PAS Research is excited to announce we have expanded! We are now offering Site Management Organization services! With over 40 years combined Clinical Trial Experience we will provide clinical trial related services to other contract research organizations, pharmaceutical companies, biotechnology companies, medical device manufacturers and clinical sites.
This includes operational, Qualified Research Professionals (CRC, CRP), regulatory and other centralized research support services for research naive and research experienced sites at no cost to you.
SMO Overview
PAS Research Site Management Organization (SMO) offers operational, regulatory and other research support services for sites on industry-sponsored and investigator-initiated trials. With access to a diverse PI base, the SMO supports from Cohort/Observational, Phase 1 through 4 and outcome studies.
Our services include:
- Complete study management from feasibility through closeout
- Efficient and rapid study initiation
- Technology integration and Support
- Contract and Financial services which includes budget negotiations
- IRB management
- Good Clinical Practices (GCP) Training and review
- Qualified Research Professionals on Site
- Subject Safety Management
- Develop relationships with Pharmaceutical Companies, CROs, Biotechnology Companies, Medical Device Manufacturers on behalf of the site
- Subject identification
- Subject recruitment and retention management
- Informed Consent
Study Document completion and timely submission
The great news is you don’t need any previous research experience! Let our combined over 40 years of clinical trial experience be behind you. Fill out the form below to get started.