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  • Memphis, TN

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Clinical Trial Assistant

Nesco Resource • Memphis, TN

Posted 28 days ago

Job Snapshot

Full-Time
Experience - 1 to 2 years
Other Great Industries
Other

Job Description

Description: Skills Needed: effective communication (email, oral, and written); time management, customer focus (internal and external), attention to detail, working knowledge of and recent experience with Microsoft programs (Excel, Outlook, Word); working knowledge of and recent experience with scan/print/fax equipment, willingness and ability to maintain strict confidentiality of records, ability to efficiently navigate internet to update and maintain information on public websites.



This position works closely with clinical study managers and clinical operations staff. Knowledge and 1-2 year(s) experience working in a regulated/clinical environment is required.



Job Duties:

Set up, maintain and archive clinical study master files, provide document management support for clinical study programs, provide general administrative assistance, create and update study/payment trackers, ensure timely processing of invoices and payments, provide check in process for clinical study documents, provide active follow up of outstanding investigational site documents (financial disclosures, clinical trial agreements, etc), maintain ASD clinical trial registrations on clinical trials.gov, and may perform quality assurance/quality control of assigned outputs



Work to be Produced: clinical study files, administrative records and reports, SOPs, legal agreements, payments, registry on clinical trials.gov

Job ID: 19-20719
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