PRAHS

Senior Investigator Pricing Analyst

Posted Date 7 hours ago(6/20/2025 10:48 AM)
ID
2025-120246

Overview

As a Senior Investigator Pricing Analyst, you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

Responsibilities

General Description:

 

Senior Investigator Payment Associate 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.

 

Qualifications

  • Bachelor’s (BA/BS) Degree from accredited college or university
  • At least 2 years of 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.

Our benefits examples include:

  • Various annual leave entitlements
  • A range of health insurance offerings to suit you and your family’s needs
  • Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead
  • Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being
  • Life assurance
  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others


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