RESEARCH CLINICS
SIGMA Clinical Research partners with local physicians in various therapeutic areas, enabling eligible study participants to early access the latest investigational options.
We provide training and guidance for research-naive medical practitioners, helping them get research experience and become productive Principal Investigators (PIs) for industry-sponsored clinical trials.
If any of the following statements apply to you, we are here to help:
1. I want to increase revenue for my practice but don’t know where to start.
2. I have considered starting clinical trials but lack the time to do so.
3. I have faced challenges with clinical studies and need assistance.
Regardless of where you are in your journey, we have the tools and expertise to ensure your success in clinical research. Our proven strategies are designed to make the process as effortless and stress-free as possible.
Our team of experts will work closely with you to find the right study to conduct at your site. We will also help you design a practical and effective clinical research site development plan that aligns with the needs of your practice.
We support clinical trials by placing highly trained SIGMA Direct Delivery Team members (Research Nurses, Clinical Research Coordinators, and Data Coordinators) at each research site to ensure the seamless delivery of the clinical research study with integrity and accuracy.
We offer the following services:
- Establishing Sponsor Network
- Access to New Studies
- Building Clinical Research Site & Site Networks
- Trial Management Training & Certifications
- Development Plan and SOP
- Study Identification and Site Feasibility
- Budget and Contract Negotiations
- Protocol Specific Training
- Site Start-Up
- Marketing and Advertising
- Regulatory Management (HREBA Applications/Approvals)
- Patient Recruitment/Enrollment/Retention
- Investigator Site Files
- Study Documents (ICF/CRF)
- Study Data Management (Data Entry/Query Resolution)
- Safety Data Management (AE & SAE Reporting)
- Monitoring & Audit Visit
- Quality & Compliance
- Invoicing
- Study Close-out
- Query Resolution
- Drug Accountability
- Storage and Archiving
- Training
With our clinical research services, you will be able to:
- Reducing time on administrative work,
- Shortening Study Start-Up timelines,
- Ensuring accurate data collection,
- Reducing data entry time,
- Managing patient biological samples
- Coordinating logistics of the study IP & consumables,
- Ensuring reimbursement of patient expenses and patient logistics,
- Strengthening staff training,
- Ensuring monitoring and audit preparedness,
- Boosting financial results,
- Getting more studies.
If you want to learn more about our services, please don't hesitate to contact us. We'd be happy to work with you directly.
