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Project Analyst And Co - Ordinator Resume

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SUMMARY:

Pharma & IT professional with organizational skills. Strengths include business analysis, technical writing, documentation, QA, testing, web development and project management. Projects include pharmaceutical, clinical research, quality, outsourcing, validation, data warehouse, transition, B2B eCommerce and electronic banking transactions. Web & social media projects, managing my own small home business, micro business analysis, technical writing, blogging, business development and record keeping.

PROFESSIONAL EXPERIENCE:

Project Analyst and co - ordinator

Confidential

Responsibilities:

  • Set up and ran a local community non profit that benefits the community. It is a recycling group similar to freecycle.
  • My group has over a thousand members.
  • I administer all moderator and owner functions for the group.
  • Web & social media projects, managing small business, micro business analysis, technical writing, business development.

Business Analyst

Confidential

Responsibilities:

  • Validation Documentation Specialist/ Analyst, GIT SPRI, GLP Documentation of User and Functional requirements for Calibration update system using LIMS Labware.
  • Analyst/Technical Writer, Analytical Development SPRI, GLP Documented SAS applications, SQL macros and wrote test scripts for the Stability area.
  • Company procedures, templates, regulatory requirements, compliance, quality assurance and processes & project methodologies were followed.
  • Owned the completion of documentation below, talked to management, staff & others as necessary
  • Write System Design Specifications & user manuals IQ/OQ/PQ/UAT & testing related documentation Assist with the execution of testing efforts
  • Assist with additional project or team documentation

Technical Writer

Confidential

Responsibilities:

  • Business Analyst, Documentation of user and functional requirements for computer system.
  • Technical Writing, system analysis, documented applications, wrote macros and tested functionality.
  • Procedures, templates, requirements, quality assurance and methodologies were followed.
  • Talked to management, staff & others as necessary
  • Write design specifications & user manuals & test documentation.
  • Assist with additional project or team documentation

Documentation writer

Confidential

Responsibilities:

  • Clinical Research Documentation Analyst & Tester Manage the testing effort for the secure file transfer project of the Clinical Electronic Business unit.
  • Produce and execute detailed SOP compliant CFR part 11 System Integration
  • Testing test scripts based on analysis of business, functional and system specifications to test various client-server and web-based applications.
  • Manage the SIT testing effort, including answering tester questions, reporting and tracking system errors and their resolution, providing status to management.

Technical Writer

Confidential

Responsibilities:

  • Validation Documentation Project Technical Writer GCP
  • Remediation of all clinical trial system applications to meet quality & validation audits.
  • Create functional requirements specifications and traceability matrix in Documentum to pass regulations.
  • Work with Office Templates and create macros.
  • Evaluate current documentation standards Create project plans to manage schedule
  • Create additional diagrams to document the system

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