JUMP TO CONTENT

Senior Investigator Pricing Analyst

JR072426

About the role

This vacancy has now expired. Please click here to view live vacancies.

Job Title: Investigator Pricing Analyst I

Location: Dublin 18 / USA

At ICON, it's our people that set us apart.

As a global provider of drug development solutions, our work is serious business. But that doesn't mean you can't have fun while you do it. With our vision to be the partner of choice in drug development, we hire only the best and brightest in the industry! Are you one of them?

At ICON, we have an incredible opportunity for an Investigator Pricing Analyst I to join the team in our Leopardstown, Dublin 18 location.

Role Summary:

To develop, interpret and define investigator site budget assumptions based on clinical trial protocols for internal and external clients.

* You must have CRO contract/budget experience, specific to site contracts, along with protocol review experience to be considered for this role

The Role:

People - Leadership, Teamwork, Energising and Developing Others

  • To positively contribute to the investigator Pricing Strategy Group (PSG) by seeking to improve their job performance and knowledge of investigator budget pricing strategies and ICON systems and processes
  • Provide expert guidance to ICON colleagues and external clients regarding fair market value fees for research related procedures/non-procedures and general investigator site budget formatting
  • To effectively build and maintain a productive working relationship with the Clinical teams and other department staff to effectively manage their needs and expectations in relation to investigator budget pricing.

Clients - Delivery to Customers, Building Relationships

  • Translate clinical trial protocol required procedures to relevant Current Procedural Terminology (CPT) codes in order to appropriately apply fair market value costs
  • Prepare communication materials/ payment data for internal/ external clients relating to investigator budget pricing /reporting as appropriate
  • Conduct day-to-day activities in a service-oriented, client-oriented and professional manner
  • Maintain positive strong working relationships with clients, vendors and staff
  • To escalate pricing issues/delays appropriately
  • To set up, organize and maintain investigator budget pricing and supporting documentation as appropriate.
  • Work with line manager as required to quality check /review work completed and maintain standards of excellence

Performance - Personal Effectiveness, Commercial Awareness, Robust Thinking

  • Oversee and be accountable for the quality of the investigator pricing budget generated for internal/external protocols assigned ensuring that it is conducted in an effective manner, meeting agreed timelines and expectations and in accordance with industry/ internal KPIs, WPS and SOPs, appropriate regulations and ICON's quality standards.
  • Develop investigator site budget estimates for each country per feasibility specifications according to available protocol information and fair market value costs
  • Liaise with Business Development department to establish and provide required investigator fee estimates for inclusion in final RFP bid grid
  • Liaise with internal/sponsor project lead to finalize budget formatting and costs per country, in the appropriate currencies
  • Interpret final protocol, where available, to develop master budget templates.
  • Provide ballpark estimations on projects where minimal information is available from the client based on experiential and historical data in similar projects
  • Revise estimates as necessary in line with feedback and requests for RFP recosts
  • Update estimates based on feedback from clinical experts internally or with the client and record this feedback appropriately
  • Provide expert information and relevant documentation in relation to general pricing processes , fair market value costs, benchmark database systems (e.g. GrantPlan) and general investigator budget processes
  • Attend project specific and general meetings as needed
  • Liaise with ICON SSU during site agreement negotiations to assist with formatting/cost questions
  • Special projects/assignments as requested.
  • Communicate with assigned project lead to establish realistic timelines that will allow sufficient time to ensure quality outputs in line with business expectations.
  • Contribute to writing/updating PSG SOP's/ WP's as requested
  • Conduct general and study specific training for Clinical staff assigned to the studies / presentations to Clinical teams and to other ICON departments where necessary.
  • Liaise with all other ICON departments such as Clinical, IPG, PTS, IT, Finance, legal and contracts to ensure pricing queries are speedily resolved and that the necessary preventative measures are put in place to prevent recurrence of similar issues.
  • Accurately record and update all applicable logs and maintain all tracking tools as requested.
  • Send meeting requests, book meeting rooms / teleconference facilities for meetings as required.
  • Record, prepare and distribute meeting minutes as requested
  • Be familiar with industry standards, appropriate regulations and relevant ICON processes and procedures
  • Contribute to process improvement initiatives within the group and the wider organisation
  • Meet all PSG iLearn/training requirements appropriate to this position.
  • Ensure ICON's reputation for excellence is carried through and maintained throughout all processes and highlight areas for improvement as needed

