I confirm that I am a U.S. citizen or a non-citizen with permanent resident status. Yes: No: *
I also state my understanding that the Summer Institute can accommodate only a limited number of applicants and that an applicant who fails to attend after acceptance denies another worthy applicant the opportunity to participate. Therefore, I assure the National Institutes of Health that, if accepted, I will participate in the full program and attend all lectures and group sessions of the Summer Institute from 6:00 PM on July 13 to 3:00 PM on July 25, 2008. *
Personal Statement indicating the basis of your interest in the Institute, your research goals, and how the course would be beneficial to your pursuit of those goals. (Two pages maximum, attached as a Word .doc or Acrobat .pdf file)
Sponsor Letter from someone who is familiar with you and your research. (Two pages maximum, attached as a Word .doc or Acrobat .pdf file. If your sponsor prefers to mail a hard copy, please contact Ms. Monica Duda for further instructions at mduda@blseamon.com or 301-577-0244, ext. 56)
Personal/Contact Information:
Current Address
Your March/April 2008 Address (if different from current address)
Curriculum Vitae: Please provide your CV and insure that it includes the following
List any grants on which you have been listed as a co-investigator or principal investigator. Give the funding agency, the period of support, and the direct costs (not the total or the total direct costs). Provide two separate sections, one for NIH grants, the other for non-NIH grants.
For each research experience you deem relevant, please give a one sentence overview of what the study was about and what methodology was used (e.g., was it a laboratory experiment, an epidemiological analysis, etc. [Report clinical trials experience separately; see next section]; Then, very briefly describe your role(s) on the project, including the duration of your involvement.
If you have had prior experience with clinical trials, please give a brief overview (a couple of sentences) of what the trial(s) was (were) about. Provide the nature of the intervention(s), the control group(s) used, the outcome measures, and the study duration for research participants. Then, very briefly describe your role(s), including the duration of your involvement.
Please describe the resources in your environment that are available to you to aid you in becoming an independent clinical trialist.