Optimal Research provides clinical site solutions to pharmaceutical and biotech companies, medical device companies, and contract research organizations (CROs) seeking research sites to conduct clinical research studies in a high quality manner. In addition to the six core sites that it owns, Optimal utilizes its oncology and pediatric site network to provide integrated site solutions that meet our client's needs.
Optimal is the intersection where pharmaceutical/biotech companies and patients find excellence in clinical research. Specifically, Optimal provides clinical site infrastructure and staffing to meet the requirements of the clinical trial protocols for men's and women's health, geriatrics, vaccine, oncology, and pediatric health conditions.
Depending upon Optimal’s engagement, its services may include some of the following:
- Protocol / Operations Consultancy
- Site Identification
- Site Contracting
- IRB Submission (Preparation and/or Management)
- Patient Recruitment
- Study Conduct
- Patient Follow-Up
- Trial-related documents archival and maintenance
- Reporting serious adverse events to the Sponsor or CRO
- Ensuring protocol compliance
- Site Training
- Quality Assurance
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