2013 -2017 TRS Publishing, Viewing and Toolbox Product Manager @
2011 -2013 Electronic Submission Expert @
2002 -2011 Principal Submission Specialist @
2002 -2002 Regulatory Production Specialist @
1999 -2002 Clinical Publisher and Documentation Specialist @
Kim Graf Skills
eCTD
Isi Toolbox
Microsoft Office
NDA
Regulations
SharePoint
Clinical Documents
Regulatory Submissions
Patient Safety
Validation
Manufacturing
Adobe Acrobat
Marketing Strategy
Product Management
Electronic Document Management Systems
Evalidator Tools
Social Media Marketing
IND
Ectdxpress
Coredossier
Document Management
Clinical Research
Social Media
Customer Service
Leadership
Electronic Common Technical Document Ectd
EDRMS
Marketing
Regulatory Affairs
Publishing
u.s. Food and Drug Administration Fda
Computer System Validation
Clinical Trials
Sop
Advertising
GxP
Regulatory Requirements
Standard Operating Procedure Sop
Pharmaceutical Industry
21 CFR Part 11
SOP development
Electronic Common Technical Document
Standard Operating Procedure
u.s. Food and Drug Administration
Kim Graf Summary
Kim Graf, based in Wilmington, DE, US, is currently a Associate Director at Incyte. Kim Graf brings experience from previous roles at Incyte, DXC Technology, CSC and AstraZeneca. With a robust skill set that includes eCTD, Isi Toolbox, Microsoft Office, NDA, Regulations and more. Kim Graf has 3 emails and 1 mobile phone numbers on RocketReach.
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