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. Learn more about Our Culture at ICON
Day in the life
Teaser label
Our PeopleContent type
BlogsPublish date
11/14/2025
Summary
Karina Espinoza's Journey at ICON Karina Espinoza's career in pharmacovigilance didn't begin with a grand plan. It started with a practical problem during her final year of a PhD in epidemiology, a
Teaser label
Our PeopleContent type
BlogsPublish date
11/13/2025
Summary
A Career Built on Patient Impact: Victoria DeVeaugh Geiss's Journey at ICON Victoria DeVeaugh Geiss has spent more than two decades in clinical research, and one thing has stayed constant throughout
Teaser label
IndustryContent type
BlogsPublish date
10/28/2025
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
Similar jobs at ICON
Salary
Location
United States of America
Location
Multiple US Locations
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
This role involves supporting the execution of clinical trials by managing administrative tasks and monitoring trial progress. The position is responsible for coordinating and tracking all study docum
Reference
JR139022
Expiry date
01/01/0001
Author
Kala MurphyAuthor
Kala MurphySalary
Location
Japan, Tokyo
Location
Tokyo
Remote Working
Office or Home
Business Area
ICON Strategic Solutions
Job Categories
Corporate Support
Job Type
Permanent
Description
【職務内容】弊社のFSP部門(Functional Service Provider)における外部就労案件にてBusiness Operations Manager – Site Contracting(弊社タイトルManager, Contracts想定)として下記ご担当いただきます。※ご経験によっては、Business Operations Associate - Site Contracti
Reference
JR137772
Expiry date
01/01/0001
Author
Mai TakanashiAuthor
Mai TakanashiSalary
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
Medical & Scientific Affairs
Job Type
Temporary Employee
Description
We are currently seeking an Environmental, Health & Safety (EHS) Manager to join our diverse and dynamic team. As an EHS Manager at ICON, you will play a pivotal role in ensuring the safety and well-b
Reference
JR139106
Expiry date
01/01/0001
Author
Hanna PitcairnAuthor
Hanna PitcairnSalary
Location
Mexico, Mexico City
Department
Full Service - Medical Affairs & Pharmacovigilance
Location
Mexico City
Sofia
Warsaw
Remote Working
Office or Home
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Operations
Pharmacovigilance & Patient Safety
Job Type
Permanent
Description
What you will be doing: Conduct comprehensive reviews of clinical trial protocols, patient records, and medical documentation to ensure compliance with study protocols and regulatory requirements.Coll
Reference
JR138500
Expiry date
01/01/0001
Author
Florencia PistolesiAuthor
Florencia PistolesiSalary
Location
Brazil, Sao Paulo
Location
Sao Paulo
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
We are currently seeking a Clinical Research Associate to join our diverse and dynamic team at ICON Plc. As a key member of our research department, you will be responsible for overseeing and coordina
Reference
JR138529
Expiry date
01/01/0001
Author
Bruna DuarteAuthor
Bruna DuarteSalary
Location
Mexico, Mexico City
Location
Mexico City
Remote Working
Office Based
Business Area
ICON Full Service & Corporate Support
Job Categories
Regulatory Affairs
Job Type
Permanent
Description
Senior Regulatory TechnicianLocation: Mexico City only – Office based role (Hybrid)As a Senior Regulatory Technician you will work with the Clinical Trials Information System (CTIS), and will also
Reference
JR134308
Expiry date
01/01/0001
Author
Elizabeth DaviesAuthor
Elizabeth Davies