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

Headshot image of male
Driving Trials Forward: Study Start-Up Leadership at ICON

Teaser label

Our People

Content type

Blogs

Publish date

03/16/2026

Summary

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

Teaser label

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

Read more
Male and female in lab
Who’s Who in a Clinical Trial Team

Teaser label

Inside ICON

Content type

Blogs

Publish date

03/15/2026

Summary

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

Teaser label

Understand the key roles in a clinical trial team, from study start up and site activation to data, safety and quality.

Read more
Nurse and patient
Understanding Roles in a Clinical Trial: Sponsors, CROs, and Sites

Teaser label

Industry

Content type

Blogs

Publish date

02/16/2026

Summary

What Sponsors, CROs, and Sites Each Do Clinical research brings together many organisations, each with a specific role in delivering a clinical trial. For those new to the industry, the relationsh

Teaser label

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

Read more
View all

Similar jobs at ICON

CTA

Salary

Location

Spain, Madrid

Location

Madrid

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Trial Support

Job Type

Permanent

Description

We are currently seeking a Clinical Trial Administrator to join our diverse and dynamic team. As a Clinical Trial Administrator at ICON, you will play a pivotal role in assisting with the design and a

Reference

JR147170

Expiry date

01/01/0001

Ana Guerra Garaeta Read more Shortlist Save this role
Clinical Trial Manager

Salary

Location

China, Beijing

Location

Beijing

Remote Working

Remote or Office

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

JR145776

Expiry date

01/01/0001

Sunshine Yang

Author

Sunshine Yang
Read more Shortlist Save this role
Senior CRA

Salary

Location

China, Changsha

Department

Clinical Monitoring

Location

Guangzhou

Shanghai

Wuhan

Changsha

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 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

JR142961

Expiry date

01/01/0001

Allen Hao

Author

Allen Hao
Allen Hao

Author

Allen Hao
Read more Shortlist Save this role
Clinical Research Associate I

Salary

Location

China, Shanghai

Location

Shanghai

Remote Working

Remote or Office

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

JR141842

Expiry date

01/01/0001

Sunshine Yang

Author

Sunshine Yang
Read more Shortlist Save this role
Clinical Research Associate

Salary

Location

Canada, Montreal

Location

Montreal

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

JR146393

Expiry date

01/01/0001

Jamie Pruitt

Author

Jamie Pruitt
Read more Shortlist Save this role
View Jobs

Browse popular job categories below or search all jobs above