Senior Consultant - Global Value Communications
About the role
This vacancy has now expired. Please click here to view live vacancies.
Senior Consultant, Global HTA and Value Communications
Location: Home based in UK or US (East Coast)
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 Senior Consultant supports the life cycle of projects in the group including leading efforts 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, including our ex Mapi colleagues 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
· Develops and reviews literature review 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 HTA and Value communications' deliverables (HAT dossier, Global Value dossier…) . Oversees development of first drafts of these deliverables including tables, listings and figures
· Oversees cleaning of data, conduct of simple quantitative qualitative 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 journal
· Supports other project activities as needed, completes internal documentation and quality-checks the work of others
Client development
· Drafts sections of proposal documents with increasing level of autonomy, including costing/budgeting
· Maintains broad understanding of the nature and challenges with specific client relationships and supports the building/broadening of these relationships where appropriate
· Contributes to BD meetings, conferences and other BD initiatives with increased autonomy and complexity and develop sound recommendations helping clients meet their goals
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
· 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 leading, developing and managing a team of researchers working in a consultancy environment
- Significant experience in the delivery of HTA, value communications/market access and health outcomes projects
- Proven ability to manage multiple client projects
- Excellent working knowledge of regional market access requirements, global HTA submission requirements, payer interviewing, facilitating advisory boards, and value proposition development- especially in France
- Good working knowledge of health economic evaluation and systematic literature review methods
- A Ph.D./ Master's degree in economics, health policy, public health or a related discipline (preferred)
- 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
#LI-ICO1
Explore more about ICON
Day in the life
Teaser label
IndustryContent type
BlogsPublish date
07/22/2026
Summary
Clinical Trials: From Protocol to Patient Clinical trials are essential to the development of new medicines and treatments, yet the way they work is often misunderstood. For those considering a ca
Teaser label
IndustryContent type
BlogsPublish date
07/21/2026
Summary
A Beginner's Guide to Drug Safety When most people think about careers in clinical research, roles like Clinical Research Associate or Clinical Trial Manager usually come to mind. But there's ano
Teaser label
Our PeopleContent type
BlogsPublish date
07/06/2026
Summary
Meet the CRA helping shape a new partnership Ask Rebeca Rojas Hernández what her dad tells people she does for a living and she can't help but smile. "He proudly tells everyone that I visit clinic
Similar jobs at ICON
Salary
Location
Canada, Burlington
Location
Burlington
Remote Working
Remote
Business Area
ICON Strategic Solutions (FSP)
Job Categories
Clinical Project Management
Job Type
Permanent
Description
We are currently seeking a Project Manager to join our diverse and dynamic team. As a Project Manager at ICON, you will be responsible for leading and coordinating project activities, ensuring that pr
Reference
JR155771
Expiry date
01/01/0001
Author
Kaitlyn LurkerAuthor
Kaitlyn LurkerSalary
Location
Canada, Burlington
Location
Burlington
Remote Working
Remote
Business Area
ICON Strategic Solutions (FSP)
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
What you will be doing Support Global Study Director (GSD) / Global Study Associate Director (GSAD) and Global Study Managers (GSMs) by completing delegated study work.Initiate and lead the set-up of
Reference
JR156253
Expiry date
01/01/0001
Author
Jonathan HolmesAuthor
Jonathan HolmesSalary
Location
Romania, Bucharest
Location
Bucharest
Remote Working
Remote or Office
Business Area
ICON Full Service & Corporate Support
Job Categories
Project/ Program Management
Job Type
Permanent
Description
What You Will Do:You will lead resource planning activities to ensure effective allocation of resources across assigned functions and portfolios, supporting business objectives and project delivery.Ke
Reference
JR156074
Expiry date
01/01/0001
Author
Maya KatsarskaAuthor
Maya KatsarskaSalary
Location
UK, Reading
Location
Madrid
Reading
Remote Working
Remote
Business Area
ICON Strategic Solutions (FSP)
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
As a Clinical Registry Coordinator at ICON Plc, you will be instrumental in ensuring the transparency and integrity of clinical trial data and results.What You Will Do: Key responsibilities include:Pr
Reference
JR156187
Expiry date
01/01/0001
Author
Rajvir SamraAuthor
Rajvir SamraSalary
Location
Poland, Warsaw
Location
Warsaw
Remote Working
Remote
Business Area
ICON Strategic Solutions (FSP)
Job Categories
Study Start Up
Job Type
Permanent
Description
As a Study Start Up Associate II at ICON, you will support the facilitation of site start up and communication with internal and external team members to ensure prompt site approval and study timeline
Reference
JR155788
Expiry date
01/01/0001
Author
Dagmara DrozdowskaAuthor
Dagmara DrozdowskaSalary
Location
Spain, Madrid
Department
Clinical Monitoring
Real World Solutions
Location
Barcelona
Madrid
Remote Working
Remote or Office
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
We are currently seeking a Clinical Site Associate to join our diverse and dynamic team. As a Clinical Site Associate at ICON, you will play a key role in supporting site management activities and ens
Reference
JR144259
Expiry date
01/01/0001
Author
Lourdes Roy PratsAuthor
Lourdes Roy Prats