources. Deliver direct, disease-specific education and training related to prescribed medications. Support multiple disease states and therapies as needed. Promote behavioral change through patient-centered education to improve treatment adherence. Encourage effective communication between patients and their healthcare providers. Qualifications Bachelor’s degree and/or BSN preferred. Active RN license in state of residence; compact multi-state license preferred where applicable. Nursing license must be current and in good standing. Minimum of 5 years of clinical experience in healthcare (hospital, home health, pharmaceutical, or biotech settings). Prior experience as a nurse educator is preferred. Bilingual in English and Spanish is a plus. Valid driver’s license required. Must reside within the designated territory. Experience in direct patient interaction with a focus on adherence and persistence. Strong understanding of clinical data and pharmacology. Excellent time management, planning, and multitasking skills. Effective presentation and motivational skills; strong interpersonal and communication abilities. Ability to work independently and cross-functionally. Dedicated home workspace required. Adaptability to changing responsibilities and environments. Proficiency in Microsoft Office (Word, Excel, PowerPoint) and iPad technology. Flexibility to work evenings and weekends as needed. Willingness to travel up to 60–70%. Compliance with client vaccination requirements may be necessary. Compensation Competitive annual salary Car allowance Bonus eligibility  #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 $115,000-$120,000 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.

Job OverviewProvides high quality, on-time input to client projects in the life sciences field. Assignments typically require analysis and problem solving within an established framework. Essential Functions• Under direct supervision, assists with the review and analysis of client requirements or problems and assists in the development of client solutions.• Assists in the development of detailed documentation and specifications.• Under close supervision, performs quantitative or qualitative analyzes to assist in the identification of client issues and the development of client specific solutions.• Assists in the design and structure of presentations that are appropriate to the characteristics or needs of the audience.• Proactively develops a basic knowledge of consulting methodologies and the life sciences market through the delivery of consulting engagements and participation in formal and informal learning opportunities.• Engagement based responsibilities are assigned and closely managed by Consultants, Senior Consultants, Engagement Managers or Principals. Qualifications• Bachelor's Degree  Req• 1-3 years of related experience Req• Works willingly and effectively with others in and across the organization to accomplish team goals.• Knowledge and understanding of the fundamental processes of business, their interaction, and the impact of external/internal influences on decision making, growth and decline.• Knowledge of consulting methods, tools and techniques, related to one’s functional area.• Knowledge of current events and developments within an industry and major competitors.• Knowledge and understanding of the marketplace. Knowledge of professional/trade associations, key people and companies.• Effective time management skills. 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 high quality, on-time input to client projects in the life sciences field. Assignments typically require analysis and problem solving within an established framework. Essential Functions• Under direct supervision, assists with the review and analysis of client requirements or problems and assists in the development of client solutions.• Assists in the development of detailed documentation and specifications.• Under close supervision, performs quantitative or qualitative analyzes to assist in the identification of client issues and the development of client specific solutions.• Assists in the design and structure of presentations that are appropriate to the characteristics or needs of the audience.• Proactively develops a basic knowledge of consulting methodologies and the life sciences market through the delivery of consulting engagements and participation in formal and informal learning opportunities.• Engagement based responsibilities are assigned and closely managed by Consultants, Senior Consultants, Engagement Managers or Principals. Qualifications• Bachelor's Degree  Req• 1-3 years of related experience Req• Works willingly and effectively with others in and across the organization to accomplish team goals.• Knowledge and understanding of the fundamental processes of business, their interaction, and the impact of external/internal influences on decision making, growth and decline.• Knowledge of consulting methods, tools and techniques, related to one’s functional area.• Knowledge of current events and developments within an industry and major competitors.• Knowledge and understanding of the marketplace. Knowledge of professional/trade associations, key people and companies.• Effective time management skills. 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 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.

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.

