Jobs at IQVIA

Promote paediatric enteral feed products to hospital consultants, dietitians, and community dieticians across North London. Build relationships with key healthcare networks, drive portfolio uptake, support product launches, and improve patient outcomes. The role combines field and digital sales, business planning, negotiation, independent working, and collaborative account development in secondary care.

Leads biostatistical activities across oncology and other clinical development programs. Oversees statistical analysis plans, ADaM specifications, datasets, TLFs, analyses, timelines, regulatory submissions, and agency interactions. Provides protocol, randomization, sample size, and efficacy consultation; advises biotech clients; supports bid defenses; mentors global biostatistics staff; and contributes to departmental standards, training, presentations, and resource coordination.

Supports account management and business development teams by delivering data services to supplier customers. Gathers requirements, develops custom reports, fulfills requests, analyzes and validates data, ensures timely and accurate deliverables, answers supplier queries, and provides marketplace insights. The role also maintains internal communications and develops knowledge of pharmaceutical, retailer, and wholesaler markets.

Performs setup, SAS programming, refreshes, and peer review of Cluepoints centralized monitoring platforms for clinical studies. Supports monitoring strategy development by implementing quality tolerance limits, key risk indicators, data quality assessments, and visualizations. Reviews protocols, understands study data sources and transfer specifications, maintains platform documentation in the eTMF, interprets basic statistical outputs, and collaborates directly with sponsors and stakeholders.

Design, build, test and validate eCRF databases for clinical trials using Oracle InForm Central Designer or Veeva CDMS Studio. Produce annotated study books, develop test steps and QC forms, implement SOPs/CRF standards, support workflow/dynamic form design, liaise with study teams on scope and timelines, and apply regulatory and data management best practices to ensure quality deliverables.

Conduct site selection, initiation, monitoring, and close-out visits for clinical studies. Manage recruitment, regulatory submissions, enrollment, CRF completion, data queries, site documentation, and TMF/ISF compliance. Train and communicate with study sites, assess protocol and GCP adherence, resolve issues, document monitoring findings, and collaborate with study teams. Support recruitment planning and site financial management when applicable.

Define, set up and ingest external clinical data streams (labs, ECG, imaging, EHR, wearables, genomics). Plan set-up activities, create trial-specific Data Transfer Agreements, translate medical concepts into data mappings, perform UAT, implement transfers into the CDR, monitor data quality and resolve provider conformance issues while ensuring regulatory and data protection compliance.

Implements patient access strategies for new medicines, including budgetary notifications, healthcare system preparation, and indication pull-through. Engages healthcare stakeholders, supports pre-launch planning, develops customer materials using data and analytics, and collaborates with medical and marketing teams. Leads stakeholder groups, identifies commercial opportunities within local health economies, and manages projects to quality and timeline standards across South and South West England.

Lead business development and strategic growth for IQVIA clinical solutions across EMEA mid-size pharmaceutical accounts. Responsibilities include achieving sales targets, managing strategic accounts, developing sales plans, identifying cross-sell opportunities, navigating complex clinical solution sales, coordinating proposals and contracts, maintaining pipelines through CRM reporting, and mentoring junior sales staff. The role requires strong clinical development, regulatory, commercial, financial, negotiation, and executive relationship-building expertise.

Leads business development and account management for IQVIA Biotech across Europe. Sells and closes significant CRO service deals spanning Phase I–IV clinical solutions, develops strategic accounts, builds C-suite relationships, identifies new opportunities, expands existing clients, and coordinates internal expertise to deliver tailored solutions. Requires strong clinical sales, biotech market knowledge, solution-selling, hunting, relationship-building, and strategic execution experience.

Leads regulatory strategy engagements and real-world evidence programs supporting regulatory decision-making across the product lifecycle. Advises clients on EMA, FDA, MHRA, Health Canada, and PMDA expectations; shapes study designs, submission strategies, and regulatory pathways. Owns delivery quality, client relationships, proposals, business development, and follow-on opportunities. Provides intellectual leadership, mentors junior consultants, builds team capabilities, and contributes to regulatory intelligence and recruitment.

Drive commercial growth and biosimilar adoption across NHS accounts in London and the South East. Develop territory and account plans, increase market share, build relationships with NHS stakeholders, support tenders and market access initiatives, deliver scientific and commercial product discussions, and collaborate with Medical Affairs, Market Access, Marketing, and Supply Chain teams while maintaining CRM compliance.

Deliver consulting projects for investors evaluating biopharma and life sciences investments. Responsibilities include commercial due diligence, valuation, asset screening, growth strategy, primary and secondary research, quantitative and qualitative analysis, client deliverables, presentations, workstream leadership, proposal development, recruiting, training, and contributing to team intellectual property.

Manages end-to-end eCOA implementation projects for internal and external clients, overseeing scope, budgets, schedules, resources, quality, risks, documentation, vendors, and deliverables. Leads distributed project teams, maintains customer and stakeholder relationships, provides technical direction, reports project status to sponsors and management, and implements corrective actions and process improvements. Requires clinical research and GCP understanding, familiarity with EDC, eCOA, and IWRS technologies, strong communication and leadership skills, and international travel as needed.

Supports UK clinical trial start-up and site activation by collecting, reviewing, and preparing regulatory and site documents. Responsibilities include ICF adaptations, submission package preparation, regulatory green-light readiness, investigative-site liaison, tracking documentation and timelines, and coordinating with regulatory, project management, and site activation teams. Ensures complete, accurate, and compliant submissions under ICH-GCP, UK regulations, and study-specific requirements.

Lead complex global, multi-regional clinical trials from start-up through close-out for renal, obesity and/or MASH. Provide strategic sponsor partnership, oversee timelines, budgets, quality, risks and regulatory compliance, direct cross-functional teams, and drive operational delivery to achieve study objectives.

Lead strategy, vision, and delivery of a cloud-native SaaS data processing solution for life sciences and healthcare. Build and lead a data management team, drive product and go-to-market strategy, collaborate with engineering and partners, and deliver complex data pipelines and analytics capabilities across heterogeneous sources.

Manage pharmaceutical accounts across NHS health economies in the Southwest, Thames Valley, and Wales. Responsibilities include strategic account planning, formulary access, stakeholder engagement across primary and secondary care, market access, product uptake, patient pathway improvement, sales delivery, cross-functional collaboration, and compliance with the ABPI Code of Practice.

Conducts clinical coding audits, data-quality reviews, benchmarking, and deep-dive analyses for healthcare clients. Produces reports and dashboards, leads SHMI and clinical quality initiatives, facilitates clinician engagement, and provides training on coding, casemix, and data interpretation. Oversees coding services, supports operational quality and productivity, advises clients, develops CCA products, and manages consulting projects and workstreams.

Lead procurement governance, vendor qualification, and third-party risk management. Drive TPRM framework maturity, process transformation, automation/AI enablement, stakeholder governance, metrics, and cross-functional change initiatives.