Consultant, Global HTA
About the role
This vacancy has now expired. Please click here to view live vacancies.
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
Impactful work. Meaningful careers. Quality rewards.
At ICON, our employees are our greatest strength. That’s why we are committed to empowering you to live your best life, both inside and outside of work. Whether your ambition is lead a global team, become a deep scientific or technical expert, work in-house with our customers or gain experience in a variety of different ICON functions, we will support you in realising your full potential. Learn more about Our Culture at ICON
Day in the life
Teaser label
Career ProgressionContent type
BlogsPublish date
11/26/2025
Summary
How Clinical Research Job Seekers Can Enhance Their Applications Finding the right role in clinical research has become increasingly competitive as organisations continue to expand their study por
Teaser label
Inside ICONContent type
BlogsPublish date
11/14/2025
Summary
Building Bridges in Clinical Research: Daniela's Journey at ICON Daniela Rocco's career in clinical research has been driven by something straightforward but powerful: connection. From her e
Teaser label
Our PeopleContent type
BlogsPublish date
11/14/2025
Summary
Karina Espinoza's Journey at ICON Karina Espinoza's career in pharmacovigilance didn't begin with a grand plan. It started with a practical problem during her final year of a PhD in epidemiology, a
Similar jobs at ICON
Salary
Location
Turkey, Ankara
Location
Ankara
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
We are currently seeking a Clinical Research Associate II to join our diverse and dynamic team. As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing cli
Reference
JR139833
Expiry date
01/01/0001
Author
Tuba SuAuthor
Tuba SuSalary
Location
Poland, Warsaw
Location
Sofia
Prague
Dublin
Warsaw
Bucharest
Remote Working
Office or Home
Business Area
ICON Full Service & Corporate Support
Job Categories
Contracts Administration
Job Type
Permanent
Description
As a Site Contracts Lead, you will take ownership of site contracts for assigned studies at country, regional, or global level. You’ll play a pivotal role in enabling clinical trials to start on time,
Reference
JR139947
Expiry date
01/01/0001
Author
Magda KozuszekAuthor
Magda KozuszekSalary
Location
Turkey, Ankara
Location
Ankara
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
We are currently seeking a Clinical Research Associate II to join our diverse and dynamic team. As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing cli
Reference
JR139413
Expiry date
01/01/0001
Author
Tuba SuAuthor
Tuba SuSalary
Location
Brazil, Sao Paulo
Department
Clinical Monitoring
Real World Solutions
Location
Sao Paulo
Remote Working
Office or Home
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
We are currently seeking CRAs II and Senior CRAs to join our diverse and dynamic team. As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials
Reference
JR133497
Expiry date
01/01/0001
Author
Ana LuciaAuthor
Ana LuciaSalary
Location
Germany, Frankfurt
Location
Frankfurt
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
We are currently seeking a Clinical Research Associate II to join our diverse and dynamic team. As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing cli
Reference
JR137615
Expiry date
01/01/0001
Author
Roxana RoscaAuthor
Roxana RoscaSalary
Location
US, Blue Bell (ICON)
Department
Clinical Monitoring
Location
Oregon
Colorado
California
Arizona
New Mexico
Blue Bell
Idaho
Nevada
Utah
Washington
Remote Working
Office or Home
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
We are currently seeking a Senior Clinical Research Associate or Clinical Research Associate II to join our diverse and dynamic team. As a Clinical Research Associate at ICON, you will play a pivotal
Reference
JR138756
Expiry date
01/01/0001
Author
Ana LuciaAuthor
Ana Lucia