Key Account Representative In partnership with our client, we are actively searching for Key Account Representatives to deliver on our commitment to serve patients. The Key Account Representative will be responsible for promoting a product to specialty healthcare providers in an assigned territory. Qualifications/Experience: 4-year degree from an accredited college or university required 2 years B2B sales experience preferred 1 year of pharmaceutical or med device sales experience a plus Device or diagnostic experience a plus Documented sales performance (top 10% or Presidents Club) Proven track record of exceeding sales objectives Following experience a plus: MilitaryExperience during collegeWork/internshipCompetitive sportLeadershipHave a valid driver’s license and be insurable 25% travel may be required May need to work evenings and weekends as needed (conferences, programs) Requirements: Entrepreneurial spirit and driveDemonstrated business acumenDemonstrated analytical skillsDemonstrated success in persuasion, influence, and negotiation skillsDemonstrated leadership abilityDemonstrated ability to apply technical/scientific knowledgeFlexibility to learn new products over timeKnowledge of and experience with the selling processInitiative and execution-orientedTeamwork#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 80,000-85,000 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 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.

Job Responsibilities: Serve as Single Point of Contact (SPOC) in assigned studies for investigative sites, RSU Team Lead, Clinical Operations, Feasibility, Site Identification, Project Leadership and GICS. Ensure adherence to standard operating procedures (SOPs), work instructions (WIs), quality of designated deliverables and to project timelines. Where applicable, act as a Country Lead for projects with no regional Lead assigned. Perform Regulatory, Start-up and Maintenance activities according to applicable regulations, SOPs and work instructions. Prepare site regulatory documents, reviewing for completeness and accuracy. Review, prepare and negotiate site contracts and budgets with sites, if applicable. Ensure accurate completion and maintenance of internal systems, databases and tracking tools with project specific information. Ensure contracts are fully executed, regulatory documents and approvals are granted, IP Release authorized and specific project deliverables are completed. Review and provide feedback to management on site performance metrics. Review, establish and agree on project planning and project timelines. Ensure overall project efficiency and adherence to project timelines. Ensure monitoring measures are in place and implement contingency plan as needed. May contribute to the collection, interpretation, analysis and dissemination of accurate regulatory intelligence to support assigned studies and wider company, as required. May assist in pre-award activities including bid defenses, proposals and oversights of the scope of work at country level. May provide input into contract and budget template development. May support importation activities. May have direct contact with sponsors on specific initiatives. May act as Local Regulatory, Ethics and Contract Expert and reviewer of ICF. May act as mentor, and prepare and deliver country-specific training, for less experienced staff. May participate in feasibility and/or site identification activities. May perform Site Selection Visits if a trained monitor.   Job Requirements: Bachelor’s Degree in life sciences or a related field and 3 years’ clinical research or other relevant experience; or equivalent combination of education, training and experience. In-depth knowledge of clinical systems, procedures, and corporate standards. Good negotiating and communication skills with ability to challenge, if applicable. Effective communication, organizational, and interpersonal skills. Ability to work independently and to effectively prioritize tasks. Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines. Knowledge of applicable regulatory requirements, including local regulations, , SOPs and company’s Corporate Standards. Understanding of regulated clinical trial environment and knowledge of drug development process. 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.

