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

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
Headshot of female
From Lab Bench to Program Leadership: Sinéad McKeon's Career at ICON

Teaser label

Our People

Content type

Blogs

Publish date

02/05/2026

Summary

Building expertise through diverse roles and continuous learning Sinéad McKeon's career at ICON demonstrates how scientific training can evolve into strategic leadership. Now a Senior Manager in Lab

Teaser label

Discover how a career can evolve from hands on lab work to program management in this interview with Sinéad McKeon.

Read more
Headshot image of male
Shaping the Future of Patient Safety: A Conversation with Hassan Aljobori

Teaser label

Our People

Content type

Blogs

Publish date

02/05/2026

Summary

Shaping the Future of Patient Safety At ICON, patient safety is the foundation of everything we do. Hassan Aljobori, Director of Pharmacovigilance, shares his journey through nine years of growth

Teaser label

Hassan shares his career journey, advice for building a career in pharmacovigilance, and what sets ICON apart as an employer.

Read more
View all

Similar jobs at ICON

Lab Analyst II

Salary

Location

US, Lenexa KCIB (PRA)

Department

Full Service - Early Clinical and Bioanalytical Solutions

Location

Lenexa

Remote Working

Office Based

Business Area

ICON Full Service & Corporate Support

Job Categories

Laboratory Support

Job Type

Permanent

Description

We are currently seeking a Lab Analyst II to join our diverse and dynamic team. As a Lab Analyst II at ICON, you will be responsible for performing intermediate-level laboratory tests and analyses to

Reference

JR142793

Expiry date

01/01/0001

Hanna Pitcairn Read more Shortlist Save this role
Customer Service Rep

Salary

Location

Ireland, Limerick

Location

Limerick

Remote Working

Office Based

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Trial Support

Job Type

Permanent

Description

ICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotech

Reference

JR141739

Expiry date

01/01/0001

Katty Barreto Maia Read more Shortlist Save this role
Regional Manager of Clinical Investigator Payments

Salary

Location

Brazil, Sao Paulo

Location

Sao Paulo

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Accounting & Finance

Job Type

Temporary Employee

Description

We are currently seeking a Regional Manager of Clinical Investigator Payments to join our diverse and dynamic team. As a Manager, Investigator Payments at ICON, you will oversee and manage the investi

Reference

JR143065

Expiry date

01/01/0001

Tulio Sanquiz

Author

Tulio Sanquiz
Read more Shortlist Save this role
Senior Clinical Pharmacologist

Salary

Location

UK, Reading

Location

Copenhagen

Paris

Frankfurt

Dublin

Milan

Warsaw

Lisbon

Barcelona

Reading

Mechelen

Assen

Remote Working

Office or Home

Business Area

ICON Strategic Solutions

Job Categories

Clinical Trial Management

Job Type

Temporary Employee

Description

We are currently seeking a Director, Clinical Pharmacology to join our diverse and dynamic team. As a Director, Clinical Pharmacology at ICON, you will play a pivotal role in leading the design, execu

Reference

JR144374

Expiry date

01/01/0001

Jonathan Cunliffe Read more Shortlist Save this role
Manager, TMF

Salary

Location

United States of America

Location

Multiple US Locations

Boston, MA

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Document Management

Job Type

Permanent

Description

The Manager, Trial Master File (TMF) is responsible for the strategic oversight, operational management, and continuous improvement of the Trial Master File across clinical studies. This role ensures

Reference

JR143731

Expiry date

01/01/0001

Kala Murphy

Author

Kala Murphy
Kala Murphy

Author

Kala Murphy
Read more Shortlist Save this role
Clinical Site Associate Portugues

Salary

Location

Spain, Barcelona

Department

Clinical Monitoring

Location

Barcelona

Remote Working

Office Based

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

JR144765

Expiry date

01/01/0001

Lourdes Roy Prats Read more Shortlist Save this role
View Jobs

Browse popular job categories below or search all jobs above