NEW COURSE - Statistics for Clinical Research
About Us
What is a CRA?
What is a CRC?
Course Demos
Who Should Enroll?
Course Outline
Classroom vs. Online Training
Contact Us
Instructor Bio
Contact Hours
Job Placement Assistance
For MDs Only
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Now is the time to make the job change you want to make!!!


Enroll in our online, self-directed training course, Monitoring Clinical Studies, to become a Clinical Research Associate (CRA), one of the most desireable positions in the pharmaceutical industry. 

See what Money Magazine has to say about the CRA position! http://money.cnn.com/pf/best-jobs/2013/snapshots/9.html

As of  October 15, 2014, one large company (out of many hundreds) is looking for CRAs in the following states: IN, KY, NY, FL, NJ, MI, OH, IL, IO, DE, GA, PA, MD, VA, WV, DC, AZ, MA, CA, HI, NV, UT, OK, CO, KS, NM and TX-and this is just one company. Many jobs available--now. Monitoring Clinical Studies can help you get one of these jobs!!!

$999.99. Includes 3 months' access to Monitoring Clinical Trials, final exam, and job assistance. See "Costs" screen for terms.
                                    Also see our other courses, Statistics for Clinical Trials and Conducting Clinical Trials, described elsewhere on the site. 
                                    Please give us a call if you have any questions or concerns, US toll-free 800-683-6013 or 484-326-4574. Thank you for your business.

  • You will Learn the role & responsibilities of the CRA, Study Site Staff and Sponsor plus the FDA Regulations, International Guidelines (ICH) and Good Clinical Practice (GCP).
  • Why this 50 + hour program is best for you:
    • We provide Job placement assistance when you complete our program. 
    • It will help prepare you for CRA Certification
    • You will participate in many simulations during the training program that will give you "hands-on" experience in actual monitoring situations such as Investigator selection, IRB approval, CRF review, source document verification, drug accountability and adverse event assessment.

Click here to view the "Monitoring Clinical Studies" Course DEMO. When the demo opens, click on the top item in the chart, "Instructions for Use and Introduction," to begin exploring the features and content of the program.


Our alumni include participants from or have taken jobs with Aventis, AstraZeneca, Bayer, Cardinal Health Systems, Cell Therapeutics, Johnson and Johnson, NexGenix Pharmaceuticals, Glaxo, Mednet Solutions, Merck, Novartis, Quintiles, Quest Diagnostics, Ortho-McNeil, Physiomed, Parexel, PPD, Roche, Wyeth and many other small and large companies.


People have taken our courses from the USA, England, Ireland, Korea, Portugal, Puerto Rico, Italy, India, Israel, South Africa, Belgium, Germany, Japan, Netherlands, Australia, Denmark, Switzerland, Canada, Brazil, Kenya, Egypt, Turkey, Austria, Bosnia, Thailand, Argentina, Maylasia, Sweden, Serbia, Singapore, Oman, Austria, Lebanon and Greece.



How to Conduct Clinical Trials---a training program for Clinical Investigators and Clinical Research Coordinators and other Investigational Site personnel.


E-mail ClinicalResearchTrainingOnline@gmail.com for information. Click here to view a DEMO of How to Conduct Clinical Trials  




Once registered for any program you will have access for three months to that training program and the instructor for questions and or discussion. Upon successful completion of any program you will receive a Certificate of Completion.  


Call 484-326-4574 (or toll-free, 1-800 683-6013) to register or discuss any program or have questions answered.  Business hours are 9 am to 6 pm eastern standard time.


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