*Home-based position - To be eligible for this position, you must reside in the same country where the job is located. Position Specifics This sponsor-dedicated role provides country-level oversight of clinical trials from study start-up through database lock and closeout. Operating in a fast-paced environment with evolving priorities, the role ensures high-quality data delivery and regulatory compliance across all phases of the trial. Candidates who will thrive in this role have expertise in drafting and managing informed consent process, managing site selection, patient recruitment strategies, and monitoring visit reports, while driving risk-based mitigation plans to proactively address study challenges. The position collaborates closely with cross-functional teams to support trial execution, maintain inspection readiness, and uphold GCP, SOP, and local regulatory standards. Two years of clinical trial management experience is required within a role that is accountable for driving and owning local trial activites at the regional level. Additional InformationAssociate Clinical Project Managers (aCPM)/Local Trial Managers are an integral part of clinical trial delivery, liaising with clinical teams to improve patients’ lives by bringing new drugs to the market faster. The aCPM is a member of the core project team responsible for project delivery of clinical studies to meet contractual requirements in accordance with SOPs, policies and practices. Clinical Project Management is focused on project delivery, productivity and quality resulting in strong financial performance and customer satisfaction. The aCPM supports the efforts of CPM to drive operational excellence and strategic leadership with our customers. Essential Functions Provide input in to the development of integrated study management plans with the core project team and/or sub-team. Accountable for assigned portion of clinical studies as per the contract while optimizing speed, quality and cost of delivery and ensuring consistent use of study tools and training materials and compliance with standard processes, policies and procedures. Set objectives of project sub-team(s), according to agreed upon contract, strategy and approach, effectively communicate and assess performance. Collaborate with other functional groups within the company where necessary to support milestone achievement and to manage study issues and obstacles. Monitor progress against contract and prepare/present project and/or sub-team information proactively to internal stakeholders. Support the project leader to prepare/present project and/or sub-team information proactively to external stakeholders. Identify risk (positive and negative) and contingencies and partner with project leader in problem solving and resolution efforts. Achieve project quality by identifying quality risks and issues, responding to issues raised by project sub-team members and partner with project leader planning/implementing appropriate corrective and preventative action plans. May serve as primary (for small projects) or back-up project contact with customer. Lead the efforts of a project sub-team, responsible for managing cross-collaboration of the sub-team to support milestone achievement and to manage issues and obstacles. Support the project leader in ensuring the financial success of the project. Forecast and identify opportunities to accelerate activities to bring revenue forward in partnership with the senior project leader. Identify changes in scope and partner with project leader to manage change control process as necessary. Identify lessons learned and implement best practices. May be assigned as the primary contact for vendors leading project vendor management and vendor management related activities as per project requirements. Qualifications Bachelor's Degree In life sciences or related field required 2 years clinical trial management experience Requires intermediate level knowledge of principles, theories, and concepts of a job area, typically obtained through advanced education combined with experience Knowledge of clinical trials - Knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements i.e. ICH GCP and relevant local laws, regulations and guidelines, towards clinical trial conduct. Broad protocol knowledge, therapeutic knowledge desired.; Communication - Strong written and verbal communication skills including good command of English language. Strong presentation skills. Problem solving - Strong problem solving skills. Organization - Planning, time management and prioritization skills. Ability to organize resources needed to accomplish tasks, set objectives and provide clear direction to others, experience planning activities in advance and taking account of possible changing circumstances. Prioritization - Ability to handle conflicting priorities. Quality - Attention to detail and accuracy in work. Results-oriented approach to work towards delivery and output. IT Skills - Good software and computer skills, including MS 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. Strong customer service skills. Cross-collaboration - Ability to work across geographies displaying high awareness and understanding of cultural differences. Finances - Good understanding of project financials. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role, when annualized, is $68,400.00 - $232,800.