Clinical Trials and Medical Research Studies in Columbus Ohio

Clinical Research Coordinators

A Clinical Research Coordinator is responsible for conducting clinical trials using Good Clinical Practice (GCP). They are monitored by an Institutional Review Board (IRB ) and are under the supervision of the Principal Investigator (PI)

The Staff at Columbus Clinical Research works off of four key elements;

• Integrity : every coordinator and the PI place the volunteer first above everything else. We are responsible for answering all of the patient’s questions and concerns and are there whenever the patient has a problem.
• Service : We pride ourselves on having volunteers that return for other studies and refer other volunteers. We think of ourselves as a family and treat patients as we would like to be treated.
• Dedication : Every staff member at CCR is committed to giving 100% to every study and volunteer. We strive to be number one in every aspect of research and to help within the medical community.
• Communication : The staff at CCR are dedicated to providing all volunteers with thorough information of all studies start to finish.

Dr. Samir Arora

Dr. Arora went to medical school in Manipal, India. He then did his residency at Hamot Medical Center in Erie PA. During his residency he worked on multiple original research studies one of those on breast feeding received national attention garnering interviews on major networks and newspapers. Since then Dr. Arora has been involved in clinical research acting as principle investigator or sub investigator on over 100 studies. He holds the prestigious CPI designation by the ACRP. He is the president and medical director of Columbus Clinical Research and is actively involved in the running of the company.

Amanda Reeves

Site Operations Manager
614-501-6164 ext 2006

Amanda has 10 years research experience. She is CCRC certified and is also a member of SOCRA. Her responsibilities include oversight of all office activities, Regulatory Start up and Completion, Budget and Contract Negotiation, and Business Development.

Clinical Research Assistants:

Our Clinical Research Assistants help our Coordinators with the activities of each study. Their duties may include, Blood Draws, ECG, Sample Processing, and Data Entry. All Research Assistants are IATA certified as well as GCP trained.

Recruitment Coordinators:

Our dedicated team of recruitment coordinators work hard at pre-screening and screening patients, making sure that they are the right fit for our enrolling studies.

Clinical Research Coordinators

Our Clinical Research Coordinators are responsible for the organization, coordination, and overall integrity of the trials that we participate in. Their responsibilities include Obtaining participant informed consent, Scheduling tests and procedures, Collection of clinical research data, and Ensuring accuracy of documentation.