Regulatory Affairs Consultant
Location: Wilmington, Delaware
Description: Fladger Associates is presently looking of Regulatory Affairs Consultant right now, this vacancy will be dwelled in Delaware. More complete informations about this vacancy opportunity kindly see the descriptions. Review and facilitate signing of documents including Power of Attorney, Letters of Authorization, etc. by internal and external partners, follow by tracking of notarization/le! galization and shipment.
Track documents throughout the process and resolve issues related to delays or lost requests.
Ensure documents are completed and arrive at affiliates before due dates.
Significant amount of contact with international markets regional leads to clarify requirements, receipt of information, and critical timelines.
Update status of specific projects upon request and debrief on market requests/ needs with project team.
Provide weekly progress reports.
Track project deliverables in SharePoint (excel spreadsheet) and monitor project status.
Responsible for uploading submission documents to SharePoint and ERIS (Electronic Regulatory Information System).
Report directly to Senior Director AP &LA, GRA, and support global regulatory team
B.S. degree in a biologic or chemical discipline.
Basic understanding of drug development process and supply chain.
Prior experience in international regulatory affairs preferre! d.
Proficient in Microsoft Word and Excel.
Good writte! n communication skills.
Attention to details and ability to track and organize a large number of submission documents.
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If you were eligible to this vacancy, please deliver us your resume, with salary requirements and a resume to Fladger Associates.
Interested on this vacancy, just click on the Apply button, you will be redirected to the official website
This vacancy will be started on: Sat, 20 Jul 2013 09:05:09 GMT
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