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1 by trained researchers and confirmed by the principal investigator.
2 ore the age of 51, the average age of an NIH principal investigator.
3 nd regimen received had been provided by the principal investigator.
4 n oncologists; 37%, women; and 83%, research principal investigators.
5 cal trial ($110,869) and multimode ($59,916) principal investigators.
6 ry 1985 through March 1996 and by queries of principal investigators.
7 n binge diaries and reviewed weekly with the principal investigators.
8 ic training and professional profiles of the principal investigators.
9 Science Foundation's recent mandate that all Principal Investigators address the broader impacts of t
10 l, basic, or social science faculty who were principal investigators), amount of annual income receiv
11 n day 1 of each treatment cycle (28 days) by principal investigator and coinvestigators at the site.
12 are described, and a survey was sent to the principal investigator and primary clinical coordinator
13 ts from an NCI-sponsored meeting with MBCCOP principal investigators and data from a follow-up survey
16 easing numbers of new agents, fewer domestic principal investigators, and more companies off-shoring
17 dation (NSF) Biological Sciences Directorate principal investigators (BIO PIs), nearly 90% indicated
19 lusively conducted basic science research as principal investigators compared with translational rese
20 nd nine other publications coauthored by the principal investigator contain at least one major untrue
22 dividual participant data requested from the principal investigator for each eligible trial, adjustin
27 in the context of the author's experience as principal investigator in a large, randomized trial on c
30 n the context of the authors' experiences as principal investigators in the phase I/II and/or phase I
31 ants between 1964 and 2004 stratified by the principal investigators' major degrees (MD, PhD, or MD a
37 participated in our study reported becoming principal investigators on industry clinical trials prim
39 emic, private-sector physicians who serve as principal investigators on US clinical trials sponsored
41 y while 45% (n = 40) required them only from principal investigators or those conducting research.
42 ical researchers (OR, 1.6; 95% CI, 1.1-2.3), principal investigators (OR, 4.3; 95% CI, 2.8-7.0), facu
43 llocation, but allocation was concealed from principal investigators, participants and their guardian
44 b of a research-intensive faculty member and principal investigator (PI) as both unattainable and und
45 ical Pharmacology/Micromedex), or study site principal investigator (PI) opinion-among patients recei
49 Blood Institute-supported publications each principal investigator published in the 5 years before g
50 first draft was written in April 1996 by the principal investigator (S.G.P.) after the consensus grou
51 the role of these authors rather than of the principal investigator(s) as in the previous policy.
54 located to placebo; none were judged by site principal investigators to be related to study medicatio
55 for extensive response and redrafting by the principal investigator until all members were satisfied.
58 total dollar amount of R01 grants awarded to principal investigators with only an MD degree trended d
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