Site Services

Regulatory Services

Our Regulatory Affairs team manages all essential documentation and compliance processes to ensure your study is audit-ready and fully aligned with ethical and regulatory expectations. We handle submissions to Institutional Review Boards (IRBs), maintain complete and organized regulatory binders, and manage informed consent documentation in accordance with federal guidelines. All regulatory activities are conducted in compliance with ICH-GCP and U.S. FDA requirements, ensuring accuracy, transparency, and integrity throughout the trial lifecycle.

Finance and Contracting Services

Our dedicated Finance and Contracting team streamlines the financial and legal aspects of your clinical trial. We work closely with sponsors and CROs to negotiate fair and transparent study budgets, ensuring alignment with your site’s needs and resources. Our experts handle timely contract preparation, review, and execution to minimize delays in study start-up. With a focus on compliance and accuracy, our services help investigators and sites maintain financial integrity while supporting smooth trial operations.

Patient Outreach Services

Our Patient Outreach team is dedicated to using morally sound and successful engagement techniques to connect qualified volunteers with clinical trials. To guarantee the recruitment of diversified and appropriate participants, we employ pre-screening procedures, educational programs, and focused community outreach. Our objective is to enhance retention throughout the study and enable informed participation.

Join a Trial with Confidence

At Saturn Research Solutions, we strive to make clinical research a positive and rewarding journey for every patient. Reach out to learn how we can support you in accessing innovative treatments while prioritizing your health and comfort.

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