What you will need:

  • Bachelor's degree or local equivalent preferred, or will have relevant experience for the position
  • Ability to liaise successfully with all levels of management at ICON, vendors, and clients.
  • Good working knowledge of PC applications (Excel, Word, Outlook and Access).
  • Excellent organizational, administration and problem solving skills.
  • Excellent written and verbal communication skills.
  • Excellent Customer Relationship Management skills
  • Ability to easily adapt to dynamic environment working to strict deadlines and targets.
  • Good numerical ability an advantage.

#LI-CW1

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

RBQM Manager

Salary

Location

India, Chennai

Location

Bangalore

Chennai

Bengaluru

Remote Working

Hybrid

Business Area

ICON Full Service & Corporate Support

Job Categories

Project/ Program Management

Job Type

Permanent

Description

Job role - RBQM ManagerAbout the RoleWe are seeking an experienced and forward-thinking Risk-Based Quality Management (RBQM) Manager to lead the implementation and execution of proactive, risk-focused

Reference

JR135865

Expiry date

01/01/0001

Shrayashi Ghosh Read more Shortlist Save this role
Clinical Site Associate

Salary

Location

Israel, Tel Aviv

Department

Clinical Monitoring

Location

Tel Aviv

Remote Working

Hybrid

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

JR145242

Expiry date

01/01/0001

Tereza Svobodova Read more Shortlist Save this role
Analytical Monitor

Salary

Location

India, Bangalore

Location

Bangalore

Chennai

Trivandrum

Bengaluru

Remote Working

Hybrid

Business Area

ICON Strategic Solutions

Job Categories

Clinical Data Management

Job Type

Permanent

Description

We are currently seeking an Analytical Monitor (Advanced Level) to join our dynamic and expanding client-dedicated Integrated Data Analytics & Reporting team. In this role, you will play a pivotal par

Reference

JR144388

Expiry date

01/01/0001

Abhisikta Mishra Read more Shortlist Save this role
Set Up Specialist

Salary

Location

Ireland, Dublin

Department

Full Service - Development & Commercialisation Solutions

Location

Sofia

Dublin

Remote Working

Hybrid

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Project Management

Job Type

Permanent

Description

We are currently seeking a Set Up Specialist I (SUS) to join our diverse and dynamic team. As a SUS at ICON Central Laboratories (ICL), you will play a pivotal role in setting up the laboratory requir

Reference

JR140308

Expiry date

01/01/0001

James Smith

Author

James Smith
James Smith

Author

James Smith
Read more Shortlist Save this role
Clinical Research Associate

Salary

Location

Netherlands, Utrecht, Zen

Department

Clinical Monitoring

Location

Utrecht

Remote Working

Remote or Office

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

At ICON plc, we partner with the world’s leading pharmaceutical organizations to accelerate the development of transformative therapies. Within our Large Pharma division, we deliver global scale, oper

Reference

JR145246

Expiry date

01/01/0001

Sophie Clarke

Author

Sophie Clarke
Read more Shortlist Save this role
Site Partner II/Senior Site Partner

Salary

Location

US, Blue Bell (ICON)

Location

Boston

Cary

Chicago

Lexington

Los Angeles

Nashville (TN)

Portland

Salt Lake City

San Antonio

Whitesboro

Raleigh

Houston

Winston-Salem

Knoxville

Charlotte

Mt. Pleasant

Hickory

Rocky Mount

New York

Bristol

Wilmington

Salisbury

Downers Grove

McFarland

Blue Bell

Lenexa

Piedmont

Rochester

Long Beach

Remote Working

Remote or Office

Business Area

ICON Full Service & Corporate Support

Job Categories

Study Start Up

Job Type

Permanent

Description

Title: Site Partner IIRole Summary:Accountable for the proficient and proactive co-ordination of all necessary activities required to achieve timely site activations and maintenance tasks for any give

Reference

JR145331

Expiry date

01/01/0001

Kris Costello

Author

Kris Costello
Read more Shortlist Save this role
View Jobs

Browse popular job categories below or search all jobs above