Anderson & Collins Clinical Research, Inc. is owned, managed and coordinated by clinical research professionals with decades of collective experience in clinical trials, applied clinical medicine, and health care management.
Good Clinical Practices
International quality standard that is provided by International Conference on Harmonisation (ICH), an international body that defines standards, which governments can transpose into regulations for clinical trials involving human subjects.Food & Drug Administration
Agency of the US Department of Health & Human Services, responsible for protecting and promoting public health through the regulation and supervision of food safety, tobacco products, dietary supplements, prescription and over-the-counter pharmaceutical drugs (medications), vaccines, and biopharmaceuticals.Standard Operating Procedures (SOPs)
Official, detailed, written instructions for the management of clinical trials. The SOPs are specific to the company and ensure that the functions and activities of a clinical trial are conducted with consistency and efficiency.Each member of our professional staff brings an important and vital component to our site.
In accordance with Good Clinical Practices (GCPs), Food & Drug Administration (FDA) guidelines and meticulous Standard Operating Procedures (SOPs), our team collaborates to effectively execute all aspects of the clinical trial process from site initiation through the study close out visit.
Principal Investigator
An Investigator is a medical professional, usually a physician, under whose direction an investigational drug is administered or dispensed.A Principal Investigator is also responsible for the overall conduct of the clinical trial at his/her site.
Principal Investigator
Our Principal Investigator has a conveniently located primary care medical practice adjacent to our site. Amid a growing Physician Network, we have access to Sub-Investigators from primary care and multi-specialty practices.
Study Coordinators
A medical professional (RN, Physician, MA, etc.) that works directly with study volunteers in accordance with the study protocol, providing them safety and protection while collecting and managing the study data.Clinical Team
Overseen by our Site Clinical Director, our six study coordinators bring invaluable clinical experience as RNs and MDs to our site. This unique combination of advanced medical degrees and extensive clinical research experience provides our patients and sponsors with an unprecedented professional team ensuring all trials are conducted to the highest standards of safety.
Two laboratory technicians certified in phlebotomy assist our coordinators to facilitate efficiency of study visits.
Our Caring Staff
To support our clinical staff, we have a dedicated patient recruiter, regulatory specialist, community outreach coordinator and administrative personnel to ensure that each step in the trial process is executed in a timely and professional manner.
Just fill out our
brief form.