The Site Payment Analyst ensures investigational site payments and subject reimbursements are made in accordance with Clinical Trial Agreements, reimbursement plans and regulations.
Joins ICON plc, a leading clinical research organisation powered by healthcare intelligence.
Responsible for entering Investigational Site Budgets into the site payment system and performing QC and reconciliation reviews.
Release payments as outlined in Investigational Site Clinical Trial Agreements.
Acts as a point of contact for investigational sites for questions related to payments
Requirements
Minimum of 2 plus years of related experience
Experience with PC-Windows, word processing, and electronic spreadsheets required.
Knowledge of ICH and local regulatory authority drug research and development regulations required.
Clinical trials support or pharmaceutical industry experience required.