{"data":{"company":{"name":"IQVIA Laboratories","slug":"iqvia-laboratories","logo_url":"https://logos.yubhub.co/jobs.iqvia.com.png","canonical_domain":"jobs.iqvia.com","editorial":null,"wikidata_id":null,"founded":null,"ceo":null,"founders":[],"hq_location":null,"industry":null,"employee_count":null,"official_website":null,"wikipedia_url":null,"stock_ticker":null,"stock_price":null,"market_cap":null,"revenue":null,"ipo_date":null,"sector":null,"full_time_employees":null,"company_description":null,"twitter_username":null,"linkedin_id":null,"instagram_username":null,"facebook_id":null,"parent_org":null,"country":null,"github_org":null,"github_public_repos":null,"github_followers":null,"github_verified":0,"github_description":null,"github_location":null,"github_blog":null,"github_twitter":null,"stock_exchange":null,"stock_beta":null,"stock_range":null,"stock_is_actively_trading":null,"fmp_image":null,"fmp_address":null,"fmp_city":null,"fmp_state":null,"fmp_country":null,"recent_news":[],"search_interest_index":null,"search_interest_trend":null,"wikipedia_monthly_views":null,"hn_mention_count":null,"hn_top_stories":[],"wayback_first_year":null,"sec_incorporation_state":null,"sec_latest_filing_type":null,"sec_latest_filing_date":null,"sec_filings":[],"research_papers_count":null,"research_citations_count":null,"research_h_index":null,"research_topics":[],"is_federal_contractor":null,"earnings_calendar":[],"industry_canonical":null,"enrichment_sources":[],"last_enriched_at":null},"hiring":{"total_jobs":16,"categories":[{"category":"research","count":6},{"category":"healthcare","count":5},{"category":"operations","count":2},{"category":"it","count":1},{"category":"finance","count":1},{"category":"engineering","count":1}],"experience_levels":[{"level":"senior","count":11},{"level":"mid","count":2},{"level":"entry","count":2}],"work_arrangements":[{"arrangement":"onsite","count":5},{"arrangement":"hybrid","count":3}],"top_titles":[{"title":"Senior Scientist, Large Molecule Bioanalytical","count":2},{"title":"Unit Manager","count":1},{"title":"Specimen Management Associate 2","count":1},{"title":"Senior Scientist - Translational Science Lab, Flow Cytometry","count":1},{"title":"Scientist, Lab Operations","count":1},{"title":"Records Management Associate","count":1},{"title":"Purchasing Analyst 1","count":1},{"title":"Product Support Technical Advisor II","count":1},{"title":"Director, Test Code Product & Lifecycle","count":1},{"title":"Clinical Trial Material Manager (2nd Shift)","count":1},{"title":"Clinical Lab Scientist (CLS) – Automated Chemistry","count":1},{"title":"Associate Principal Scientist, Large Molecule Bioanalytical","count":1},{"title":"Associate Manager","count":1},{"title":"Associate BioServices Study Lead - Hybrid","count":1},{"title":"Associate BioServices Study Lead","count":1}],"locations":[{"location":"valencia, ca","count":3},{"location":"indiana","count":3},{"location":"marietta, ga","count":2},{"location":"livingston, west lothian","count":2},{"location":"indianapolis, in","count":2},{"location":"portishead","count":1},{"location":"ithaca, ny","count":1},{"location":"indianapolis, indiana","count":1},{"location":"bratislava","count":1}],"skills":[{"skill":"Mass Spectrometry","required":4,"preferred":1,"total":5},{"skill":"Microsoft Excel","required":3,"preferred":0,"total":3},{"skill":"PowerPoint","required":3,"preferred":0,"total":3},{"skill":"Data Analysis","required":3,"preferred":0,"total":3},{"skill":"Laboratory Instrumentation","required":2,"preferred":0,"total":2},{"skill":"Ce-sds","required":1,"preferred":1,"total":2},{"skill":"Sds-page","required":1,"preferred":1,"total":2},{"skill":"BCA","required":1,"preferred":1,"total":2},{"skill":"Sec-hplc","required":1,"preferred":1,"total":2},{"skill":"UV-visible Spectroscopy","required":1,"preferred":1,"total":2},{"skill":"Word","required":2,"preferred":0,"total":2},{"skill":"LIMS","required":2,"preferred":0,"total":2},{"skill":"Communication","required":1,"preferred":1,"total":2},{"skill":"Liquid Chromatography","required":2,"preferred":0,"total":2},{"skill":"Immunoassay Techniques","required":2,"preferred":0,"total":2},{"skill":"Sample Extraction","required":2,"preferred":0,"total":2},{"skill":"Assay Method Development","required":2,"preferred":0,"total":2},{"skill":"Good Laboratory Practices","required":1,"preferred":0,"total":1},{"skill":"Microsoft Office Suite","required":1,"preferred":0,"total":1},{"skill":"Scientific Protocols","required":1,"preferred":0,"total":1}],"salary_stats":{"count":13,"min":23600,"q1":71200,"median":98900,"q3":99850,"max":203950},"job_types":[{"type":"full-time","count":14},{"type":"contract","count":1}],"latest_jobs":[{"id":"job_e264e2c8-33e","title":"Senior Scientist - Translational Science Lab, Flow Cytometry","source_url":"https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Valencia-CA-United-States-of-America/Senior-Scientist---Translational-Science-Lab--Flow-_R1552924","location":"Valencia, CA","job_type":"full-time","experience_level":"senior","work_arrangement":null,"category":"Research","description":"<p>We are seeking a Senior Scientist - Translational Science Lab, Flow Cytometry to join IQVIA Laboratories. As a Senior Scientist, you will be responsible for developing and optimizing moderately complex assays and methods to support timely and effective laboratory delivery.