SUMMARY:

• Detail oriented Project Manager with strong analytical abilities and an arsenal of transferable skills that establish a foundation of success in a variety of industries.
• Previous experience in with medical device development in an FDA regulated field, currently working within the P&C Insurance industry. Experienced in managing large IT projects (>100k hours) with multiple teams of onshore and offshore resources. Meticulously organized with a track record that shows tremendous growth in short periods of time.
• The combination of various skill sets shows not only my qualifications and strong foundation, but also my aptitude to excel.
• SDLC
• Portfolio Management at the Executive level
• Microsoft Suite (including Project and 365) JIRA, Planview and SharePoint
• Fluent in Agile and Waterfall methodologies
• Environment Coordination
• Fiscal budget forecasting
• Detail - oriented with strong follow through
• Exceptional communication and interpersonal skills
• Change Management
• Lead multi cross functional teams
• Vendor Management
• Data analysis
• Process optimization
• Resource management

PROFESSIONAL EXPERIENCE:

IT Project Manager

Confidential, Jacksonville, FL

Responsibilities:

• Responsible for the implementation and delivery of projects on time, within budget and with appropriate quality expectations
• Maintained and built out project schedule, worked with team leads to reserve resources and projected total effort needed to complete requirements
• Defined scope and objectives
• Experienced in Full SDLC
• Managed vendor contracts with budgets in excess of 60MM, coordinated onboarding and of offshore and onshore resources
• Provided immediate updates to SharePoint, Planview, and MS Project
• Implemented Change Control Review Committee to facilitate a proper channel for review, prioritization and management of change orders
• Manage, issues, and audit logs to prevent and mitigate risk
• Schedule environment deployments to align with business needs
• Assist in Development of Enterprise Portfolio Management, organizing a backlog of 150+ requests, prioritizing ranking of projects per team capacity and provided monthly Portfolio updates for Executive consumption

Project Analyst

Confidential, Jacksonville, FL

Responsibilities:

• Solely worked with Research and Development of Medical Devices
• Coordinated schedules and time lines between engineers and clinical trial staff
• Tracked development activities and managed multiple projects through data collection.
• Monitored time sensitive goals and objectives to exceed expectations
• Performs conceptual analysis and forecasting resource requirements
• Solving complex problems arising during ongoing projects
• Track plan cost versus actual cost to ensure budget adherence and the proper allocation of resources
• Conducts biweekly meetings to senior staff to share progress reports
• Utilized root cause analysis to define technical problems
• Worked closely with outside vendors to determine logistics, cost effective transactions, and contracts for use of proprietary information.
• Proficient in following established procedures, documentation collection, and making sure all products are in FDA clinical compliance.
• Defined and edited parameters needed for quality protocol development with principal investigators.
• Demonstrates understanding of quality systems
• Provided assistance in research and development, in the formulation of new therapeutic medical device technology, using problem-solving skills to deliver under huge restraints.

Quality Assurance Analyst/Chemist

Confidential, Jacksonville, FL

Responsibilities:

• Improved current systems and processes through identifying evolving technologies.
• Conducted logistics support plans life cycle management maintenance and other relevant operations.
• Provided recommendations for improvements in regular reports documents and technical briefings.
• Analyzed bulk chemical shipment samples, as well as in-process goods and finished products under GMP regulations.
• Assessed claim payment impacts and accuracy rates on a regular basis.
• Supervised dispersal of bulk product through manufacturing operations to ensure minimal microbiological contamination
• Worked with technicians in development of bulk batches
• Reviewed raw material selection
• Operated and maintained analytical instrumentation and prepared lab reports summarizing findings.
• Adhered to FDA mandates, cGMP guidelines and internal quality-control policies, proficient in aseptic laboratory techniques.
• Responsible for mentoring production staff in quality to help reduce micro contamination issues.

Insurance Verification Specialist

Confidential, Savannah, GA

Responsibilities:

• Coordinated patient data collation with various external referral sources.
• Initiated the pre-authorizations/pre-determinations for accurate insurance verification and processing to ensure patients receive treatment and medications within established patient/company standards.
• Maintained and revised procedural lists, control records and coded schemes to process source data
• Excellent familiarity with hospital and pharmacy environments
• Strong grasp of database integrity procedures
• Superior abilities with MS Office applications including Excel Access and Word
• Coordinated patient data collation with various external referral sources.
• Resolved disputes in collaboration with contract administrators.
• Maintained and conducted research in payer database.