SPONSORS

SIGMA Clinical Research Group collaborates with biotech, pharma and Clinical Research Organization (CRO) stakeholders to execute the clinical trials at our research sites.

We assist Sponsors/CROs in finding qualified sites, study delivery teams and diverse trial participants. 

We offer Sponsors/CROs solutions to find the right study participants and recruit them with high retention rates in trials while meeting study milestones within budget and timeline.

We adhere stringently to all ICH-GCP guidelines, Health Canada and FDA regulations, and study protocols to conduct clinical trials with integrity and accuracy.

We combine our scientific and operational expertise to execute excellence for each project. Our leadership team provides study management and quality assurance throughout the study.

Our team consists of an active, board-certified principal investigator either in solo practice or well-established group practices. 

Here are the benefits of choosing our services:

• Rapid Study Start-Up process including feasibility, budgeting, contract negotiations, questionnaires, and IRB submissions

• Independent clinical research site

• Highly trained and experienced staff

• Physician with hospital privileges

• Quality Assurance department

• Bilingual staff members

• Full-time recruitment and retention department with community outreach, physician practice outreach, digital, social, and media campaigns, a large internal EMR database system, and transportation provided for patients in need.