</p>\n<p><strong>Job Summary:</strong> The Senior Scientist - Translational Science Lab, Flow Cytometry is responsible for developing and optimizing moderately complex assays and methods to support timely and effective laboratory delivery. This role also provides technical leadership across troubleshooting, method transfer, and cross-functional collaboration to support scalable laboratory operations.</p>\n<p><strong>Responsibilities:</strong></p>\n<ul>\n<li>Plan assay and method development activities and draft clear, robust laboratory methods</li>\n<li>Execute method development experiments and support validation and analytical testing activities as needed</li>\n<li>Troubleshoot assays and apply root cause analysis to optimize performance and resolve technical issues</li>\n<li>Transfer methods into validation processes and collaborate across functions to ensure methods are sustainable and scalable</li>\n<li>Lead low to moderately complex technical projects and guide assigned team members to achieve project deliverables</li>\n<li>Mentor and train junior staff while contributing technical expertise to scientific reports, presentations, and documentation</li>\n<li>Support laboratory equipment maintenance, operational standards, and evaluation of new instrumentation</li>\n</ul>\n<p><strong>Requirements:</strong></p>\n<ul>\n<li>Bachelor&#39;s degree in a relevant scientific discipline is required</li>\n<li>4 years of related experience in method or assay development or specific methodology area</li>\n<li>2 years&#39; experience working with flow cytometry</li>\n<li>Familiarity and working knowledge of immunology</li>\n<li>Sound knowledge of assay/method development and scientific principles, theories, concepts, and state of the art instrumentation</li>\n<li>Experience with method validation, assay troubleshooting, and transfer of methods into laboratory operations</li>\n</ul>\n<p><strong>Preferred Skills:</strong></p>\n<ul>\n<li>Strong troubleshooting and advanced problem-solving skills, including application of root cause analysis</li>\n<li>Effective communication and presentation skills with the ability to work successfully across functions, and comfortable training others</li>\n<li>Strong organizational skills and close attention to detail in a regulated laboratory environment</li>\n<li>Ability to manage multiple tasks independently and bring projects to completion within timeline expectations</li>\n<li>Ability to establish and maintain effective working relationships with coworkers, managers, and clients</li>\n</ul>\n<p><strong>What We Offer:</strong> We put our employees at the center of everything we do and are committed to providing them, and their families, with benefits that meet their diverse and changing needs. We invest in integrated benefits programs and resources to take care of our employees&#39; physical, mental and emotional, financial and social well-being so they can thrive at home and at work, at any stage of their well-being journey.</p>\n<p>The potential base pay range for this role, when annualized, is $64,200.00 - $133,600.00.</p>","enriched_at":1793322991719},{"id":"job_9b6b65ab-14e","title":"Director, Test Code Product & Lifecycle","source_url":"https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Valencia-CA-United-States-of-America/Director--Test-Code-Product---Lifecycle_R1557879","location":"Valencia, CA","job_type":"full-time","experience_level":"senior","work_arrangement":null,"category":"Engineering","description":"<p>We are seeking a Director, Test Code Product &amp; Lifecycle to join IQVIA Laboratories. Provide technical leadership and management direction for database administration teams in a matrix-managed environment. Lead advanced database design, analysis, administration and performance optimization to support complex processing needs and future business requirements.</p>\n<p><strong>Responsibilities:</strong></p>\n<ul>\n<li>Provide technical leadership and management direction to database administration team members</li>\n<li>Manage resource allocations within a matrix-managed environment</li>\n<li>Lead, plan and oversee state-of-the-art database designs to solve complex database processing problems</li>\n<li>Perform complex database analysis and database design tasks using advanced techniques on the forefront of technology</li>\n<li>Ensure databases meet required operational standards and performance levels, including reliability, response time and query execution time</li>\n<li>Prepare cost analyses and justification for difficult database systems</li>\n<li>Serve as a senior consultant to staff by providing strategic technical advice and consultation on database analysis and design reviews</li>\n<li>Participate in the administration, monitoring, tuning and support of databases in the production environment</li>\n</ul>\n<p><strong>Requirements:</strong></p>\n<ul>\n<li>Bachelor&#39;s Degree Computer Science, a related field, or equivalent experience</li>\n<li>Twelve (12) years of information technology experience</li>\n<li>Eight (8) years experience in the database administration area</li>\n<li>Experience