Are You Experiencing Clinical Research Challenges?
Can you relate to any of the below?
CLINICAL RESEARCH SITES
Are you a clinical trial investigator or site staff member involved in carrying out a clinical research study?
- Have you spent time, effort, and resources to open a trial at your site, only to enroll one or two patients, or none at all?
- Are you drowning in hundreds of queries?
- Are you constantly reporting the same types of violations?
- Could you and/or your colleagues benefit from initial or additional clinical research training?
CROs/PHARMACEUTICAL COMPANIES
Are you a monitor working for a contract research organization or do you work for a pharmaceutical company?
- Do your sites consistently have a delay in data entry?
- Do you have to add additional monitoring visits because there are numerous issues with data collection and reporting, specimen collections, study drug accountability, and the regulatory binder?
- Do you find that there is a lot of missing source documentation?
If you said "YES" to one or more of the above questions, you are not alone.
Whether you’re from a pharmaceutical company, contract research organization (CRO), academic or hospital research center, patient advocacy group, or nonprofit research network, if you’re involved in clinical research, you have faced similar challenges.
As a third-party, independent consultant, I can work with you to create and implement strategies for improved efficiency and data integrity.
Schedule a FREE 30 minute, confidential consultation for an initial situation analysis.
About Me
"I provide innovative, hands on solutions to improve data integrity and minimize delays. Together, we can give patients more treatment options, faster."
Ioanna Tsakos
Founder, clinical research consultant