Clinical Trial Associate - Temporary

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POST DATE 9/8/2016
END DATE 11/2/2016

Raptor Pharmaceuticals Novato, CA

Company
Raptor Pharmaceuticals
Job Classification
Full Time
Company Ref #
360709
AJE Ref #
576116166
Location
Novato, CA
Experience
Entry Level (0 - 2 years)
Job Type
Temporary

JOB DESCRIPTION

APPLY
div class="col-sm-12 col-md-8 col-md-offset-1 col-md-push-3" strong Clinical Trial Associate – Temporary /strong p strong span span span Location:  Novato, CA /span /span /span /strong /p p strong span span span Requisition #: 65-3200-2016C /span /span /span /strong /p p strong span span span Summary Description /span /span /span /strong /p p The Clinical Trial Associate provides clinical trial management support to the study team.  This is a temporary position.   /p p strong span span span Responsibilities /span /span /span   /strong   /p ul style="list-style-type:disc" li Collect, review for accuracy, data enter into CTMS, and file essential documents in the Trial Master File.  /li li Assist in study start up activities including but not limited to review of sample Informed Consents, development of study reference manuals, managing study supplies, and processing Investigator Packages. /li li Provide accurate and up-to-date information and study status reports to the clinical team members by pulling accurate and current reports from the CTMS, maintain in-house electronic and paper storage of clinical document archives and Trial Master Files. /li li Participate in and support planning, conduct, management and completion of studies through interaction with sites, vendors and team members. /li li Serve as central contact of the study team in study-related communications, documentation, and correspondence. /li li Assist in the coordination and organization of clinical meetings such as team meetings, CRO meetings, Investigator Meetings, and Data Safety Monitoring Board (DSMB) meetings as applicable; work in collaboration with event planners and/or event staff to accomplish meeting preparation and execution. /li li Provide suggestions and contribute to implementation of process improvements in support of team, department, and company goals. /li li Proficient in Microsoft Office programs with STRONG skills in Excel spreadsheets/workbooks. /li li Perform other duties in support of Clinical Operations, as requested. /li li Participate in clinical operations project meetings, including scheduling, agendas, minutes, etc. /li /ul p span span span