in clinical or regulated laboratory environments is helpful</li>\n<li>Experience applying database design approaches that consider existing and future needs, capacity, limitations, operating time and desired results</li>\n<li>Experience evaluating database implementation approaches, backup strategies and recovery strategies</li>\n<li>Knowledge of database administration activities including denormalization, data archival schemes, sizing, data definition language and database objects</li>\n<li>Knowledge of referential integrity, security enforcement and application optimization</li>\n</ul>\n<p><strong>Benefits:</strong> We put our employees at the center of everything we do and are committed to providing them, and their families, with benefits that meet their diverse and changing needs. We invest in integrated benefits programs and resources to take care of our employees&#39; physical, mental and emotional, financial and social well-being so they can thrive at home and at work, at any stage of their well-being journey.</p>\n<p>The potential base pay range for this role, when annualized, is $107,800.00 - $300,100.00.</p>","enriched_at":1793308149888},{"id":"job_a5525a64-d01","title":"Unit Manager","source_url":"https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Portishead-United-Kingdom/Associate-Group-Leader---In-Vivo-Unit-Manager_R1567765","location":"Portishead","job_type":"full-time","experience_level":"senior","work_arrangement":"onsite","category":"Research","description":"<p>We are seeking a compassionate and proven Unit Manager to lead and manage an in vivo facility at our Discovery Sciences site in Portishead.</p>\n<p>You will be responsible for the smooth operation of the animal unit, ensuring compliance with UK Home Office regulations, and resolving day-to-day leadership tasks. You will also manage several Technical and Husbandry Specialists, while maintaining the highest standards of animal welfare, staff performance, and procedural compliance.</p>\n<p><strong>Main Tasks</strong></p>\n<ul>\n<li>Operational:</li>\n</ul>\n<p>+ Provide operational and people management for a small rodent animal unit   + Ensure compliance with the Animals (Scientific Procedures) Act 1986 (ASPA) and all Home Office, institutional, and ethical requirements   + Act as a holder of a Home Office Personal Licence (PIL) and perform licensed procedures as required   + Oversee animal welfare, husbandry standards, health monitoring, and environmental conditions within the facility   + Support staff training, performance management, and rota planning   + Maintain accurate records relating to animal use, staffing, training, and compliance   + Liaise with scientists, veterinarians, the NACWO, and other Named Persons to support study delivery   + Contribute to continuous improvement of facility processes, SOPs, and regulatory readiness   + Support internal and external audits and inspections   + Keep up to date on latest initiatives concerning animal welfare   + Liaise with external sites, facilities to aid continuous improvement in animal welfare</p>\n<ul>\n<li>People Leader:</li>\n</ul>\n<p>+ Effectively manage direct reports on a day-to-day basis   + Establish strong working relationships across the management community   + Identify areas for improvement and development, and facilitate opportunities for self and direct reports   + Be a positive influence across the group, able to coach, guide, and mentor more junior staff and peers as needed</p>\n<p><strong>Qualifications &amp; Experience</strong></p>\n<ul>\n<li>Degree, HND, or equivalent qualification in a biological or life sciences discipline, or significant equivalent experience in laboratory animal science</li>\n<li>Demonstrable lab-based industry-led experience in the Contract Research Organisation or biotech discovery environment</li>\n<li>Proven leadership or supervisory experience, overseeing smaller teams on a day-to-day basis</li>\n<li>Practical knowledge of standard conditions in animal facilities, including husbandry, biosecurity, environmental controls, and welfare assessment</li>\n<li>Strong communication skills, able to foster working relationships with peers and reports alike in a professional manner</li>\n<li>Home Office Personal Licence covering rodents</li>\n<li>Eligibility and willingness to be appointed as a NACWO under the Animals (Scientific Procedures) Act 1986 (ASPA), subject to Home Office approval</li>\n</ul>\n<p><strong>What We Offer You</strong></p>\n<ul>\n<li>Competitive benefits package starting from day one of employment, covering Financial &amp; Retirement, Health &amp; Wellness, Work-Life Balance, and Additional Perks</li>\n</ul>","enriched_at":1793306435883},{"id":"job_c7087af1-337","title":"Associate BioServices Study Lead - Hybrid","source_url":"https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Indianapolis-IN-United-States-of-America/Associate-BioServices-Study-Lead---Hybrid_R1564880","location":"Indianapolis, IN","job_type":null,"experience_level":"senior","work_arrangement":"hybrid","category":"Healthcare","description":"<p>We are seeking an Associate BioServices Study Lead - Hybrid to join IQVIA Laboratories. As an Associate BioServices Study Lead, you will provide scientific oversight throughout the lifecycle of bioanalytical projects while delivering exceptional service to internal and external customers.