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Présentation de l'entreprise A la croisée de deux univers, la santé et les nouvelles technologies, IQVIA est l’expert des données de santé depuis plus de 60 ans et dans 140 pays. IQVIA s’appuie sur ses bases de données uniques, sur son expertise et sur ses outils d’analyse pour apporter des services et des solutions de conseil aux acteurs du système de santé. Grace à l’utilisation de méthodes innovantes telles que l’intelligence artificielle, IQVIA contribue à l’amélioration de la prise en charge des patients et au développement de la médecine de demain. Nous participons à la mise en place d'un système de santé plus moderne, plus efficace et plus adapté aux besoins de chacun. IQVIA fournit des solutions concrètes grâce à son savoir-faire : • Une expertise en santé : connaissances institutionnelles et expertise du domaine à travers les maladies, les géographies et les méthodes scientifiques • Une capacité analytique avancée pour une prise de décision plus rapide et plus précise générée par des analyses avancées conçues pour les soins de santé • Des données inégalées. IQVIA possède l'une des plus grandes sources de données de soins de santé au monde avec des protections de confidentialité innovantes • Une technologie transformative. Des technologies de pointe pour fournir un accès en temps réel aux informations critiques sur les opérations Contexte Le département Data & Tech d’IQVIA France recrute un Data Engineer pour rejoindre son équipe Research & Innovation. Cette équipe développe des preuves de concept (PoC), de nouveaux produits et des améliorations de solutions existantes afin de soutenir les activités d’IQVIA. Ses réalisations couvrent un large éventail de livrables, notamment : des modèles standards utilisés par les équipes de conseil (modèles de projection, détection des promotions, élasticité-prix, etc.) ;des applications web à usage interne et externe ;des pipelines de données traitant de grands volumes de données de vente (sell-out) ainsi que des données de santé sensibles.L’équipe constitue également une référence technique au sein du bureau français, notamment sur les sujets d’architecture, de qualité logicielle et d’intégration des nouvelles technologies d’intelligence artificielle. À ce titre, elle est volontairement exposée à une grande diversité de sujets et d’activités afin de répondre à l’évolution des besoins des utilisateurs. Le Data Engineer travaillera en étroite collaboration avec le Technical Lead et contribuera aux projets de développement et d’innovation de l’équipe. Ce poste s’adresse à un Data Engineer de niveau intermédiaire à senior, disposant d’au moins 3 ans d’expérience professionnelle en développement logiciel dans des environnements fortement orientés données. Il s’agit principalement d’un rôle de contributeur individuel, avec la possibilité de prendre progressivement la responsabilité technique de projets. Le poste combine des activités de Software Engineering, Data Engineering et de contribution aux bonnes pratiques techniques, en collaboration étroite avec les équipes Data Science, Produit et Production. Le Data Engineer devra participer activement aux décisions techniques, collaborer étroitement avec les membres de l’équipe et prendre progressivement la responsabilité de composants tels que les API, les pipelines de données et les pratiques de déploiement. Son périmètre couvrira aussi bien des preuves de concept que des systèmes de production ayant un impact concret sur l’activité. Principales missionsDéveloppement logiciel et produitContribuer activement aux développements, notamment sur les pipelines de données, les services back-end et les API web.Concevoir, développer et maintenir des pipelines de données fiables et performants.Participer à la modélisation et à la structuration des données afin de garantir un traitement et une exploitation efficaces.Accompagner la transformation des prototypes et preuves de concept en solutions prêtes pour la production.Garantir la qualité des développements de l’équipe, notamment via les tests, les revues de code, les outils et la documentation.Innovation et veille technologiqueAssurer une veille sur les évolutions des technologies logicielles, data, cloud, des frameworks et des outils associés.Contribuer au développement et à l’évaluation de preuves de concept.Participer à la définition de la feuille de route technique de l’équipe.Contribuer à la communication technique au sein du département, y compris via d’éventuelles formations.Collaboration et supportCollaborer avec les équipes Produit, Panel, Production et Infrastructure afin de garantir des solutions techniques alignées avec les besoins métier.Participer au suivi de la production, à l’analyse des incidents et à l’amélioration continue des systèmes déployés.Contribuer à la rédaction de documentations et d’explications techniques destinées aux parties prenantes internes, y compris les publics non techniques.Compétences requisesDiplôme de niveau Master en informatique, génie logiciel, ingénierie des données ou domaine connexe.Solide expérience professionnelle en développement logiciel, idéalement dans des environnements fortement orientés données ou intelligence artificielle.Excellente maîtrise de Python et du développement back-end (API, services, pipelines de données).Bonne expérience des bases de données relationnelles et du langage SQL.Maîtrise de Git, de la conteneurisation (Docker) et des pratiques CI/CD.Bonne