Zurich Insurance Company Ltd
Underwriting Service Specialist
Zurich North America
Underwriting Service Specialist
Kemper Sep 1988 - Dec 1999
Underwriting Assistant
Skills:
Microsoft Office Microsoft Excel Property and Casualty Insurance Insurance General Insurance Reinsurance Customer Service
Ghd
Civil and Environmental Engineer
North American Wetland Engineering 2005 - 2010
Civil and Environmental Engineer
Gannett Fleming 2005 - 2010
Civil and Environmental Engineer
Education:
University of Minnesota 2008 - 2010
Master of Science, Masters, Architecture, Design
Penn State University 1997 - 2002
Bachelors, Bachelor of Science, Civil Engineering
University of Minnesota - Twin Cities
B&H Consulting Services Jul 2016 - Jan 2017
Regulatory Ectd Project Manager
Five Eleven Pharma Dec 2015 - May 2016
Cra and Investigational New Drug Specialist
Accenture Jun 2013 - Aug 2015
Senior Associate, Regulatory Affairs
Merck Apr 2008 - Jul 2009
Patient Informed Consent Specialist
Inc Research Nov 2007 - Jan 2008
Regulatory Specialist
Education:
Temple University 2007 - 2009
Master of Science, Masters
West Chester University of Pennsylvania 2004
Bachelors, Bachelor of Arts, Bachelor of Science
West Chester University of Pennsylvania 1999 - 2004
Bachelors, Bachelor of Science, Business Administration, Management, Business Administration and Management
Skills:
Quality Management Writing Snda Clinical Trials Close Attention To Detail Consulting Internet Backbone Market Ich Gcp Adobe Acrobat Adobe Contribute Overseeing Draft Vendors Sales Location Computing Clinical Reporting Viewpoint Infectious Diseases Clinical Research Converting Ctms Biotechnology Regulatory Affairs Change Control Immunology Data Formats Structure Recognizing Docs Executive Positions Protocol Nda Bioprocess Clinical Monitoring Cross Functional Team Leadership Clinical Development Legal Regulatory Compliance Organizational Structure Databases Edoc Trend C Level Cmc Regulatory Agencies Management Design Contractors Cfr Viewer Therapeutic Areas Hypertext Guiding Hiv Sop Crm 21 Cfr Part 11 Electronic Submissions Leadership Auditing Data Storage Coordinated Clinical Practices Powerpoint Monitors 21 Cfr Requirements Analysis Liaising Affiliation Paperless Pennsylvania Formulate Informed Consent Detail Oriented Gmp Philadelphia Migrating Guidance Full Circle Regulatory Documentation Legal Writing System Cell Super User Project Tracking Virology Project Leadership Publishing Boosting Engineering Reports Asset Allocation Strategy Walkthroughs Strategies Microsoft Office Xml Oncology Microsoft Excel Gcp Drug Development Illustration Training Approval Process Policy Bioethics Testing New Hire Training Ms Project Control Software Patient Editing Certified Financial Planner Disaster Recovery Demonstration Regulatory Submissions Pics Subject Matter Expert Teamwork Business Management Streamline Project Management Documentation Streamlining Research Quality Control Informatics System Monitoring Trains and Add Rails Stakeholders Task Force Investigation Information Management R&D Analysis Written Ind Document Review Biopharmaceuticals Raps Consultancy Services .Net Verizon Promotional Strategy Implementation Trials Multi Functional Instrumental Multiple Locations Space Management System Ectd Fix Protocol Tissue Cognos Accountability Applications Hipaa Communication Schedules Negotiation Radiopharmaceuticals Life Sciences Clinical Research Associates European Union Operational Activities Quality Assurance Good Clinical Practice Anti Inflammatory Safety Regulatory Requirements Author Icf Repository Marketing Edrms New Hires Queries Document Management Time Management Critical Thinking Timelines Pharmaceutical Project Management Microsoft Project Project Planning Documentum Docubridge Project Medical Imaging Pharmacy Consent Data Migration Electronic Document Eager Paper Presentations Batch Records Conforming Case Report Forms Highly Accomplished Internal Audit Manage Multiple Regulations Regenerative Design Cro Obtain Track Record of Success Efficient Establish Priorities Executive Management Patient Recruitment Regulatory Operations Multi Tasking Start Ups Forms Irb Boost Regulatory Reviews Electronics Ich Guidelines Spreadsheets Regulatory Standards Guidelines Process Improvement Bonus Bridge Inspection Legal Advice Qumas Software Medical Devices Sas Oracle Firstdoc Compliance Linking Exploratory Product Lifecycle Management Readable Frame Annual Reports Microsoft Word Program Management Advisement Parties Pharmaceutics Manufacturing Libraries Biologics Marking Vaccines Pharmacoeconomics Endnote Switching Staff Development Risk Pharmaceutical Industry Problem Solving Pre Approval Binders Amendments Emea Fda Recruiting Anticipation Dosimetry Coordinate Pdf
Interests:
Research and Development Equine Animal Health Health Animal Health Drug Development Clinical Research Regulatory Affairs Education Immunology Environment Science and Technology Biomedical Devices Irb Submission Human Rights Bla Tissue Engineering See 6 Nda Civil Rights and Social Action Oncology Small Business Strategy Poverty Alleviation Disaster and Humanitarian Relief Vaccines Business Strategy Business Management Management Strategy Project Management Economic Empowerment Combination Devices Informed Consent Form See Less Animal Welfare Ind Arts and Culture
Languages:
English
Certifications:
License Instructor #171225 Madd Dog Athletics, License Instructor #171225
Temple University - QA/RA, West Chester University of Pennsylvania - Business Management
About:
Tara Dougherty is a Clinical Research and Regulatory Affairs professional with 5 years of experience in the Pharmaceutical and Biotechnology industries. Tara’s strengths include negotiation, problem ...
Tagline:
Clinical Regulatory Affairs Professional
Bragging Rights:
Received a Master of Science degree from Temple University School of Pharmacy in Quality Assurance and Regulatory Affairs