</p>\n<p>Responsibilities:</p>\n<ul>\n<li>Provide scientific oversight for method development, method validation, and sample analysis projects</li>\n<li>Serve as Principal Investigator for GLP studies</li>\n<li>Prepare validation and sample analysis plans, approve experimental designs, and review data for regulatory compliance and scientific quality</li>\n<li>Review validation and bioanalytical reports for completeness and address findings from Quality Control and Quality Assurance reviews</li>\n<li>Monitor assigned projects, communicate status updates, and escalate schedule risks to management</li>\n<li>Investigate failed runs, coordinate method troubleshooting, assemble technical resources, and document investigation findings</li>\n<li>Maintain communication with customers, resolve sample discrepancies, coordinate customer visits, and support quote preparation</li>\n<li>Ensure projects are archived in accordance with IQVIA SOPs and comply with applicable Good Clinical Practice and Good Laboratory Practice standards</li>\n</ul>\n<p>Requirements:</p>\n<ul>\n<li>Bachelor&#39;s Degree in a scientific field</li>\n<li>3 years of related experience in a GLP laboratory environment</li>\n<li>Understanding of liquid chromatography combined with mass spectrometry, or in vitro and immunoassay techniques</li>\n<li>Experience with sample extraction, routine laboratory procedures, assay method development, and assay validation</li>\n</ul>\n<p>The Knowledge, Skills and Abilities Needed for This Role:</p>\n<ul>\n<li>Ability to achieve results through effective collaboration with colleagues and cross-functional partners</li>\n<li>Excellent attention to detail, scientific judgment, and written and verbal communication skills</li>\n<li>Ability to interact effectively with internal and external clients while working to defined objectives and timelines</li>\n<li>Ability to establish and maintain effective working relationships with coworkers, managers, and clients</li>\n</ul>\n<p>What We Offer You:</p>\n<ul>\n<li>Competitive salary: $64,200.00 - $133,600.00 per year</li>\n<li>Comprehensive benefits program to support physical, mental and emotional, financial and social well-being</li>\n</ul>","enriched_at":1793267973253},{"id":"job_eea788a8-c17","title":"Clinical Trial Material Manager (2nd Shift)","source_url":"https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Marietta-Georgia-United-States-of-America/Clinical-Trial-Material-Manager--2nd-Shift-_R1552456","location":"Marietta, GA","job_type":"full-time","experience_level":"senior","work_arrangement":"onsite","category":"Operations","description":"<p>We are seeking a Clinical Trial Material Manager (2nd Shift) to join IQVIA Laboratories at Marietta, GA.</p>\n<p>The Clinical Trial Material Manager leads daily second-shift (2:00 PM to 11:00 PM) manufacturing operations in a regulated, high-volume production environment. This role ensures on-time delivery, quality compliance, staff performance, and continuous improvement while partnering across Project Services, Warehouse, Logistics, Quality, and IT.</p>\n<p><strong>Responsibilities</strong></p>\n<ul>\n<li>Lead, coach, and develop a team of direct reports in a dynamic production environment</li>\n<li>Manage daily and long-range production schedules to meet customer demand and service-level production targets</li>\n<li>Prioritize urgent, same-day, and future-dated work orders to ensure on-time delivery</li>\n<li>Coordinate daily with Project Management, Warehouse, Logistics, Quality, and IT to resolve production issues and prevent delays</li>\n<li>Utilize LIMS to support production files, platform reports, production metrics, dashboards, and compliance reporting</li>\n<li>Perform root cause investigations for quality incidents, customer complaints, operations incidents, and in-process deviations</li>\n<li>Lead and support Lean, Six Sigma, and process improvement initiatives to optimize production flow and reduce bottlenecks</li>\n</ul>\n<p><strong>Requirements</strong></p>\n<ul>\n<li>Bachelor’s degree, 10 years of experience in lieu of degree</li>\n<li>Minimum 5 years of people management experience, managing 20 employees in a manufacturing environment</li>\n<li>Minimum 5 years of experience managing manual assembly or production lines</li>\n<li>Minimum 2 years of experience leading process improvement projects</li>\n<li>Working knowledge of Microsoft Excel, Outlook, and PowerPoint</li>\n<li>Working knowledge of ICH, GMP, and OSHA regulations</li>\n<li>Six Sigma Yellow or Green Belt experience required; certification preferred</li>\n</ul>\n<p><strong>Knowledge, Skills and Abilities</strong></p>\n<ul>\n<li>Strong leadership, coaching, and staff development skills in a high-volume production environment</li>\n<li>Ability to prioritize urgent and business-critical work while maintaining quality and compliance expectations</li>\n<li>Effective cross-functional communication skills with the ability to escalate risks, constraints, and operational performance updates</li>\n<li>Strong problem-solving skills with the ability to conduct