Clinical Investigators
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Register as a Clinical
Investigator for PRA |
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Click here to fill out the application form.
The information will be transferred to our
Investigator Database.
Investigators will be identified for studies
through a database query process. If you are identified as an
appropriate potential investigator you will receive a call to gauge your
interest in participating in a study from a PRA Clinical Operations
Specialist responsible for site recruitment. The PRA Clinical Operations
Specialist will
be able to answer your questions and concerns about the study and assist
you with regulatory document completion. |
We invite you to join PRA's global investigator database. PRA designs and
conducts Phase I-IV clinical trials for most of the world's leading
pharmaceutical and biotechnology companies, as well as many mid-sized and
emerging companies. We continually seek highly motivated investigational
sites who can consistently meet enrollment quotas and conduct trials to the
highest standards of Good Clinical Practice. To be considered for
participation in our trials, we encourage you to register in our global
investigator database.
Notification of Successful Registration
You will be notified of your successful registration in our global
investigator database and/or contacted to provide additional information.
Selection for Participation on Clinical Trials
Upon award of a new study, our Clinical Operations staff search PRA's
Investigator database for investigators that specialize in the targeted
therapeutic area. We give preference to investigators who met their
enrollment objectives on prior trials. If you are selected during this
preliminary stage, you will be contacted by telephone by one of our staff.
Contact Information
If you have questions or would like to speak with us, please click
here.
Page last updated:
19 June 2008
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