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CLINICAL INQUEST CENTER Ltd.
Press Releases:

* Clinical Inquest Center Ltd., a Site Management Organization, launches complete array of services to accomplish Clinical Research Studies in the field of Pain Management, Family Medicine, Endocrine / Metabolic Diseases, Psychiatry, CNS, Women's Diseases, Muscular Skeletal, Healthy Patients, PK studies and Ophthalmology. The list is growing fast

Dr Rameswar Chaudhuri a well known Internist joins CIC as an investigator.

* CIC is pleased to launch its new site in Centerville OH. This site will cater to the patient population from Springboro, Mason, Cincinnati etc.

* Dr James deCaestecker a well known Surgeon joins CIC as an investigator

* Dr Jennifer Cova, DO joins the Clinical Inquest Center's Network as a Principal Investigator. She provides complete care for women and is a renowned OBGYN physician in the area. We all welcome her to our team.

* Dr. Daniel Whitmer, a board certified family physician joins CIC team. He has over two decades of experience in conducting clinical trials and will be a great asset to our team.

* Dr. Deepak Sarwal, MD an internist and diabetologist joins our research team as an investigator. His expertise and research experience is a great asset to CIC. We welcome him to our team.

* Dr William Kessler, MD an Ophthalmologist
, joins our research team as an investigator .

* Dr. Avni Arora, MD a board certified Anesthesiologist and Pain management physician joins as an Investigator. She has a wide spectrum of experience in the field of Clinical Research with numerous projects under her belt..

* Two Thumbs up to the CIC's commitment of Best team of Research Coordinators and Regulatory Staff.
Services for Investigators and Sites:

Being a physician and managing your practice and time has been one of greatest challenge. Needless to say that the challenges are extensive be it a solo or group practice. We at CIC understand and appreciate this fully. Therefore we at CIC excel beyond the expectations of a SMO. We expect and strive for the fact that you will do the same tasks in clinical trials as you do in treating your patients. Our list of services to you can be tailored to your needs and is not limited to the following:

Compile all necessary material including CV's, Licenses, patient demographics, research experiecne to MARKET THE SERVICES OF THE SITE and/or INVESTIGATOR ACQUIRE CLINICAL STUDIES FOR THE SITE and/or INVESTIGATORS PROVIDE COMPLETE MANAGEMENT OF THE STUDY
Enable RESEARCH COORDINATORS as per SCHEDULE CONVENIENT TO YOU PROVIDE REGULATORY STAFFf to make sure we cover whole nine yards To avoid duplication of work, utilize the services of our ADMINISTRATIVE STAFF as and when needed
Our MANAGEMENT STAFF is just a phone call away and will respond with 1 business day We take the responsibility of filling all regulatory PAPER WORK and ADMINISTER the clinical STUDY We will also help to oversee your medical practice to allow COST EFFECTIVENESS of the study
Our QUALITY ASSURANCE TEAM will make sure that every aspect of the study has been accomplished correctly utilizing the Standard Operating procedures Finally you will enhance your skills, knowledge and Professional Career and increase revenue of your SITE / PRACTICE YES, WE WILL EXCEED your EXPECTATIONS

If all this sounds interesting to you and you are interested in becoming a part of our network, please feel free to contact us.