investigations and drive root cause analysis</li>\n<li>Ability to support overtime, weekends, and holidays based on critical business needs and accelerated trial timelines</li>\n</ul>\n<p><strong>What We Offer</strong></p>\n<ul>\n<li>Competitive salary: $77,700.00 - $161,800.00 per year</li>\n<li>Comprehensive benefits program, including physical, mental and emotional, financial and social well-being resources</li>\n</ul>","enriched_at":1793161159190},{"id":"job_8ab3b4a6-79b","title":"Product Support Technical Advisor II","source_url":"https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Marietta-Georgia-United-States-of-America/Product-Support-Technical-Advisor-II_R1550660","location":"Marietta, GA","job_type":"full-time","experience_level":"senior","work_arrangement":"hybrid","category":"IT","description":"<p>We are seeking a Product Support Technical Advisor II to join IQVIA Laboratories at Marietta, GA (hybrid).</p>\n<p>Provide senior Tier-3 product support for enterprise laboratory applications and integrated systems supporting U.S.-based lab operations. This role drives rapid resolution of high-impact production incidents, delivers onsite technical troubleshooting, and helps maintain continuity across critical workflows such as kit production, sample processing, and study execution.</p>\n<p><strong>Responsibilities</strong></p>\n<ul>\n<li>Provide advanced Tier 2 and Tier 3 support for LTMS and associated integrated laboratory systems.</li>\n<li>Investigate and resolve complex application, workflow, data, and integration-related issues.</li>\n<li>Serve as the escalation point for support teams handling critical production incidents.</li>\n<li>Support business-critical laboratory operations while minimizing disruption to study execution and client deliverables.</li>\n<li>Collaborate closely with Product, Development, Infrastructure, Cloud, Quality, and Operations teams to drive issue resolution.</li>\n</ul>\n<p><strong>Requirements</strong></p>\n<ul>\n<li>Bachelor&#39;s Degree in Computer Science, Information Systems, Healthcare Technology, Life Sciences, or related discipline, or equivalent combination of education and experience.</li>\n<li>5+ years of experience supporting enterprise business applications in a production environment.</li>\n<li>Experience investigating and resolving complex application issues.</li>\n<li>Experience working with SQL for data analysis and troubleshooting.</li>\n<li>Experience supporting integrated enterprise applications and business workflows.</li>\n<li>Experience with ServiceNow or comparable IT Service Management platforms.</li>\n<li>Experience supporting production environments with defined SLAs and support processes.</li>\n<li>Create and maintain support documentation, runbooks, knowledge articles, and troubleshooting guides.</li>\n<li>Contribute to onboarding and training materials for support personnel.</li>\n<li>Participate in automation, monitoring, AI-assisted support, and operational improvement initiatives.</li>\n<li>Manage incident queues utilizing ServiceNow and supporting tools.</li>\n<li>Ensure adherence to service level agreements (SLAs) and support metrics.</li>\n<li>Participate in ticket triage, prioritization, escalation management, and queue governance activities.</li>\n<li>Perform detailed troubleshooting and root cause analysis of production issues.</li>\n<li>Analyze application logs, SQL data, integrations, workflows, and business transactions to determine root cause.</li>\n<li>Drive corrective and preventive actions for recurring issues.</li>\n<li>Participate in Problem Management and post-incident reviews.</li>\n<li>Identify opportunities to improve system stability, monitoring, and support processes.</li>\n</ul>\n<p><strong>Preferred Qualifications</strong></p>\n<ul>\n<li>Experience supporting clinical trial, healthcare, pharmaceutical, laboratory, or life sciences applications.</li>\n<li>Experience supporting Laboratory Information Management Systems (LIMS), Laboratory Trial Management Systems (LTMS), or other regulated operational platforms.</li>\n<li>Familiarity with cloud-based application architectures and Azure-hosted environments.</li>\n<li>Experience supporting data integrations, APIs, and enterprise workflow platforms.</li>\n<li>Understanding of clinical trial operations and laboratory business processes.</li>\n<li>Experience with ITIL processes and operational service management.</li>\n</ul>\n<p><strong>What We Offer</strong></p>\n<p>We put our employees at the center of everything we do and are committed to providing them, and their families, with benefits that meet their diverse and changing needs. We invest in integrated benefits programs and resources to take care of our employees&#39; physical, mental and emotional, financial and social well-being so they can thrive at home and at work, at any stage of their well-being journey.</p>\n<p>The potential base pay range for this role, when annualized, is $57,000.00 - $142,700.00.