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Posted: Thu Apr 05, 2007 8:36 pm Post subject: US-MA-Canton: Clinical Research Associate I |
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Date: 05-Apr-2007
Clinical Research Associate I
Job Details:
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Perform tasks to support Clinical Affairs staff and clinical trial
management function including: · Develop/manage Clinical trial
tracking and reporting systems/tools/technologies (i.e. regulatory
documents, CRF, lab sample, enrollment, financial, PO and site
payment) · Create/prepare reports, coordinate/organize departments
records · Assist in preparation of contracts, reports, and
correspondence · Maintain current Clinical Affairs databases · Support
contact for clinical investigative sites · Create and maintain study
manual documents as needed · Support Clinical Research Associates as
needed · Refine/maintain and audit clinical central file system ·
Manage clinical supply order process while also filling order requests
· Plan/coordinate/support clinical off site meetings and arrange
travel as needed · Participate in project specific meetings · Provide
Regulatory submission support as needed · Regulatory document
collection/review · Maintaining dept. calendars and perform minor
administrative duties as needed
Education and Experience: · Previous experience of at least 1-2 years
in clinical research and/or industry preferred · B.S. in a scientific
discipline; Medical device experience a plus · Strong organizational,
interpersonal and communication skills · Working knowledge of GCP/ICH/
CFR regulations for conduct of clinical trials a plus · Ability to
handle multiple tasks and projects simultaneously · Experience with
Microsoft Word, Excel, Access, PowerPoint and Outlook.
Thank you,
BioTech FYI Center
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