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Consultant, Global HTA

JR064364

About the role

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Consultant, Global HTA, Health Economics Reimbursement and Outcomes

Location: UK (Home based), Nanterre (France), Warsaw (Poland), Amsterdam (NL)

Are you looking for an exciting opportunity to work within a dynamic, collaborative environment with a team committed to being an industry-leading provider?

'At ICON, our value is our people, who consistently deliver the highest-quality work to our clients'

The Consultant HTA supports the life cycle of projects in the group around study design, project management, data collection, data management, data analysis, data interpretation, and reporting.

Who Are We?

The global team are made up of HTA, HEOR, medical communications experts and market access consultants, who specialize in helping our clients engage with HTA/reimbursement agencies, payers and achieve patient access for their products. ICON is a fast-growing global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries, known for its innovative approach. ICON's commercialization and outcomes capabilities coupled with our strategic consultancy services has built the industry's most integrated product development, clinical communications and market access solutions. This means more growth and career opportunities for our current and future employees.

Responsibilities:

Scientific

  • Develops approach to assigned piece(s) of the research problem, e.g. study design, with limited direction
  • Reviews appropriate literature searches and critiques of studies.
  • Develops literature search strategy
  • Reviews and develops model protocol/analysis and key opinion leader interview guides with limited direction
  • Oversees data collection and management, including efficient and effective delegation and oversight; conducts primary data collection, including moderating or co-moderating advisory boards and/or conducting one-on-one key opinion leader interviews
  • Develops and structures specific content. Writes outline, and reviews final draft of analysis plan
    Oversees development of first drafts of analysis plans including tables, listings and figures
  • Oversees cleaning of data, conduct of simple quantitative analysis, and write up of results
    Independently prepares near-final drafts of client deliverables, and basic report sections and first drafts of dossiers, statistical analysis plans, gap analyses, complex report sections, and manuscripts
  • May co-author presentations for scientific conferences and manuscripts for scientific journals
    Supports other project activities as needed, completes internal documentation and quality-checks the work of others

Project/Risk Management

  • Oversees vendor management, including scope of work development, contract initiation, and project milestones, timelines, deliverables, and budgets

  • Assumes primary responsibility for day-to-day tasks related to the project, including making decisions related to the project either alone or in conjunction with more senior staff

  • Involved with client communication, and may be primary point of contact with client
    Efficiently delegates and communicates with project team, and ensures proper staffing and oversight on projects

  • Tracks timelines and keeps project team and PI informed in order to complete work within the expected timeframe

  • Maintain understanding of project requirements and identifies scope creep as it happens. Alerts business operations and project director to the need for a change order at appropriate times.
    Support business operations on projects as needed

  • Identifies project risks and/or risks across multiple deliverables and effectively executes project risk mitigation strategies

To be successful you will have:

  • Significant experience in the delivery of HTA, market access and health outcomes projects
  • Proven ability to manage multiple client projects

Technical Requirements

  • Excellent working knowledge of regional market access requirements, global HTA submission requirements, payer interviewing, facilitating advisory boards, and value proposition development
  • Good working knowledge of health economic evaluation and systematic literature review methods

Qualifications

  • A Ph.D./ Master's degree in economics, health policy, public health or a related discipline
  • Strong proven experience in a consulting or pharmaceutical industry setting
  • Excellent communication skills, both verbally and in writing as well as an established ability to work independently or as part of a team
  • High level of organizational and project management skills combined with demonstrated self-motivation, business sense, sound judgement and an analytical approach
  • Proficiency in planning and motivating others as well as superior interpretative and innovation thinking skills
List #1

Day in the life

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Driving Trials Forward: Study Start-Up Leadership at ICON

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Publish date

03/16/2026

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Driving Study Start-Up: James Pereira's Journey at ICON James Pereira's career in clinical research has been shaped by a single driving question: how do we get studies started faster? From his earl

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Explore James Pereira's career in study start-up at ICON, leading global teams to accelerate patient access.

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Who’s Who in a Clinical Trial Team

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03/15/2026

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Who's Who In a Clinical Trial Team Clinical trials rely on large, cross functional teams working together across countries, time zones and specialisms. For those new to the industry, the number of

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Learn how clinical trials are delivered by understanding the roles of sponsors, CROs, and sites.

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