</p>","enriched_at":1793154626316},{"id":"job_32b196af-281","title":"Associate Manager","source_url":"https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Livingston-West-Lothian-United-Kingdom/Associate-Manager---1-x-Immunology-and-1-x-Biochem_R1539272","location":"Livingston, West Lothian","job_type":"full-time","experience_level":"senior","work_arrangement":null,"category":"Healthcare","description":"<p>We are seeking an Associate Manager to join our team at IQVIA Laboratories, a comprehensive global central laboratory services provider supporting clinical trials worldwide.</p>\n<p>As an Associate Manager, you will be responsible for supervising a team of lab staff and ensuring effective operational delivery. Your duties will include:</p>\n<ul>\n<li>Setting day-to-day operational activities for the team with a focus on daily delivery</li>\n<li>Hiring, training, and performance management of staff under the mentorship of management</li>\n<li>Supervising daily activities of assigned laboratory work groups through delegation, technical skills training, and work supervision</li>\n<li>Ensuring activity in the team meets safety guidelines and driving individual accountability for safety</li>\n<li>Reviewing laboratory metrics to identify initiatives and establishing additional metrics such as cost savings</li>\n<li>Ensuring policies, practices, and procedures are understood and followed by direct reports, customers, and stakeholders</li>\n<li>Assisting in the establishment and revision of laboratory policies and procedures</li>\n</ul>\n<p>Requirements:</p>\n<ul>\n<li>Bachelor&#39;s degree in a human biology-based science</li>\n<li>4 years of relevant experience in a clinical laboratory or clinical trials environment (biochemistry-based)</li>\n<li>Experience in technical leadership and cross-functional collaboration</li>\n<li>Proficiency with LIMS and other laboratory data systems</li>\n<li>Familiarity with CAPA processes and quality systems</li>\n<li>Ability to analyze and interpret complex data</li>\n<li>Ability to effectively coordinate and execute multiple tasks or projects simultaneously</li>\n<li>Ability to effectively write scientific and technical documents</li>\n<li>Understanding of LEAN 6 Sigma principles</li>\n</ul>\n<p>Benefits of joining IQVIA:</p>\n<ul>\n<li>Global exposure</li>\n<li>Variety of therapeutic areas</li>\n<li>Collaborative and supportive team environment</li>\n<li>Access to cutting-edge and innovative in-house technology</li>\n<li>Excellent career development and progression opportunities</li>\n<li>Work-life balance with a strong focus on positive well-being</li>\n</ul>","enriched_at":1793148557097},{"id":"job_1e34a5e6-9bd","title":"Purchasing Analyst 1","source_url":"https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Bratislava-Slovakia/Purchasing-Analyst-1_R1542317","location":"Bratislava","job_type":"full-time","experience_level":"entry","work_arrangement":null,"category":"Finance","description":"<p>IQVIA Laboratories is a global leader in drug discovery and development laboratory services. As a Purchasing Analyst 1, you will play a key part in advancing Procure to Pay (P2P) purchasing processes and supporting acquisition integrations.</p>\n<p><strong>Main Responsibilities:</strong></p>\n<ul>\n<li>Guide internal stakeholders on policy and practices for using procurement systems, raising requisitions, committing Purchase Orders to suppliers, and paying supplier invoices.</li>\n<li>Review requisitions for external vendor spend, check for accuracy, and process as appropriate.</li>\n<li>Ensure all Purchase Orders are dispatched to suppliers on a timely basis and follow-up as required to ensure they have been received, processed, and have a delivery date.</li>\n<li>Work with suppliers to amend delivery dates on goods and services as deemed necessary by the business.</li>\n<li>Ensure purchase orders comply with contract terms and work to improve the efficiency of the purchase to pay process.</li>\n<li>Ensure Purchase orders pricing is accurate, and take steps internally and with suppliers to correct price deviations in advance of invoice holds.</li>\n<li>Proactively manage supplier performance on PO commitments, delivery, and Invoice accuracy.</li>\n<li>Ensure suppliers follow the correct procedures for submitting invoices for payment.</li>\n<li>Supplier pricing negotiation.</li>\n<li>Supporting supplier performance &amp; relationship management.</li>\n<li>Work with Accounts Payable organizations to clear any invoices on-hold (matching exceptions) to ensure on-time supplier payments.</li>\n<li>Be the Subject Matter Expert for our Procurement Systems (Peoplesoft, Oracle, Coupa). Troubleshoot issues to resolution.</li>\n<li>Use system reporting and bespoke analysis in Excel and/or Power BI to drive decision making and prioritization.</li>\n<li>Extract spend data from accounts payable or other databases and create spend reports.</li>\n<li>Undertake RFP/RFQ work for competitively tendered business opportunities.</li>\n<li>Perform competitive analysis on supplier bids.</li>\n<li>Prepare and present regular and ad-hoc purchasing recommendations to purchasing management.</li>\n<li>Undertake Purchasing system UAT support activities as assigned.</li>\n<li>Perform other duties as assigned.</li>\n</ul>\n<p><strong>Essential Functions:</strong></p>\n<ul>\n<li>Extract and analyze spend data from Accounts Payable and other internal databases to develop accurate and actionable spend reports.