Resumes
Resumes

Product Review Committee Planning Project Manager, Chief Scientific And Medical Officer
View pageLocation:
Chicago, IL
Industry:
Pharmaceuticals
Work:
Takeda Pharmaceuticals
Product Review Committee Planning Project Manager, Chief Scientific and Medical Officer
Takeda Pharmaceuticals Jun 2012 - Nov 2014
Project Manager, Therapeutic Area Global Project Manager
Abbott Apr 2011 - Dec 2011
Business System Analyst Consultant
Pfizer 2006 - 2010
Manager - Research Quality Assurance
Pfizer 2003 - 2006
Senior Specialist - Research Quality Assurance
Product Review Committee Planning Project Manager, Chief Scientific and Medical Officer
Takeda Pharmaceuticals Jun 2012 - Nov 2014
Project Manager, Therapeutic Area Global Project Manager
Abbott Apr 2011 - Dec 2011
Business System Analyst Consultant
Pfizer 2006 - 2010
Manager - Research Quality Assurance
Pfizer 2003 - 2006
Senior Specialist - Research Quality Assurance
Education:
The George Washington University 2011 - 2011
Illinois State University
Bachelors, Bachelor of Science Temple University
Illinois State University
Bachelors, Bachelor of Science Temple University
Skills:
Laboratory
Clinical Trials
Medical Writing
Planning
Ich Gcp
Cro
Organization and Prioritization Skills
Computer System Validation
Data Management
Gmp
Infectious Diseases
Gxp
Ctms
Biotechnology
Regulatory Affairs
Change Control
Validation
Quality Assurance
Regulatory Requirements
Building Effective Relationships
Pharmacovigilance
Drug Discovery
Quality System
Analytical Chemistry
Lifesciences
Protocol
V&V
Oncology
Gcp
Drug Development
Cross Functional Team Leadership
Clinical Development
Collaboration
Regulatory Submissions
Vaccines
Pharmacology
Strategic Thinking
Project Management
Pharmaceutical Industry
Proactive Self Starter
Technology Transfer
Glp
Lims
Toxicology
Capa
Fda
Sop
21 Cfr Part 11
Ind
Adaptability
Biopharmaceuticals
Clinical Trials
Medical Writing
Planning
Ich Gcp
Cro
Organization and Prioritization Skills
Computer System Validation
Data Management
Gmp
Infectious Diseases
Gxp
Ctms
Biotechnology
Regulatory Affairs
Change Control
Validation
Quality Assurance
Regulatory Requirements
Building Effective Relationships
Pharmacovigilance
Drug Discovery
Quality System
Analytical Chemistry
Lifesciences
Protocol
V&V
Oncology
Gcp
Drug Development
Cross Functional Team Leadership
Clinical Development
Collaboration
Regulatory Submissions
Vaccines
Pharmacology
Strategic Thinking
Project Management
Pharmaceutical Industry
Proactive Self Starter
Technology Transfer
Glp
Lims
Toxicology
Capa
Fda
Sop
21 Cfr Part 11
Ind
Adaptability
Biopharmaceuticals
