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Regional Clinical Research Associate The Clinical Resource Network has partnered with a growing research organization and is seeking a Clinical Research Associate ...
monitoring pharmaceutical clinical trials. Previous... job tenure within their CRA positions overall and steady progression within the CRA career ladder with the......
monitoring pharmaceutical clinical trials. Previous... job tenure within their CRA positions overall and steady progression within the CRA career ladder with the......
monitoring pharmaceutical clinical trials. Previous... job tenure within their CRA positions overall and steady progression within the CRA career ladder with the......
75% Our Clinical Research Associates manage all aspects of site monitoring responsibilities for Clinical... visits). •3 years clinical research experience in the......
For your reference, we have included the original job posting below.
Clinical Research Associate (CRA)
Job Number:
26706517
Company Name:
Aerotek Scientific
Job Location:
Nashville, TN US
Job Category:
Research
Clinical Research Associate (CRA)
Aerotek is proactively seeking a Clinical Trials Associate (CTA) that will be involved in the conduct of the study and interfaces with the Study Manager and the Study Team. Responsibilities include:- Support to CRO and Regional Operational Lead.- Supporting Clinical Operations and Finance on patient payment timelines, processing, QC and mailing of monthly payment cycles and responding to site inquiries regarding payments. - Support the Study Manager in creating, updating and tracking MS study plans.- Logging, tracking and archival of Regulatory Documents.- Project CTMS Entering Regulatory Files into the Clinical Trial Management System (CTMS) to meet roll-out timelines.- Trial Master File archival and maintenance.- Preparation and coordination of mail merges and mass shipments to sites. - Maintenance of weekly team meeting minutes. - Coordination of study material production.- Prepare and send materials for Site Initiation Visits to sites.- Process drug shipments after gathering necessary essential documents and track the receipt of shipments- Sending/tracking/filing CDAs and sending regulatory packages to new sites.- Maintenance of master study status lists and investigator and trial staff contact information.- Tracking CRFs and queries as appropriate- Distribute and create study documents for the study site such as CDAs, feasibility questionnaires, study binders, etc.- Coordinating distribution of expedited Safety reports and confirming site receipt of those reportsQualifications:- BS Degree- 2+ years of Clinical Trials experience in Pharma/CRO setting Category: Medical Sciences
