Clinical Monitoring & Site Management
Talk about a function that has seen significant change over recent years. Gone are the days of 3-part NCR, sticky notes, and manual tracking of patient accrual and progress. Automated systems, electronic medical records, EDC, risk-based monitoring – all have impacted clinical study monitoring. But the basis for monitoring remains the same – ensuring enrollment of qualified patients, protocol compliance, accurate data collection, timely reporting of potential safety issues, and investigational product accountability.
If you are seeking minimally-experienced CRA data-checkers, we’re not your solution. Led by a Director with 30 years of monitoring experience, our network of office- and regionally-based clinical research associates (CRAs) possess broad therapeutic experience and are proficient in and adaptable to a wide variety of systems. All are GCP certified and trained in Peachtree SOPs. Thus, we can provide qualified CRAs in close proximity to your clinical sites ensuring cost effective study site compliance.
Whether you have a full-service clinical program need or require extra CRAs to augment your internal staff, give us a call to discuss your challenge and our flexible, scalable, and reliable solutions.