IQVIA

Software Engineer

• Conduct statistical programming work of clinical data using SAS Software
• Ensure programs, outputs, and documentation comply with ICH guidelines and company SOPs
• Generate analysis datasets according to CDISC standards and SAP
• Implement analysis methods according to SAP and produce summary tables, graphs, and data listings using SAS
• Conduct ad hoc analyses
• Validate programs and associated results produced by other programming colleagues
• Participate in TLF shell preparation and review
• Assist statistician with SAP preparation
• Run CDISC validation programs, such as OpenCDISC reports, to ensure ADaM datasets are CDISC compliant
• Learn and implement Incyte standard SAS macros for efficient clinical data analyses under Lead Programmer supervision
• Program individual studies independently with minimum supervision
• Check validation summary reports for errors, warnings, and proper SAS program documentation
• Review individual study CDISC validation output

Senior Statistical Programmer, Inflammation

Affiliate Manager

• Develop and deliver value-added commercialization strategies addressing complex Emerging Biopharma client needs
• Build trusted-partner status through commercial content expertise and thought leadership
• Conduct client strategy sessions outlining integrated commercial launch plans
• Check in regularly with clients to assess progress and address questions
• Leverage prioritization frameworks to focus pre-commercial team efforts on high-potential accounts
• Prepare analytical proof points and recommendations for launch-critical success factors
• Lead senior-level client meetings covering launch planning, market and therapy-area insights, and solution design
• Own client engagements and responsibility for client satisfaction and quality/value delivery
• Create and elevate new business opportunities through follow-on work and new revenue opportunities
• Mentor, coach, and share subject-matter expertise to develop individuals and capabilities

Asset Commercialization Partner – Emerging Biopharma

• Conduct statistical programming work of clinical data using SAS Software
• Ensure programs, outputs and documentation comply with ICH guidelines and company SOPs
• Generate analysis datasets according to CDISC standard and SAP
• Implement analysis methods according to SAP and produce summary tables, graphs and data listings using SAS
• Conduct ad hoc analyses
• Validate programs and associated results produced by other programming colleagues
• Participate in TLF shell preparation and review
• Assist statistician with SAP preparation
• Run CDISC validation programs such as OpenCDISC reports to ensure ADaM datasets are CDISC compliant
• Learn and implement Incyte standard SAS macros for efficient clinical-data analyses under Lead Programmer supervision
• Independently program for individual studies with minimum supervision
• Check validation summary reports for errors, warnings, and proper SAS-program documentation
• Review individual study CDISC validation output

Senior Statistical Programmer – Oncology

Sales Operations Manager

• Administer Sales Incentive Compensation plans for a portion of the US Go-To-Market teams
• Compile Incentive Compensation datasets from IQVIA revenue or CRM systems
• Apply crediting rules
• Upload credited datasets to Sales Performance Management software (Varicent)
• Review achievement and payout results with SIP participants and managers
• Manage exception requests
• Ensure eligible participants, such as new hires, are on sales incentive plans
• Participate in the annual Incentive Compensation Governance program, including plan development and target setting
• Support special sales programs and contests as needed

Sales Operations Analyst – Incentive Compensation

• Contribute to the development of German AMNOG dossiers, focusing on statistical analyses for Module 4
• Perform scientific assessment and analysis of clinical trial data, including efficacy, safety, patient-relevant endpoints, and subgroup analyses
• Perform meta-analyses and indirect treatment comparisons and support interpretation of statistical outputs
• Automate and standardize analysis workflows for efficiency, consistency, and reproducibility
• Collaborate with Market Access, HEOR, Medical Affairs, and EU-HTA teams
• Ensure scientific quality, clarity, and consistency of generated outcomes
• Monitor and interpret methodological developments from IQWiG, G-BA, and relevant HTA bodies

Programmer, SAS, R, German

Recruitment

• Coordinate operational execution of patient recruitment and retention deliverables for assigned clinical studies
• Coordinate translations, printing, and shipping of patient-facing and study materials across multiple countries
• Prepare and compile country-specific regulatory submission packages
• Maintain and track study timelines, milestones, and deliverables using Smartsheet or designated project management tools
• Support project-specific, interdepartmental, and role-specific training activities
• Maintain large volumes of study-related data and ensure accurate, timely data entry
• Support finance activities, including periodic project and financial report generation and review
• Upload, maintain, and quality-control study documentation within eTMF/Wingspan or designated systems
• Ensure recruitment deliverables are accurate, compliant, and delivered within agreed timelines
• Identify operational risks, data discrepancies, and delivery challenges; communicate issues and mitigation actions
• Perform additional duties assigned by management

Patient Recruitment Specialist

Principal

• Act as principal owner of client engagements from initial needs conversations through solution development and project delivery oversight
• Create and elevate new business opportunities with existing and new client organisations
• Present educational and go-to-market materials internally and externally
• Identify opportunities to sell integrated solutions, including P&MA strategy, HEOR/HTA support, PRO instrument advice, and RWE strategy
• Engage project teams in designing, developing, and delivering projects using IQVIA capabilities and solutions
• Establish delivery excellence and ensure accurate, high-quality work meeting or exceeding client expectations
• Foster collaboration and inclusivity among project teams
• Monitor industry, client, and competitive trends to anticipate business challenges
• Lead thought leadership and firm-building initiatives through speaking engagements, client meetings, and publications
• Mentor, coach, and share subject matter expertise
• Lead ad hoc workstreams on recruitment, training, and development
• Serve as development lead to 3–4 staff

