Investigator Payment Associate
- India
- Clinical Trial Support
- ICON Strategic Solutions
- Remote
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Senior Talent Acquisition Business Partner
- Icon Strategic Solutions
About the role
The Payment Administrator (PA) plays an important role in driving the calculation of payables to investigators and sites in clinical trials and for managing and overseeing payment processes based on site contracts and CTMS data ensuring compliant practices. PA will be responsible for timely and accurate payouts.
The role involves close interaction with key internal stakeholders to provide a seamless and secure financial experience.
Responsibilities:
- Create/Review Site Payables Tracker containing study- and site-specific fee schedule framework (consistent in all countries) and review with Country Budget Developer
- Extract data listings from EDC (RAVE)
- Calculate payables per study site as per negotiated budget/fee schedule.
- Maintain payables in central tracker/repository.
- Liaise with Local Study Team Contact to provide calculation of payables and to discuss any findings, if applicable
- Liaise with Country Budget Developer and Site Negotiator to review any amendments with regards to site data and payables
- Review milestones/study status in VCV and with Local Study Team Contact and align payment schedule/payable process as applicable.
- Ensure payables are only processed based on fully signed contracts/amendments.
- Conduct periodic review of payables in repository and escalate any issues/concerns to relevant stakeholders.
- Review and reconcile payments/payables at site close-out and confirm balance to Local Study Team Contact
- Ensure compliance with company’s Code of Conduct and company policies and procedures relating to people, finance, technology and security.
Essential Qualifications:
- College or Bachelor degree in business related discipline, preferably in computer science or finance, or equivalent qualification that supports skills and capabilities of the position and ensures successful conduct of responsibilities and appropriate interactions with internal and external customers.
- Experience in a clinical trial environment and sound knowledge in managing payments to Clinical Trial Sites / HCP / HCO
- Proven SAP user experience.
- Well-developed Excel skills and basic mathematical skills
- Highly developed analytical skills and excellent problem-solving skills
- Ability to develop advance computer skills to increase efficiency in day-to-day tasks.
- Excellent attention to details.
- Proven organizational and administrative skills.
- Ability to multi-task in a high-volume environment with shifting priorities.
- Ability to work in an environment of remote collaborators.
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
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Teaser label
A Day In The LifeContent type
BlogsPublish date
04/21/2023
Summary
From Clinical Trial Assistant to Clinical Operations Manager, Adrienne Purdy shares her journey.Tell us about you role and what you do at ICON? I have been at ICON since 2013 and I have been growing
by
Adrienne Purdy

Teaser label
Inside ICONContent type
BlogsPublish date
01/26/2023
Summary
The CRO market has seen an unmistakable uplift in demand for its services in recent years. The call for personalised medicine, pricing pressures, and increasing complexity in clinical trials are j
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Teaser label
Inside ICONContent type
BlogsPublish date
10/03/2022
Summary
In traditional clinical trials, patients must attend regular check-ins at hospitals or clinics but fully remote decentralised clinical trials (DCTs) and hybrid trials limit this by replacing the in-pe
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