compréhension de l’architecture logicielle, des stratégies de test et des contraintes d’exploitation.Volonté d’intervenir sur des sujets de data engineering, de développement back-end et de déploiement, avec la capacité d’apprendre certains aspects en cours de poste.Maîtrise professionnelle du français et de l’anglais.Connaissance des méthodes de développement logiciel Agile.Compétences complémentaires appréciéesLes compétences suivantes ne sont pas obligatoires mais constitueraient un atout : Expérience des plateformes cloud et infrastructures data (Azure, Kubernetes, Databricks, PySpark, etc.).Expérience avec les outils d’orchestration de pipelines de données (ex. : Airflow).Expérience dans le déploiement de services conteneurisés ou l’administration d’environnements cloud simples.Expérience de l’intégration de modèles de machine learning ou d’IA générative dans des systèmes de production.Connaissances en protection des données, anonymisation et gestion de données de santé sensibles.Expérience en développement front-end (React).Connaissance du secteur de la santé en France.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 OverviewDuring project assignments, works closely with Principal/Engagement Manager, serving as a key contributor to client engagements, with a focus on client satisfaction and delivery quality.Considered to be a Subject Matter Expert (SME) within one or more specific functional or technical workstreams (e.g., Medicaid, Master Data Management, Chargebacks, Government Pricing, Testing, Managed Care Contracting, Commercial Contracting, Integration Development, Report Development, Historical Data Conversion, Direct / Indirect Sales, etc.) and demonstrates their knowledge and experience on both client engagements as well as on internal initiatives (trainings, development programs, industry updates and advancements, etc.) where their guidance and input is sought after. Leverages experience with the Software design lifecycle (SDLC) and revenue management software systems (Flex, Powered by N, Gross to Net) to advise clients on best practices within the life sciences industry and capable of navigating and troubleshooting application issues with little to no oversight. Often leads client-facing presentations, requirement gathering workshops, and prepares and conducts streamlined training sessions. May oversee one or more resources within a workstream, providing guidance and managing team deliverables along with successful completion of owned assignments. Responsibilities • Serves as primary owner of one or more project areas or workstreams, focusing on client satisfaction and delivery quality.• Leads workstreams / projects to ensure efficient and quality deliverables.• Serves as lead solutions-based expert applying consultative problem-solving skills.• On a small-to-mid scale project, acts as Overall Lead, or Functional/Technical Workstream Lead (e.g., Purchase Based Contracts, Utilization Based Contracts, Master Data Management, Integrations, Test Lead, etc.). • On a large-scale project, act as sub-Workstream Lead (e.g., Workstream Test Lead, Contract Modeling Lead, Cutover Lead).• Supports engagement timelines to ensure practice targets are achieved.• Provides advice and leadership to clients to deliver solutions and provide value.• Participates in proposal development and delivery.• Represents IQVIA positively through strong performance and professional interactions, including participation in Thought Leadership activities (expertise requests, conference attendance, writing blogs and white papers). • Manages one or more resources and provides guidance and support for junior team members during client engagements.• Provides mentorship for one or more junior resources outside of client engagements and provides valuable input to program leadership.Qualifications• Bachelor's Degree Req• Master's Degree (MBA) Pref, PMP certification a plus• 4-7 years of experience in the pharmaceutical/healthcare/life sciences or consulting industry• Expertise in at least one or more of (but not limited to) the following, along with knowledge of others in this list:• Medicaid• Master Data Management• Chargebacks• Government Pricing• Testing• Managed Care Contracting• Commercial Contracting• Integration Development• Report Development• Historical Data Conversion• Direct / Indirect Sales• Exemplary client-facing delivery skills with the ability to lead workshops, identify pain points, troubleshoot issues and determine solutions.• Has broad knowledge of the pharmaceutical/healthcare/life sciences industry• Works willingly and effectively with others in and across the organization to accomplish team goals.• Knowledge and understanding of one or more key workstreams within pricing and contracting.• Experience with revenue management software systems (Flex, Powered by N, Gross to Net) and best practices, related to one or more functional areas.• Demonstrates strategic thinking and advanced analytical skills.• Excellent interpersonal skills including valuing the opinions of others and encouraging of knowledge sharing.• Able to self-manage and prioritize tasks as well as oversee the deliverables of other team members. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is 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 $102,200.00 - $284,700.00. 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.

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.

