Clinical Trial Coordinator

Custom Search

Plymouth, MNFull-timePosted Apr 12, 2026

Behavioral Health Market Context

Apply Nowvia Jobilize

Job Description

ternal promotion, they are seeking a Clinical Trial Payments/Clinical Trial Coordinator.This role is a backfill to support an existing team member's growth into a Clinical Research Associate role. The specialist will be crucial in managing clinical trial payments and operating within their Clinical Trial Management System for new in-house projects. This position offers a significant growth opportunity for the right individual.

Your role with the company:
• Clinical Trial Payments (approx. 50% of role):
• Manage and oversee clinical trial payments, which will be a heavy focus for at least the next year.
• Conduct administrative tasks and auditing of payments processed by their third-party vendor, Ledger Run.
• Navigate complex and often inconsistent clinical trial contracts, ensuring accurate and timely payments.
• Address various invoiceable items and ensure consistency across sites.
• Requires a strong understanding of clinical trial nuances; general bookkeeping experience is insufficient.
• CTMS Management (approx. 50% of role):
• Operate and manage activities within the Clinical Trial Management System (CTMS), specifically Simple Trials.
• Perform filing, binder creation, and other essential TMF/CTMS management duties for two new in-house projects (no CRO involvement for U.S. operations).
• Experience with other CTMS systems is valuable and should allow for quick adaptation to Simple Trials.
• General Clinical Trial Assistance:
• Take meeting minutes.
• Provide presentation assistance.
• Contribute to other ad hoc tasks as needed within a small, dynamic team.

Desired Profile:
• Proven experience in clinical trial payments is essential.
• Familiarity and comfort operating within a Clinical Trial Management System (CTMS).
• Ability to work effectively in a fast-paced environment.
• Openness to feedback and a straightforward communication style.
• Strong organizational skills and attention to detail.
• Experience in a healthcare setting is a plus.
• Ability to manage multiple tasks and priorities.

Qualifications

  • Requires a strong understanding of clinical trial nuances; general bookkeeping experience is insufficient

Benefits

    Responsibilities

    • This role is a backfill to support an existing team member's growth into a Clinical Research Associate role
    • The specialist will be crucial in managing clinical trial payments and operating within their Clinical Trial Management System for new in-house projects
    • Manage and oversee clinical trial payments, which will be a heavy focus for at least the next year
    • Conduct administrative tasks and auditing of payments processed by their third-party vendor, Ledger Run
    • Navigate complex and often inconsistent clinical trial contracts, ensuring accurate and timely payments
    • Address various invoiceable items and ensure consistency across sites
    • Operate and manage activities within the Clinical Trial Management System (CTMS), specifically Simple Trials
    • Perform filing, binder creation, and other essential TMF/CTMS management duties for two new in-house projects (no CRO involvement for U.S. operations)
    • Experience with other CTMS systems is valuable and should allow for quick adaptation to Simple Trials
    • Provide presentation assistance
    • Contribute to other ad hoc tasks as needed within a small, dynamic team


    More Jobs