</li>\n<li>Obtain and consolidate spend files from external vendors to establish baseline spend across key purchasing categories.</li>\n<li>Partner with functional stakeholders to gather requirements, define purchasing process steps, and establish project timelines.</li>\n<li>Benchmark and validate sourcing opportunities through Requests for Information (RFIs), develop and issue competitive Requests for Proposals (RFPs), and support negotiation of optimal commercial terms.</li>\n<li>Prepare and present purchasing recommendations, insights, and sourcing outcomes to purchasing management.</li>\n<li>Under guidance, collect and analyze IQVIA data from issue logs to support vendor performance reporting, and coordinate monthly and quarterly vendor management meetings.</li>\n<li>Ensure purchase orders align with contract terms and contribute to continuous improvement of the procure to pay (P2P) process.</li>\n<li>Perform additional duties and support special projects as assigned.</li>\n</ul>\n<p><strong>Qualifications:</strong></p>\n<ul>\n<li>Bachelor’s degree required; field of study in Business, Supply Chain, Finance, or related discipline preferred.</li>\n<li>Minimum 3 years of professional experience, including at least 1 year in purchasing, procurement, supply chain management, materials management, or a related function involving RFP processes; or an equivalent combination of education, training, and experience.</li>\n<li>Strong knowledge of purchasing methodologies, principles, processes, and best practices.</li>\n<li>Proficiency with Microsoft Office applications, particularly Excel for data analysis and reporting.</li>\n<li>Solid technical accounting understanding and ability to interpret financial data.</li>\n<li>Strong analytical and numeracy skills, with the ability to extract insights from complex datasets.</li>\n<li>Ability to identify financial or process issues and support the development of mitigating actions.</li>\n<li>Demonstrated ability to prioritize, organize, and manage multiple workstreams to meet deadlines in a fast-paced environment.</li>\n<li>Strong interpersonal skills with the ability to build and maintain effective working relationships with colleagues, managers, vendors, and cross-functional partners.</li>\n<li>Experience with procurement systems (e.g., PeopleSoft, Coupa) is highly desirable.</li>\n<li>Familiarity with LEAN, automation, or process improvement initiatives is a plus.</li>\n</ul>","enriched_at":1793143815085},{"id":"job_8c70d6c1-e46","title":"Clinical Lab Scientist (CLS) – Automated Chemistry","source_url":"https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Valencia-CA-United-States-of-America/Clinical-Lab-Scientist--CLS----Automated-Chemistry_R1559548","location":"Valencia, CA","job_type":"full-time","experience_level":"mid","work_arrangement":"onsite","category":"Healthcare","description":"<p>We are seeking a Clinical Lab Scientist (CLS) – Automated Chemistry to join IQVIA Laboratories at Valencia, CA.</p>\n<p>As a Clinical Lab Scientist, you will provide professional and technical expertise to perform automated and manual clinical laboratory testing within the Automated Chemistry area, ensuring accurate and timely results that support clinical research and patient care.</p>\n<p><strong>Responsibilities:</strong></p>\n<ul>\n<li>Perform and report automated and manual clinical laboratory testing with minimal supervision</li>\n<li>Verify quality control results and release laboratory results in accordance with licensing and regulatory requirements</li>\n<li>Maintain laboratory inventory, prepare reagents, and ensure equipment and testing materials are available for daily operations</li>\n<li>Troubleshoot laboratory processes and communicate testing irregularities that may impact results</li>\n<li>Support assay validations, assay improvements, and implementation of new testing configurations</li>\n<li>Maintain compliance with CLIA, CAP, GCLP, safety, quality, and company procedures</li>\n<li>Participate in audits, inspections, continuing education, and training activities</li>\n<li>Support special projects and other laboratory responsibilities as assigned</li>\n</ul>\n<p><strong>Requirements:</strong></p>\n<ul>\n<li>Valid Clinical Laboratory Science (CLS) license required</li>\n<li>Bachelor&#39;s Degree required</li>\n<li>Up to 5 years of relevant experience in a regulated laboratory</li>\n<li>Working knowledge of Good Clinical Laboratory Practices (GCLP), CLIA requirements, and applicable regulatory standards</li>\n<li>Proficiency with complex laboratory testing procedures, laboratory instrumentation, and quality control processes</li>\n</ul>\n<p><strong>Knowledge, Skills and Abilities:</strong></p>\n<ul>\n<li>Strong technical knowledge of clinical laboratory procedures, troubleshooting techniques, and laboratory safety practices</li>\n<li>Effective organizational, communication, and interpersonal skills with the ability to manage multiple priorities</li>\n<li>Strong attention to detail and ability to establish productive working relationships with coworkers, managers, and clients</li>\n</ul>\n<p><strong>Physical Demands:</strong> Ability to lift up to 50 lbs, frequent standing and walking, occasional sitting, close eye work requirement (computer, typing, reading small prints).