JUMP TO CONTENT

Senior Consultant - Global Value Communications

JR067851

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

List #1

Day in the life

Two computer monitors with data graphs
How Data Moves Through a Clinical Trial

Teaser label

Industry

Content type

Blogs

Publish date

12/01/2025

Summary

How Data Moves Through a Clinical Trial Clinical research depends on one essential element: trustworthy data. Every safety decision, every statistical conclusion and every regulatory submission i

Teaser label

Discover how data flows through a clinical trial and learn where your skills could fit within clinical research.

Read more
Male and female auditing a manufacturing facility
Quality and Compliance - A Plain Language Guide

Teaser label

Industry

Content type

Blogs

Publish date

11/28/2025

Summary

Quality and Compliance for New Entrants:           A Plain Language Guide Quality and compliance can feel like dense subjects when you are entering clinical research for the first time. Many job

Teaser label

A clear, practical introduction to quality and compliance for those starting a career in clinical research.

Read more
Female using a laptop to search for jobs
Improving Your Visibility in the Clinical Research Job Market

Teaser label

Career Progression

Content type

Blogs

Publish 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

Discover the search terms recruiters use most often and practical steps that can help candidates strengthen their visibility.

Read more
View all

Similar jobs at ICON

Visualisation Developer

Salary

Location

Ireland, Dublin

Location

Budapest

Dublin

Vilnius

Warsaw

Johannesburg

Tallinn

Kenya

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Data Scientist Lead

Clinical Programming

Job Type

Permanent

Description

We are currently seeking a Visualization Developer to join our diverse and dynamic team. As a Visualization Developer at ICON Strategic Solutions, you will be instrumental in leading the development a

Reference

JR134568

Expiry date

01/01/0001

Jack Fisher

Author

Jack Fisher
Jack Fisher

Author

Jack Fisher
Read more Shortlist Save this role
Study Manager - Home Health

Salary

Location

Poland, Gdansk

Location

Gdansk

Remote Working

Office Based

Business Area

ICON Full Service & Corporate Support

Job Categories

Project/ Program Management

Job Type

Permanent

Description

Job Advert PostingAt ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’

Reference

JR138203

Expiry date

01/01/0001

Lourdes Roy Prats Read more Shortlist Save this role
Study Delivery Manager

Salary

Location

Brazil, Sao Paulo

Location

Sao Paulo

Mexico City

Remote Working

Office or Home

Business Area

ICON Strategic Solutions

Job Categories

Clinical Trial Management

Job Type

Permanent

Description

We are currently seeking a Clinical Trial Manager to join our diverse and dynamic team at ICON Plc. In this critical role, you will be responsible for overseeing the planning, execution, and successfu

Reference

JR139151

Expiry date

01/01/0001

Tulio Sanquiz

Author

Tulio Sanquiz
Read more Shortlist Save this role
Study Delivery Manager

Salary

Location

Poland, Warsaw

Location

Sofia

Prague

Budapest

Warsaw

Bucharest

Remote Working

Office or Home

Business Area

ICON Strategic Solutions

Job Categories

Clinical Trial Management

Job Type

Permanent

Description

We are currently seeking a Clinical Trial Manager to join our diverse and dynamic team at ICON Plc. In this critical role, you will be responsible for overseeing the planning, execution, and successfu

Reference

JR139155

Expiry date

01/01/0001

Dagmara Drozdowska Read more Shortlist Save this role
PROJECT ASSOCIATE

Salary

Location

Mexico, Mexico City

Location

Mexico City

Remote Working

Office Based

Business Area

ICON Full Service & Corporate Support

Job Categories

Project/ Program Management

Job Type

Permanent

Description

We are currently seeking a Project Associate to join our diverse and dynamic team. As a Project Associate at ICON, you will play a pivotal role in providing key administrative support in clinical oper

Reference

JR140439

Expiry date

01/01/0001

Ana Lucia

Author

Ana Lucia
Ana Lucia

Author

Ana Lucia
Read more Shortlist Save this role
Inhouse CRA

Salary

Location

Netherlands, Utrecht, Zen

Location

Utrecht

Remote Working

Office or Home

Business Area

ICON Strategic Solutions

Job Categories

Clinical Trial Support

Job Type

Permanent

Description

We are seeking a motivated Clinical Trial Administrator to join our strong and dynamic team. In this role, you will be an essential contributor to the planning and execution of clinical trials, suppor

Reference

JR140418

Expiry date

01/01/0001

Vanessa Verdickt Read more Shortlist Save this role
View Jobs

Browse popular job categories below or search all jobs above