Per conto di una importante realtà multinazionale chimico-farmaceutica, riconosciuta a livello internazionale per la sua lunga tradizione di innovazione e impegno nella ricerca, siamo alla ricerca di un/una Specialista in Informazione Scientifica Core Therapies. La figura selezionata avrà l’opportunità di entrare a far parte di un contesto dinamico e innovativo, contribuendo attivamente alla promozione di soluzioni terapeutiche all’avanguardia e al miglioramento della qualità della vita dei pazienti. Il profilo inserito, riportando direttamente al National Sales Manager Core Therapies di riferimento, sarà responsabile della divulgazione e comunicazione delle informazioni scientifiche sui farmaci della Società verso specialisti in Pneumologia, ai sensi del Dlgs 219/06. Si occuperà altresì di gestire e sviluppare relazioni strategiche con gli specialisti in Pneumologia e con i principali stakeholder sanitari. Il suo obiettivo sarà definire un’informazione medico scientifica verso gli operatori sanitari personalizzata ed omnicanale, al fine di promuovere i farmaci assegnati. ZONE DI LAVORO: Lazio-Sardegna; residenza preferibile: RomaRESPONSABILITA’: Presentare prodotti farmaceutici e aggiornare sui cambiamenti delle linee guida terapeutiche, agendo come punto di riferimento principale per un target definito di HCP (Health Care Professionals) in ambito pneumologico.Garantire una corretta informazione scientifica attraverso l’utilizzo dei mezzi messi a disposizione dalla Società e nel rispetto delle normative vigenti e delle procedure Aziendali.Sviluppare e implementare piani di engagement personalizzati basati su dati e insight.Utilizzare un approccio omnicanale (incontri in presenza, da remoto, eventi).Supportare le attività con team interni (marketing, medical, market access) per garantire un’informazione medico scientifica accurata ed aggiornata.Monitorare costantemente gli account per avere una visione a 360° (quote di mercato, attività recenti, risposte a campagne…).Fornire feedback strutturati al team analytics tramite la piattaforma CRM messa a disposizione delle Società.Partecipare attivamente allo scambio di insight tra ruoli sul campo e ruoli di sede secondo processi e modalità condivise.Costruire relazioni di valore con gli HCP, comprendendone profondamente i bisogni clinici e gli interessi scientifici in accordo con le funzioni Aziendali.Costruire relazioni con i Territory Manager per una gestione integrata del territorio e dei principali stakeholder.Monitorare le dinamiche del mercato respiratorio nella propria area.Mantenere un elevato livello di aggiornamento scientifico e normativo.Raccogliere tramite appositi moduli eventuali segnalazioni di eventi avversi, comunicandole prontamente alla Farmacovigilanza.REQUISITI: Laurea in discipline scientifiche (legge 219/06)Esperienza pregressa di almeno 3/4 anni nella medesima mansioneConoscenza ed introduzione con il target pneumologico del territorio assegnatoCapacità avanzate di interpretazione dei dati di mercato e identificazione di tendenze strategicheOttimo background scientificoCOMPLETANO IL PROFILO: Spiccate doti di comunicazione e di negoziazioneForte orientamento al risultatoAscolto attivo e capacità di lavorare in teamCapacità organizzative e gestionaliProblem solving e team workingConoscenza lingua inglese è da considerarsi un plusOFFRIAMO: CCNL: Industria Chimica e FarmaceuticaTipologia contrattuale: Tempo indeterminato – Staff Leasing con IQVIARange retributivo o Retribuzione Annua Lorda: 45.000 €/49.000 €Premi al raggiungimento degli obiettiviAuto aziendaleIl pacchetto retributivo sarà definito in base all’esperienza, alle competenze e ai criteri di equità interna. La crescita professionale e gli adeguamenti retributivi sono basati su criteri trasparenti e oggettivi. Ci impegniamo a garantire pratiche retributive eque e inclusive, in linea con le normative sulla trasparenza salariale (Direttiva UE 2023/970). Candidature SENZA i requisiti richiesti non saranno prese in piena considerazione. Si prega di inserire l'autorizzazione al trattamento dei dati personali ai sensi dell’art. 13 d. lgs. 30 giugno 2003 n°196 – “Codice in materia di protezione dei dati personali” e dell’art. 13 GDPR 679/16 – “Regolamento europeo sulla protezione dei dati personali” e autorizzazione alla cessione di tali dati alle aziende Clienti di IQVIA. La ricerca è di carattere urgente ed è rivolta ad entrambi i sessi (L.903/77). #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. The potential base pay range for this role is 45.000 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.