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IQVIA

Runs drug trials and sells health data to pharma

Associate Director - Health Technology Assessment, Global Health Economics Team

Risk, Regulatory & Legal AdvisoryConfirmed live in the last 24 hours
Full-time

About the Job

Requirements

  • Postgraduate degree-level education or higher in a relevant discipline, such as health technology assessment, health economics, economics, life sciences, epidemiology, biostatistics, public health, medicine, or pharmacy.
  • Typically, 8 or more years of relevant experience in consulting, the pharmaceutical sector, an HTA agency, academia, or a related environment.
  • Extensive experience preparing evidence strategies and submissions aligned with HTA processes and requirements in the UK and/or Europe, including involvement in appraisal, scientific advice, or negotiation processes where relevant.
  • Demonstrated success managing complex client engagements, multidisciplinary teams, and portfolios of projects.
  • A strong commercial track record, including client relationship development, proposal leadership, scope and budget development, and contribution to business generation.
  • Demonstrable commercial awareness and a thorough understanding of the pharmaceutical and life sciences industry.
  • Strong people leadership, coaching, and capability-development skills.
  • Strategic thinking and attention to detail.
  • Excellent written and verbal communication skills, with fluency in English; applications should be submitted in English.

Responsibilities

  • Act as a senior strategic advisor to pharmaceutical, biotechnology, and medical device clients on HTA evidence planning, market access strategy, and reimbursement optimisation.
  • Lead the design and delivery of complex, high-value global and regional HTA programmes with limited senior oversight.
  • Guide clients through evolving HTA requirements, including EU Joint Clinical Assessments, national HTA submissions, early scientific advice, evidence planning, and reimbursement processes.
  • Shape and evolve HTA consulting offerings in collaboration with the Centre of Excellence for HTA Evidence and Strategy and the wider senior leadership team.
  • Identify emerging HTA and market access trends and translate them into relevant client solutions.
  • Develop and maintain senior-level client relationships, act as a trusted advisor, and identify opportunities to expand existing accounts and build new relationships.
  • Support HTA-related business development opportunities, including proposal development, scope definition, pricing, and contract discussions, with appropriate senior input.
  • Provide executive oversight across multiple concurrent projects and programmes, ensuring scientific quality, strategic relevance, client satisfaction, and commercial performance.
  • Lead senior client discussions, steering committee interactions, problem solving, negotiation, and risk mitigation across complex engagements.
  • Work collaboratively with internal teams, including technical consultants generating HTA evidence and teams in Market Access, Patient-Centered Solutions, HTA Accelerator Solutions, database studies, and local teams globally.
  • Act as a role model, coach, and mentor for consultants, senior consultants, and emerging leaders, creating opportunities that support their career development as HTA specialists.
  • Support recruitment, onboarding, performance management, succession planning, and capability development across the team.
  • Provide formal line management responsibilities, as appropriate.
  • Lead and contribute to HTA thought leadership, including conference abstracts and posters, white papers, peer-reviewed publications, and external presentations.
  • Represent IQVIA at relevant industry conferences, scientific meetings, client forums, and other external events.

Desired Qualifications

  • An established network of health economics, outcomes research, HTA, or market access contacts.
  • Previous line management experience.
  • Previous experience in a consultancy environment.
  • Strong understanding of clinical trial design, statistical methods used in clinical trials, and evidence synthesis methodology.
  • Quantitative skills, including biostatistics and health economic modelling methods, and good knowledge of statistical software packages such as STATA and R.

About the Company

IQVIA

Runs drug trials and sells health data to pharma

IQVIA runs clinical trials for drug, biotech and medical device companies and sells them the health data, software and analytics they use to develop and market treatments. Its research arm designs studies, recruits trial sites and patients, and manages trials through to regulatory filing. Its commercial arm sells market data, consulting and software that pharma sales and marketing teams use to plan product launches. Clients pay through multi-year service contracts and data and software subscriptions. IQVIA was formed in 2016 when clinical research firm Quintiles merged with health data company IMS Health, and it is based in Durham, North Carolina.

Company size
10,001+
Company stage
IPO
Headquarters
Durham, NC
Founded
1998

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