</p>\n<p><strong>What We Offer:</strong> We put our employees at the center of everything we do and are committed to providing them, and their families, with benefits that meet their diverse and changing needs. We invest in integrated benefits programs and resources to take care of our employees&#39; physical, mental and emotional, financial and social well-being so they can thrive at home and at work, at any stage of their well-being journey.</p>\n<p>The potential base pay range for this role, when annualized, is $46,200.00 - $96,200.00.</p>","enriched_at":1793137331603},{"id":"job_007955f8-da6","title":"Specimen Management Associate 2","source_url":"https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Indianapolis-IN-United-States-of-America/Specimen-Management-Associate-2--First-Shift-_R1572804","location":"Indianapolis, Indiana","job_type":"full-time","experience_level":"entry","work_arrangement":"onsite","category":"Healthcare","description":"<p>We are seeking a Specimen Management Associate 2 to join IQVIA Laboratories in Indianapolis, Indiana.</p>\n<p>The Specimen Management Associate 2 supports the accurate receipt, identification, storage, and shipment of clinical specimens. This role also guides entry-level staff on routine procedures and serves as a point of contact for basic troubleshooting and problem resolution.</p>\n<p><strong>Responsibilities:</strong></p>\n<ul>\n<li>Accession, sort, label, store, and prepare clinical specimens for testing or shipment</li>\n<li>Maintain freezers, specimen inventories, supplies, compounds, and control materials as assigned</li>\n<li>Identify errors and potential specimen-management issues, resolving routine problems or escalating them to senior staff</li>\n<li>Guide entry-level employees on department procedures and assist with onboarding new team members</li>\n<li>Respond to after-hours alarms and other job-critical situations as required</li>\n<li>Support laboratory safety, quality, and 6S requirements and initiatives</li>\n<li>Communicate clearly, accurately, and promptly with cross-functional stakeholders</li>\n<li>Perform work in accordance with company procedures and applicable regulatory requirements</li>\n</ul>\n<p><strong>Requirements:</strong></p>\n<ul>\n<li>A high school diploma or equivalent is required</li>\n<li>At certain CAP/CLIA laboratory locations, a bachelor&#39;s degree in chemistry, biology, or medical laboratory technology is required</li>\n<li>Six months of related experience is preferred</li>\n<li>Basic knowledge of internal systems and procedures, with the demonstrated ability to navigate and resolve routine challenges</li>\n<li>Working knowledge of specimen accessioning, shipment, storage, inventory maintenance, and problem-resolution procedures</li>\n<li>Basic computer skills</li>\n</ul>\n<p><strong>Benefits:</strong> We put our employees at the center of everything we do and are committed to providing them, and their families, with benefits that meet their diverse and changing needs. We invest in integrated benefits programs and resources to take care of our employees&#39; physical, mental and emotional, financial and social well-being so they can thrive at home and at work, at any stage of their well-being journey.</p>\n<p><strong>Salary:</strong> The potential base pay range for this role, when annualized, is $35,900.00 - $74,800.00.</p>","enriched_at":1793124918478}],"category_normalised":[{"category":"research","count":6},{"category":"healthcare","count":5},{"category":"operations","count":2},{"category":"it","count":1},{"category":"finance","count":1},{"category":"engineering","count":1}],"velocity":{"weeks":[{"week_start":"2026-10-19","count":2},{"week_start":"2026-10-26","count":14}],"trend":"stable","wow_pct":600},"momentum":{"recent_14d":16,"prior_14d":0,"growth_pct":0,"classification":"stable"},"salary_vs_industry":{"company_median":98900,"industry_median":null,"percentile":null,"sample_size":13,"by_region":[{"region":"United States","company_median":98900,"industry_median":null,"sample":8},{"region":"India","company_median":98900,"industry_median":null,"sample":4}],"transparency_pct":81,"industry_transparency_pct":0,"transparency_warning":false},"market_share":{"company_jobs":16,"industry_total":16,"share_pct":100,"rank":1,"peer_count":1},"ai_exposure":{"occupation_weighted_score":0.092,"skill_weighted_score":0,"top_exposed_titles":[],"top_exposed_skills":[]},"peer_set":[],"skills_lq":[],"geographic_shift":{"current":[{"region":"United States","count":8,"share_pct":50},{"region":"India","count":4,"share_pct":25},{"region":"Unknown","count":4,"share_pct":25}],"emerging":[{"region":"United States","recent_30d":8,"prior_30d":0,"growth_pct":100},{"region":"India","recent_30d":4,"prior_30d":0,"growth_pct":100},{"region":"Unknown","recent_30d":4,"prior_30d":0,"growth_pct":100}],"shrinking":[]},"seniority_anomalies":{"exec_recent_30d":1,"exec_prior_90d_avg":0,"exec_growth_pct":100,"notable_exec_hires":[{"title":"Director, Test Code Product & Lifecycle","location":"Valencia, CA","posted_at":"2026-10-29"}]},"posting_dynamics":{"median_days_open":null,"industry_median_days_open":null,"long_open_count":0,"closure_rate_pct":20}}}}