Welcome to

Sigma Clinical LLC

Is a Boutique Research Company that
provides Clinical Trial Services.

Reliable and High Quality Clinical Trial Services

About Sigma Clinical

Whether it’s project management, clinical monitoring, protocol development, patient recruitment, data management, or regulatory compliance, we handle every aspect of clinical research with the highest standards of excellence.

we are partners in providing timely and cost effective clinical trial services.

Our Services

Work Area

Choosing the right site is critical to the success of a clinical trial. At Sigma Clinical LLC, we conduct comprehensive feasibility assessments to identify the most suitable locations based on investigator expertise, patient demographics, site infrastructure, and regulatory readiness. Our data-driven approach ensures trials are placed at high-performing sites with proven track records, optimizing patient recruitment, retention, and compliance. By leveraging our extensive network of research sites and healthcare institutions, we reduce delays and enhance the efficiency of clinical studies.

We provide end-to-end site management to ensure clinical trials run smoothly, efficiently, and in full compliance with regulatory requirements. Our dedicated team coordinates with investigators, site staff, and sponsors, handling all aspects of site activation, protocol training, and regulatory documentation. We proactively address challenges related to patient enrollment, protocol deviations, and operational bottlenecks, ensuring that each site maintains high-quality standards throughout the study. With a centralized communication system, we streamline processes and minimize administrative burdens on research teams.

Maintaining the integrity and accuracy of clinical trial data is essential. Our on-site and remote monitoring services ensure that studies adhere to protocols, regulatory guidelines, and ethical standards. We conduct regular site visits, source data verification (SDV), and risk assessments to detect any discrepancies or compliance issues early. Our team works closely with investigators to ensure patient safety, accurate documentation, and efficient trial execution. Through our real-time reporting system, we provide sponsors with transparent insights into study progress, allowing for timely decision-making.

With advances in clinical trial methodologies, a risk-based approach to monitoring is crucial for efficiency and cost-effectiveness. At Sigma Clinical LLC, we implement centralized data analytics to identify high-risk sites, critical data points, and potential deviations before they become significant issues. By focusing on key risk indicators, we optimize resource allocation, reducing the need for excessive on-site visits while maintaining data integrity and regulatory compliance. Our strategy ensures faster issue resolution, improved patient safety, and enhanced trial efficiency, making the monitoring process more adaptive and responsive.

We create detailed, regulatory-compliant study protocols that align with industry standards and scientific best practices. Our team collaborates closely with sponsors to ensure study objectives, methodology, and endpoints are clearly defined. With a focus on efficiency and accuracy, we optimize trial designs for seamless execution and reliable results.
Finding the right participants is critical to the success of any clinical trial. We leverage advanced screening methods, digital outreach, and investigator networks to recruit diverse and eligible patients. Our retention strategies ensure long-term engagement, reducing dropout rates while maintaining the integrity of study data.
Our team ensures the highest quality data collection, validation, and analysis throughout the clinical trial process. Using advanced electronic data capture (EDC) systems and rigorous monitoring techniques, we deliver precise, real-time insights that help accelerate drug and treatment development with confidence.
Navigating the complex landscape of clinical trial regulations is our expertise. We ensure full compliance with FDA, EMA, and ICH-GCP guidelines, handling all regulatory submissions, approvals, and documentation. Our proactive approach mitigates risks, ensuring trials run smoothly while meeting all ethical and legal requirements.

Sigma Clinical are Experts in

Expertise

Project Management

Clinical Trial Management

Clinical Study Management

Clinical Monitoring

Quality Assurance & Compliance

Team Members

Our Team
team-member-1
Dr. Martin Tompson
PHD Student
team-member-2
Dr. Milford Runolf
PHD Student
team-member-3
Dr. Clarabelle Samber
PHD Student
team-member-4
Dr. Henriette Saterfield
PHD Student

Let us help you to find a SOLUTION that meets your needs.

Contact Us

Have questions about our clinical trial services? Our team is here to provide expert guidance, customized solutions, and seamless support to ensure the success of your research. Whether you need assistance with site selection, trial management, patient recruitment, or regulatory compliance, we are committed to helping you navigate the complexities of clinical research with confidence.

Get in touch today and let us be your trusted partner in advancing medical research.

Fill in the form and contact us!