Senior Investigator Pricing Analyst
- Brazil
- Clinical Monitoring
- ICON Strategic Solutions
TA Business Partner
- Icon Strategic Solutions
About the role
This vacancy has now expired. Please click here to view live vacancies.
As a Senior Investigator Pricing Analyst, you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
What you will be doing:
Senior Investigator Pricing Analyst will undertake activities to provide specialized support and assistance to the Clinical Business Operations and all studies in site payment vendor portfolio. This role partners closely with the Clinical Operations team, contracts and budget team, and site payment vendor. Role will also ensure accuracy and timely site payments for study portfolio by planning, executing, tracking and management of global clinical trial payments.
Experience with site payment vendor management or oversite including holding vendor accountable for services in Statement of Work (SOW).
- Experience creating baseline Investigator Grant budget estimates using a benchmarking tool and assessing for Fair Market Value (FMV)
- Ability to manage total overall study budget as well as global payments, with specific emphasis on the Asia-Pacific region as well as experience with other country specific payment rules and regulations.
- Support the implementation of the SOW and Change Order process and project related cost, if applicable.
- Demonstrated experience in supporting R&D as it relates to Clinical Trial business operations.
- Successfully work with 3rd party site payment vendor resolving site payment discrepancies, historical payment issues, and monthly reporting requests.
- Track payments owed to clinical research sites in accordance with the negotiated unit price per the site Contract.
- Support management in identification of risks, develop mitigation strategies, alternative solutions, resolve issues, action item/follow up in collaboration with cross functional and/or matrix teams.
- Maintain frequent and consistent communication with external partners and/or investigators and internal departments regarding payment activities during the contract lifecycle.
- Able to review Clinical Trial site budgets, if needed.
You are:
- Bachelor’s (BA/BS) Degree from accredited college or university
- Experience on the similar position in clinical research or pharmaceutical industry
What ICON can offer you:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Visit our careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefits
At ICON, diversity, inclusion & belonging are fundamental to our culture and values. Our rich diversity makes us more innovative which helps us better serve our people, patients, customers, and our communities. We're proud of our diverse workforce and the work we’ve done to become a more inclusive organisation. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.
https://careers.iconplc.com/reasonable-accommodations
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.
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
A Day In The LifeContent type
BlogsPublish date
04/05/2023
Summary
Senior Clinical Research Associate Suzaita Hipolito talks about the satisfaction gained from working in Clinical Research. “What would it look like to wake up every day feeling happy and fulfil
by
Suzaita Hipolito
Teaser label
Career ProgressionContent type
BlogsPublish date
03/20/2020
Summary
Navigating the world of graduate schemes and positions can be daunting, especially if you’re not quite sure of the role or company you want to align yourself with. At ICON, we recognise what a s
Similar jobs at ICON
Salary
Location
Hungary, Budapest
Location
Budapest
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
JR146340
Expiry date
01/01/0001
Author
Orsolya BerkeAuthor
Orsolya BerkeSalary
Location
US, Blue Bell (ICON)
Location
Portland
Blue Bell
Los Angeles, CA
Seattle, WA
San Francisco, CA
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
What You Will Be Doing: Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.Conducting site visits to assess sit
Reference
JR140704
Expiry date
01/01/0001
Author
Jonathan HolmesAuthor
Jonathan HolmesSalary
Location
Israel, Tel Aviv
Location
Tel Aviv
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
We are currently seeking a Senior Clinical Research Associate (CRA) to join our sponsor dedicated team. As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical t
Reference
JR146494
Expiry date
01/01/0001
Author
Salome KankiaAuthor
Salome KankiaSalary
Location
Argentina, Buenos Aires
Department
Clinical Monitoring
Location
Buenos Aires
Remote Working
Remote or Office
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
We are currently seeking CRA I / CRA II (Multisponsor & Sponsor Dedicated) to join our diverse and dynamic team. You will play a pivotal role in designing and analyzing clinical trials, interpreting c
Reference
JR140950
Expiry date
01/01/0001
Author
Florencia PistolesiAuthor
Florencia PistolesiSalary
Location
US, Blue Bell (ICON)
Location
Texas
Pennsylvania
Florida
Blue Bell
Chicago, IL
Los Angeles, CA
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
To support 1study in the cardiovascular/electrophysiology medical device space. Indication is A-fib.The ideal candidate will have cardiovascular medical device monitoring experience- however, cardiova
Reference
JR145235
Expiry date
01/01/0001
Author
Monica HawkinsAuthor
Monica HawkinsSalary
Location
US, Blue Bell (ICON)
Location
Massachusetts
North Carolina
Pennsylvania
New Jersey
Blue Bell
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 in the Northeast Region to join our diverse and dynamic team. As a Clinical Research Associate II at ICON, you will play a pivotal role in des
Reference
JR146132
Expiry date
01/01/0001
Author
Jamie PruittAuthor
Jamie Pruitt