ACORN CRO is committed to providing value-driven, quality deliverables to the pharmaceutical and biotechnology industry. Having sole focus and deep experience in oncology, ACORN staff fully understands how to navigate the complex clinical and operational issues associated with successful oncology trial management. The full service team comprised of scientists, doctors, nurses, biostatisticians, business professionals, and strong executive leaders work together to ensure timely delivery of quality trial data.
Our full range of services support Phase I-IV trials and includes:
- Study Design/Protocol Development/Medical Writing
- Medical Oversight by a community-based oncologist
- Project Management
- Site Management and Monitoring
- Regulatory Affairs
- Site Contract Negotiations and Payment Management
- Database Design/Build
- Biostatistics/Data Management
ACORN CRO believes that a successful trial begins with a sound start-up plan that focuses on site selection and timelines for maximum enrollment potential. To address this need we developed our proprietary technology tool, Site Tracking and Recruitment (STAR). STAR automates the site feasibility process by matching investigators from our database of over 700 community and academic sites with trial-specific requirements. This technology combined with ACORN CRO’s site start-up expertise and project leadership provides the foundation needed to achieve trial objectives.
6555 Quince, Suite 400
Memphis, TN 38119
ACORN Research - http://www.acornresearch.net