Senior Investigator Pricing Analyst
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
Impactful work. Meaningful careers. Quality rewards.
At ICON, our employees are our greatest strength. That’s why we are committed to empowering you to live your best life, both inside and outside of work. Whether your ambition is lead a global team, become a deep scientific or technical expert, work in-house with our customers or gain experience in a variety of different ICON functions, we will support you in realising your full potential. See all locations Learn more about Our Culture at ICON
Day in the life
.png)
Teaser label
IndustryContent type
BlogsPublish date
07/07/2025
Summary
Precision at the Outset: The Strategic Role of Site Selection and Activation in Clinical Trials The success of any clinical trial begins well before the first patient is enrolled. Behind every sit
.png)
Teaser label
IndustryContent type
BlogsPublish date
07/04/2025
Summary
Cybersecurity in Clinical Data Management In clinical research, data is both a vital asset and a significant responsibility. As trials become increasingly digitised and decentralised, the protectio
.png)
Teaser label
IndustryContent type
BlogsPublish date
07/03/2025
Summary
Finding the Specialisation for You Clinical research is a dynamic, multidisciplinary field that brings together scientific innovation, operational rigour and patient-centric thinking. While many
Similar jobs at ICON
Salary
Location
Netherlands, Assen
Department
Full Service - Early Clinical and Bioanalytical Solutions
Location
Assen
Remote Working
Office Based
Business Area
ICON Full Service & Corporate Support
Job Categories
Program Management
Job Type
Permanent
Description
We zijn nu op zoek naar een Project Manager II EDS om ons team in Groningen te versterken. Als je een gedreven persoon bent die gedijt in een dynamische en ondersteunende omgeving, nodigen we je uit o
Reference
JR132376
Expiry date
01/01/0001
Author
Rowena DeswertAuthor
Rowena DeswertSalary
Location
Canada
Department
Clinical Operations Roles
Location
Canada
Remote Working
Home-Based
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
As a Clinical Quality Compliance Lead you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
Reference
2025-120615
Expiry date
01/01/0001
Author
Melissa BennerAuthor
Melissa BennerSalary
Location
India, Trivandrum
Location
Trivandrum
Remote Working
Office Based
Business Area
ICON Full Service & Corporate Support
Job Categories
Accounting & Finance
Job Type
Permanent
Description
We are currently seeking a Supervisor, Accounts Receivable to join our diverse and dynamic team. As a Supervisor, Accounts Receivable at ICON, you will oversee the accounts receivable process, ensurin
Reference
JR129526
Expiry date
01/01/0001
Author
Preetha SureshAuthor
Preetha SureshSalary
Location
Poland
Department
Clinical Monitoring
Location
Poland
Remote Working
Home-Based
Business Area
ICON Strategic Solutions
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
As a Senior CRA, you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
Reference
2025-120880
Expiry date
01/01/0001
Author
Dagmara DrozdowskaAuthor
Dagmara DrozdowskaSalary
Location
Israel
Department
Clinical Operations Roles
Location
Israel
Remote Working
Home-Based
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotech
Reference
2025-120870
Expiry date
01/01/0001
Author
Salome KankiaAuthor
Salome KankiaSalary
Location
Spain, Poland
Department
Clinical Trial Management
Location
Poland
Spain
Remote Working
Home-Based
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Management
Job Type
Permanent
Description
We currently have an exciting new opportunity for an experienced Global Clinical Project Manager within the Oncology team to join a successful sponsor dedicated program. We are looking for a Global Cl
Reference
2025-120517
Expiry date
01/01/0001
Author
Tanzina GuerniAuthor
Tanzina Guerni