US-MA: Boston-Clinical Trials Associate

**************************************************************
JobCircle.com is a regional job board serving all industries
and occupations in the PA, NJ, DE, NY, MD, and DC areas.

We offer a regional job board, online learning, and regional
job fair events for jobseekers who live in our areas of focus.

To Learn More:

Job Board: http://www.JobCircle.com?source=ng
eLearning: http://www.JobCircle.com/courseware?source=ng
Job Fairs: http://JobCircleJobFairs.com?source=ng

**************************************************************

Job Title: Clinical Trials Associate
Job Location: MA: Boston
Pay Rate: Open
Job Length: full time
Start Date: 2008-02-05

Company Name: The Cambridge Group Ltd.
Contact: Stephanie Oscar
Phone: E-mail or fax only
Fax: 203-226-3856

Description: Clinical Trials Associate

The Clinical Trials Associate assists the Clinical Project Managers in the conduct of trials and may be responsible for managing startup activities, vendor communication or other project activities as assigned. Responsibilities include: assists with preparation of all external and internal documentation, for assigned trials, to ensure such documentation is completed in accordance with GCP regulatory requirements and is consistent with the study protocol, under close supervision; assists Clinical Project Manager in site management activities which could include review of monitoring report, tracking of site visits, communication with monitors and sites, and other activities as assigned; maintains and tracks revisions to all documentation for accuracy, including patient Informed Consent Forms and Case Report Forms; assists the Clinical Project Manager in ensuring compliance with Clinical Study Protocol and provides timely updates to assigned Clinical Project Manager to confirm compliance; organizes and prepares study files related to study tracking and reporting and submits them to the Trial Master File within established guidelines; may participate in the training of CRO teams, investigators and staff as needed regarding assigned logistics of the clinical trial; tracks delivery and receipt of required supplies and materials to study sites and provides regular status updates. Qualifications include: a B.S. (or equivalent experience); 1 – 4 years of relevant work experience; a working knowledge of ICH GCP regulations and clinical protocols; the ability to ‘multi-task’ effectively; ability to interact well with various team members and provide value added support to projects; and displays ability to independently solve routine problems following standard policies/procedures

Please refer to Job code BG5281 when responding to this ad.


For FASTEST PROCESSING of your resume, please visit http://www.jobcircle.com/classifieds/1112041.html?source=ng to apply online.


**************************************************************
For fastest processing of your resume, this employer asks that
you apply to this job using the URL above.
**************************************************************