Technical Writer, Analyst
Federico “Fred” Marcano Jr.
Roselle, NJ
acuzpg@r.postjobfree.com / 908-***-****
Objective
Technical Writer/Analyst with over 14 years experience in the Pharma industry seeks a challenging opportunity within a dynamic application development environment.
Work Experience
Regulatory Affairs Operations Specialist
Target Health Inc. - NY
February 2016 to May 2016
Responsibilities
• Published regulatory documents (CSR, amendments, data lists, CRFs) for submission to FDA.
• Assembled file directories per client investigator/study administrator structure.
Technical Writer, Systems Analyst
Target Health Inc. – NY, NJ
April 2005 to January 2016
Responsibilities
• Supported Web clinical trials system with user/technical manuals, and online help guides.
• Ran test scripts to validate system functionality.
• Track application issues for remediation.
Technical Writer\Online Help Author
Innovative Technology Solutions - NJ
February 2005 to April 2005
Responsibilities
• Supported telecomm field report system with user manual, and test scripts.
• Integrated online help files to system screens.
• Wrote and tested installation and configuration guides for each system version.
• Issued problem tickets for remediation.
Sr. Technical Writer\Project Analyst
Schering-Plough (Global Animal Management Division) - NJ
April 2003 to February 2005
Responsibilities
• Supported animal health system with user/technical manuals, and test scripts.
• Integrated online help files to system screens, and managed tasks in project plan.
• Used Visual Source Safe to version control test scripts, documents and help files.
Sr. Technical Writer\Trainer
Bristol-Myers Squibb (Sargon Consulting) - NJ
June 2002 to March 2003
Responsibilities
• Supported a clinical trials lab system with user/technical documents, and test scripts.
• Integrated online help files to system screens.
• Submitted user documents and test scripts for version control.
• Tracked product issues for remediation.
Sr. Technical Writer\Trainer
Thor Technologies (obtained by Oracle) - NY
October 2000 to May 2002
Responsibilities
• Supported a security/identity access rights system with user/technical/training guides.
• Integrated online help files to system screens.
• Tracked product issues for remediation.
• Submitted user documents, help files, and test scripts for version control.
• Formatted documents per compliance with template standards and style guide.
Technical Writer
Starpoint Solutions – NY, NJ
October 1999 – September 2000
Responsibilities
• Wrote user guides/testing for client Portals (Lehman Live, CitiMarkets, PurePac Pharma)
• Submitted user, technical, and training documents for version control.
• Formatted documents per template standards and style guide.
Online Help Author/Technical Writer
NAVISYS - NJ
June 1997 – October 1999
Responsibilities
• Supported life insurance/annuity report system with user guides and technical manuals.
• Integrated online help files to system screens.
• Submitted documentation, online help files, and training materials for version control.
• Formatted documentation per template standards and style guide.
Education / Skills
A.A.S - Computer Science, CUNY Borough of Manhattan Community College – NY
Version Control, Document Management, SDLC, Analysis, Change Control, SOP, GCP/GMP, 21 CFR Part 11, Regulatory Affairs, Adobe Acrobat ISI Toolbox Pharma Ed., MS Office