Jobs at IQVIA

Lead end-to-end delivery of real-world observational oncology studies within a pharma FSP, managing cross-functional teams, vendors, study documentation, timelines, budgets, risks, and regulatory compliance while generating reports and driving continuous improvement.

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.

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.

Leads strategic advisory consulting engagements for life sciences clients, partnering with VP-level stakeholders on strategic, technology, and operational challenges. Responsibilities include integrated solution design, client relationship development, revenue growth, proposal development, thought leadership, industry analysis, team leadership, mentoring, and capability building. The role translates AI/ML, digital health, real-world evidence, and data interoperability trends into actionable client strategies.

Owns the strategic direction, vision, roadmap, requirements, and lifecycle management for IQVIA Patient Technology products. Leads market assessment, product innovation, engineering backlog prioritization, implementation strategies, financial performance, proposals, and executive client oversight. Partners with engineering, technical, procurement, business, and leadership teams to deliver products aligned with company goals and quality standards.

Manage key Primary Care accounts to increase awareness and referrals for Women’s Health treatments. Deliver education, develop referral pathways, run face-to-face and virtual meetings, and create territory plans to improve patient access and outcomes.

Provide specialist clinical pharmacy and independent prescribing support for ATTR-CM patients. Run virtual clinics, review treatment response, optimise guideline-directed heart failure therapy, perform risk stratification and escalation, educate patients/carers and liaise with multidisciplinary teams, primary care and homecare providers to deliver coordinated care.

Drive growth of the Expert Ecosystem SaaS platform by acquiring new clients and expanding existing accounts within pharma/biotech. Manage full sales cycle, develop account and territory plans, build proposals with delivery teams, and maintain senior stakeholder relationships. Support go-to-market, market intelligence, and demand-generation activities while ensuring smooth transition from sale to implementation and pursuing renewals and upsell opportunities.

Field-based role building relationships with independent pharmacies to drive OTC product sales. Plan territory visits, execute in-store merchandising, record activity in CRM, follow compliance and pharmacovigilance procedures, and attend bi-monthly sales meetings (overnight required). Training and coaching provided.

Lead strategic advisory engagements for life sciences clients, designing integrated solutions that combine strategy, data, and technology. Build VP+ client relationships, drive revenue, mentor teams, translate technologies (AI/ML, digital health, RWE) into strategic recommendations, and contribute to thought leadership and practice development.

Manage clinical trial data for Phase I-III per ICH/GCP: perform ongoing data review and reconciliation (including third-party streams and SAE reconciliation), execute UAT and QC of clinical databases, and update data-management documentation to ensure quality deliverables and timelines.

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.

Serve as primary data management lead for Phase I-III trials: design CRFs/edit checks, write DMPs, oversee UAT/QC, manage data review/discrepancy resolution, coordinate with programmers/vendors, train staff, archive trials, and ensure GCP/regulatory compliance.

Monitor Phase I-IV clinical trials: perform site evaluation, initiation, interim and close-out visits; ensure GCP/ICH compliance; verify source data and eCRF/EDC entries; prepare monitoring reports; coordinate with CTM/Lead CRA and sites; support investigator meetings and training. Oncology monitoring experience required. Freelance role with travel across the UK.

Manage FIC projects including buy-/sell-side due diligence, valuation, asset screening and growth strategy. Lead project teams, oversee research, QC deliverables, present findings to clients, support business development and team development.

Lead scientific translation of COA scoring manuals into validated, implementation-ready scoring algorithms and interpretation guidance. Define missing-data rules, resolve scoring ambiguities, partner with statisticians and engineers, investigate discrepancies, and develop standardized documentation, SOPs, and governance to scale scoring solutions.

Lead a national sales team of Specialist KAMs to drive adoption of an oncology therapy. Recruit, coach, and monitor team performance; develop and execute sales strategies; manage key customer relationships; and align commercial activities with marketing and medical teams to meet revenue and market-share targets.

Lead and manage the local biostatistics and statistical programming functions globally, ensuring high-quality deliverables, regulatory engagement, budgeting, staffing, proposal development, client relationship growth, and process improvements. Provide scientific and technical biostatistical oversight on complex clinical studies, represent clients at regulatory meetings, and drive strategy, risk management, and training across the department.

Lead cross-portfolio implementation of Population Health initiatives for COA portfolio: translate strategy into roadmaps, governance, readiness frameworks, and scalable operating models; coordinate cross-functional stakeholders (standards, EHR, data platforms, delivery, sales); manage risks, dependencies, and evidence/adoption frameworks; support health-system, registry, and pilot enablement; drive continuous improvement and align implementation with scientific and commercial priorities.