Investigator Payments Specialist (FSP)

Parexel are currently recruiting for an experienced, clinical trial payments specialist/associate who has experience across the EMEA region.

In this position you will be an invaluable ensuring that the processing of invoices and payments to investigators and vendors; reconciling payments with sites, vendors and corporate Finance happens as accurately and efficiently as possible.

Some specifics about this advertised role

• 100% homebased
• Processes approvals and payments for invoices submitted by sites/vendors/clinical research organizations (CROs)
• Ensures payments are within contractual agreements
• Ensures appropriate coding processes are followed for efficiency and consistency
• Identifies out of balance accounting records and reconciles with site/vendor/CRO and the finance department
• Communicates directly with the site and vendors to resolve invoice differences
• Conducts Quality Control process reviews and remediates, as needed
• Maintains the clinical financial database

Who are Parexel

Parexel supports clinical studies across the full range of therapeutic areas, and we have longstanding partnerships with a vast client base.

We supported the trials of most of today’s top 50 best-selling drugs, but equally we enable more niche drug developments that are critical to the well-being of many patients.

You’ll be an influential member of the wider team.

What we are looking for in the this role

For every role, we look for professionals who have the determination and courage always to put patient well-being first.

That to us is working with heart.

Here are a few requirements specific to this advertised role.

• Four (4) or more years of financial experience including Accounts Payable and Accounts Receivable or related experience in a biotech, CRO, finance and/or legal environment
• Experience with financial analysis preferred
• Knowledge of Code of Federal Regulations (CFR) preferred
• Knowledge of Good Clinical Practice (GCP)/International Council on Harmonization (ICH), and European Clinical Trial Directive preferred

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