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Clinical Trial Associate

Pfizer


Location:
Wuhan R&d Center
Date:
01/26/2018
2018-01-262018-03-02
Pfizer
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Job Details

To provide operational and logistical support to global clinical trial programs in accordance with company SOPs, ICH GCP guidelines and local regulations. To be the primary point of contact where responsibility is held as a Subject Matter Expert for a business system.







+ Provide protocol and ICD administrative support to global Project Managers (PMs) and Study Managers (SMs), including but not limited reviewing protocols, checking the consistency of documents, prepare RighTrack II protocol outputs report, circulate and track the approval status.



+ Request set up of study team SharePoint spaces, grant access to the team and update files in SharePoint for Inspection Readiness documents including team roster changes, , updating version dates etc., and uploading of meeting minutes and any documents to SharePoint as required.



+ Maintain Pfizer Trial Master File (PTMF) in accordance with ICH-GCP and SOPs.



+ File documents to PTMF/ GDMS.



+ Prepare and update the trial and site information as necessary in Corporate Clinical Trial Registry (CCTR) in a timely manner.



+ Assist team with the preparation of any documents upon request, including but not limited to vender oversight plan, correspondence with investigator sites and vendors, study specific manuals for the sites, etc.



+ Track and update all information on an ongoing basis per request, including but not limited to site contact information, required site training attendance, vender information, patient recruitment, trial suppliers, payment schedule, Ariba orders, etc.



+ Attend appropriate training programs and project teleconferences as applicable.



+ Support and coordinate any activities as requested by PMs/SMs and as assigned within required timelines.







Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
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