Is Conducting A Clinical Study of Interest To You?


If you have an interest in clinical research and are considering conducting clinical research studies yourself, CIS offers professional services to get you started.  Our training process ensures you will learn and launch your first clinical study quickly while fully understanding the responsibilities and benefits of being a Principal Investigator (PI):


The Principal Investigator (PI) is the person ultimately responsible for assuring compliance with IRB policies/procedures, DHHS Federal Policy Regulations, and FDA regulations and for the oversight of the clinical study and the informed consent process. Although the PI may delegate duties to members of his/her research team, s/he retains the ultimate responsibility for the conduct of the study.


CIS offers an array of professional services to suit your needs through an affiliate partnership.

  •      -Clinical study training for you and your staff (terminology, expectations, etc.)

          -Good Clinical Practice (GCP) training

          -Standard Operating Procedures (SOP) guidance

          -Regulatory study submissions and tracking

          -Contract and budget negotiations

          -Patient recruitment services – Advertising and identification of suitable study patients

          -Staff resources where needed so your new studies run efficiently

          -Office space at CIS or CIS consultation regarding usage of your own office space 


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