Principal, Health Economics, Health Technology Assessment – Nordics

General

• Perform, manage and co-ordinate activities for assigned opportunities/projects
• Perform data mining and analysis, formulate recommendations, and present to internal and potentially external stakeholders
• Train and support new team members/junior staff
• Make recommendations for process improvements
• Deliver accurate and robust country, site, or enrollment strategies for future studies and business opportunities
• Support development of feasibility, site-list, and enrollment-strategy materials for customer bid defense meetings and internal customers
• Collaborate with key stakeholders and IQVIA project teams to resolve issues
• Research therapeutic areas using databases, scientific literature, the internet, and expert medical knowledge
• Lead planning meetings with internal stakeholders and present data-gathering and analysis results
• Undertake therapeutic training and keep abreast of clinical research developments
• Use planning tools and understand system features to accomplish accurate country, site, or enrollment strategies

Site Identification Lead

Compliance

• Manage Quality Events, Quality Issues, deviations, and related investigations with relevant stakeholders
• Act as Deviation Owner and support CAPA definition, implementation, tracking, effectiveness assessment, and closure
• Support internal and external audits, audit readiness activities, and remediation of audit findings
• Ensure quality records, supporting documentation, and evidence are complete, accurate, traceable, and inspection ready
• Support third-party governance and oversight from a quality and compliance perspective
• Contribute to third-party Quality Risk Assessments for GMA activities, including NIS, RWE/RWD activities, Research Collaborations, and partnerships
• Follow up on identified risks and mitigation actions
• Identify, assess, and escalate potential risks from third-party due diligence, qualification, and oversight activities
• Ensure compliance with SOPs, business guidance documents, quality standards, and regulatory requirements
• Support Research Collaboration and selected non-vendor third-party due diligence and assessment activities
• Coordinate with internal stakeholders and third parties to obtain due diligence and assessment documentation
• Maintain and continuously improve TPM due diligence tools, including TPIAT
• Lead or contribute as a subject matter expert to the design, revision, implementation, and improvement of GMA V&TPM quality, compliance, governance processes, standards, procedures, and guidance
• Provide V&TPM quality and compliance expertise, guidance, and training to operational teams and stakeholders
• Collaborate with ESP Quality Assurance, Medical QA, GMA Medical Governance & Risk Management, Procurement, VPG, and other stakeholders to ensure effective third-party oversight

Vendor & Third-Party Management Quality & Compliance Manager

Account Manager

• Work on priority accounts for the client to maintain and drive growth
• Maximise opportunities using successful negotiation skills
• Defend and grow specific accounts
• Collaborate with internal and external stakeholders
• Achieve targets autonomously in primary care
• Maintain full accountability for product sales

Virtual Key Account Manager

Manager

• Cover the South UK region as Regional Business Manager
• Provide a high quality commercial approach
• Maximise opportunities and investments using successful negotiation skills
• Produce and implement bespoke initiatives enabling access to the client's products by NHS and private providers
• Maintain a high degree of knowledge of defined therapy areas and NHS policies, both local and national
• Proactively review current positions and provide solutions to ensure use of the client's products

Regional Business Manager

French

• Participate in all required orientation, training, and calibration activities
• Review case data and prepare for rater discussions, ensuring all relevant documents and scale items are available
• Conduct live interactions with raters to provide feedback and guidance on assessment methodology and scoring
• Complete assigned tasks and rater interactions according to schedule
• Submit all required documentation accurately and on time
• Evaluate assessment quality and confirm standardized assessment practices
• Support rater performance through functional assessments, such as mock interviews
• Assist with communication materials and documentation as needed

Clinical Trial Independent Rater – French Speaking

Field Engineer

• Troubleshoot, repair, and update medical devices in hospitals throughout the United States
• Organize, test, install, and configure medical devices, hardware, software, and network products
• Set up and organize equipment and workstations
• Conduct routine checks and record product-test data after installation and configuration
• Manage project timelines and customer needs
• Travel nationally to support customer needs
• Work assignment-based schedules with typically 1–3 weeks onsite
• Provide 3 weeks of open availability per month

MedTech Field Service Technician, Entry Level

• Troubleshoot, repair, and update medical devices in hospitals throughout the United States
• Collaborate with healthcare professionals and on-site teams
• Organize, test, and update medical devices
• Install and configure hardware, software, and network products
• Set up and organize equipment and workstations
• Conduct routine checks and record data from product tests after installation and configuration
• Manage project timelines and customer needs
• Travel nationally to support customer needs
• Complete assignments typically requiring 1–3 weeks onsite

MedTech Field Service Software Tech, Entry Level

• Navigate hospital units and coordinate with unit nurses to assist with pulling pumps as needed
• Use clinical nursing expertise to answer questions and address concerns about medical devices
• Collect devices in hospital settings while collaborating with department nursing staff and field service technicians
• Facilitate room-to-room medical device upgrades
• Provide updates, reports, and feedback during and after in-service assignments
• Use hospital experience and customer service skills to ensure device collection does not interfere with facility activities
• Travel nationally to support customer needs
• Work independently in customer settings with minimal supervision