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Contracts Documentation Specialist

Spectraforce Technologies
United States, Illinois, North Chicago
Aug 13, 2025
Position Title: Contracts Documentation Specialist

Work Location: North Chicago, IL 60064

Assignment Duration: One year with possible extensions

Work Schedule: Monday-Friday, 8:00 AM-5:00 PM

Work Arrangement: Hybrid Onsite Schedule (Remote on Monday and Friday; onsite Tuesday-Thursday)

Position Summary:

* Responsible for maintaining essential contract documents/data in the contract database to be in compliance with corporate policies.

Background & Context:

* Team of 15 manages the clinical payment process for all clinical trial vendors and sites. Role is vendor-focused, managing invoice issues for sites and vendors. Conducts financial reconciliation when studies close to ensure all payments are processed and POs are closed.

Qualification & Experience:

* High School diploma or equivalent with minimum of 5 years relevant experience or an Associate's Degree with 2 years relevant experience or a Bachelor's Degree with a minimum of 1 year of relevant experience.

* Strong math, communication skills and experience with MS Excel and database entry necessary. Prefer experience in clinical research, Finance, Outsourcing, Accounts Payable or equivalent.

* Strong knowledge of standard business procedures including contracting, finance, and budgeting.

* Demonstrated ability to manage projects to completion within deadlines. Demonstrates analytical and critical thinking skills.

* Operates independently and with minimal oversight.

* Strong understanding of the overall Global Clinical Study process is preferred; knowledge of a clinical study protocol and ability to translate it into contractual payment terms.

* Must be proficient in Microsoft Office and able to learn new software/technology quickly; knowledge of SAP, RAVE Electronic Data Capture, MIDAS, Quantum, Qlik, COMPASS preferred.

* Must have attention to detail and the ability to recognize and work with manager to resolve computational and contractual errors.

* Well-developed communication skills and effective interaction with professionals, external sites, and vendors.

Key Responsibilities:

* Responsible for compliance with applicable Corporate & Divisional Policies & procedures. Demonstrates operational knowledge of the applicable SOPs & practices required to effectively process clinical contracts.

* Responsible for the audit and financial reconciliation of clinical study trial vendor contracts utilizing various financial systems to summarize and consolidate payment history.

* Performs ongoing contract entry for all executed contracts.

* Primary interface with Clinical teams and other functional groups for payment-related activities. Assisting in the identification of payment discrepancies and propose resolutions and strategies to avoid them in the future.

* Coordinate payment timelines between Payment Specialists and other functional areas.

* Uses available databases and resources related to EDC database(s) in order to set-up payments in departmental database / system; May enter contract data into departmental database / system.

* Communicate status to management including proposing recommendations for issue resolution.

* Responsible for producing accurate and high-quality payments and reports in a timely manner.

* Investigate and resolve issues that arise independently or with minimal oversight.

* Coordinates clinical trial payments ensuring payments are properly processed within specified timelines including timely distribution of incoming invoices and tracking into appropriate databases.

* Provides guidance/information & answers to technical & non-technical questions regarding contracting process.

* Requisition processing of vendor agreements and Clinical Study Agreements (CSA) into contracting database, including a solid understanding of any auditable documentation needed for payment processing.

* Recognize & resolve vendor management issues to maintain system integrity.

* Processing of monthly electronic data capture (EDC) invoices for CSAs operating in trials.

* Verification of patient activity performed for each agreement when processing invoices.

* Independently investigate and resolve clinical trial vendor or site payment disputes.
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