Clinical Trial Monitoring & Oversight Services
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What We Offer
At WilMar Clinical Consulting, we provide comprehensive and flexible clinical trial monitoring services tailored to meet the evolving needs of pharmaceutical sponsors, CROs, and academic investigators.
Whether you're looking for experienced independent CRAs or complete study oversight support, WilMar delivers expert guidance with a focus on compliance, efficiency, and cost-effectiveness.
Why Choose WilMar?
✔️ Objectivity & GCP Compliance
As an independent partner, our monitors deliver unbiased oversight to ensure protocol adherence and regulatory compliance. Our Lead CRA brings over 28 years of industry experience, and every CRA on our team has a minimum of 5 years of hands-on clinical research expertise.
✔️ Cost-Effective Monitoring Models
We specialize in remote monitoring to streamline operations and reduce travel costs. When on-site visits are required, we utilize a regional monitoring model to minimize travel burden while maintaining quality and continuity.
✔️ End-to-End Study Support
In addition to monitoring, we provide:
- Customized monitoring plans
- Pharmacy/Investigational Product (IP) manuals
- Site initiation visit (SIV) training materials
- eTMF maintenance for multi-center studies
✔️ Scalable Solutions
From limited monitoring to full-service study oversight, WilMar offers customizable services based on the size, complexity, and funding of your study.
✔️ Integrated Technology Access
We collaborate with a software partner to provide affordable, scalable technology solutions, including:
- Electronic Data Capture (EDC)
- eConsent
- eCOA / ePRO
- Clinical Trial Management Systems (CTMS)