Scientist

Emilio R. Almanzar

**** ****** *** **. ***#*** Tampa, FL 33619

Cell: 201-***-****

Fax: 201-***-****

***********@*****.***

OBJECTIVE:

Self-motivated professional seeking a challenging, rewarding position where I can utilize my communication skills, and research and development background.

Summary:

I have a vast experience in quality and compliance environment in the highly regulated healthcare industry. In addition, I have extensive experience with the following Quality Systems: Hedis Measures (MACRA & MIPS), Document and Records Management, Complaints Management, Change Control, Campaign Project Launch, and HIPPA Compliance Training. These broad range of exposures have allowed for me to develop strong documentation, analytical, and technical writing skills. Through my various experience, I have gained a thorough understanding of healthcare industry requirements and become proficient with quality assurance and auditing principles/procedures. I have also been involved in research & development of EHR, training physicians on platform and office SOPs. These experiences have brought additional development of my skills in high throughput data entry, transactional systems, and relationship building, where first-time-right quality is paramount for regulatory compliance.

EDUCATION:

Rutgers University, New Brunswick, New Jersey - Bachelor's Degree;

BS in Biotechnology/Biochemistry - May 2012

PROFESSIONAL EXPERIENCE:

02/2015 to PRESENT – Quality Standards SOP System Specialist / Business Development Team – Enable Healthcare Inc East Hanover, NJ

•Support and maintain GCP Systems

•Act as key member or leader of cross-functional teams on Business process, performance or System Enhancement Initiatives as required

•Provide technical advice/guidance, recommend possible resolutions and make decisions impacting scope of work, in conjunction with management where appropriate

•Arrange and provide training to SOP approvers (Line Function management) to ensure timely approval of process maps, thus complying with GCP regulations

•Manage first line support for physicians, legal, and staff users, proposing solutions to ensure minimal disruption to business activities. Managing end user questions/feedback providing resolutions as necessary. Regular liaison between IT Dept and software provider for GCP activities.

•Support and conduct GCP system audits.

•Create and update process maps (modeling) in collaboration with process expert(s), line function SMEs and QA training organization

•Responsible for organizing, conducting, and documenting GCP workshops and collegial review meetings with process experts and/or other SMEs

•Ensure continuous improvement of process modeling and tool methodology as well as develop/maintain GCP guidance documents for uniform quality throughout the SOP process maps and related documents

02/2016 to PRESENT –Project Manager – United Medical Billing, LLC Hackensack, NJ

•Project Management with a focus on Organization EHR

Training, Sales & Marketing, Presentation, Organized Documentation of SOAP notes.

•Designing and validating custom application, databases, and spreadsheets.

•Facilitate with Private Practices to discuss purpose, scope, and results of office billings and activities.

•Managed multiple business technology group clients and set expectations while consistently delivering results.

•Scope of Responsibility preparing SOPs: Credentialing, Medical Coding, Medical Billing, Internal Auditing, qualifying Patient for specific eligible services.

oFollow up on GCP SOP Deviations, audit reports, issue escalations

oInvestigate missing information and complete incomplete records

oClose out SOP Deviations, and audit reports

oReview investigation site and system audit reports.

oPerformed all activities in accordance with GCP.

•Daily contact with physicians, staff, and other parties.

•Developed and revised QA Audit SOPs, compliance tracking tools, and audit worksheets to improve processes and procedures

•Perform care gap analysis and risk assessment.

•Provided timely written reports of quality compliance status.

1/2012 to 5/2012 – Quality Assurances Quality Compliance – Aurobindo Pharmaceutical Dayton, NJ

•Conducted internal systems and process audits.

•Created internal process procedures and documents.

•Executed the preparation, distribution, tracking and filing of questionnaires to evaluate supplier quality systems for compliance.

Provided timely written reports of quality/regulatory compliance status.

•Compile reports of audit results to senior management.

•Collaborated with cross functional departments to assure seamless communication.

•Supported QA/GMP related Quality Systems in QA support functions to ensure GMP regulatory requirements, guidelines, and company standards.

•Updated the company standards and procedures and supported the implementation of the new procedures.

•Participated in local and global working groups as the QA representative.

•Project Management with a focus on Organization and GCP Training.

•Designing and validating custom application, databases, and spreadsheets.

•Facilitate with global management to discuss purpose, scope, and results of GCP audit findings and activities.

05/2010- 08/2010 – Research & Development – USDA Experimental Station TARS Mayaguez, PR

•Edited and formatted research publication on HSP70 gene editing as a research assistant.

•Studied multiple samples of soil from different parts of the country to determine optimal growth scenario.

•Prepared pest traps using different techniques including pheromones, to increase optimal growth conditions and reduce hazards.

•Studied terminalia flies: adjusted diet to determine protein uptake, behavior, and lifespan.

•Prepared grant proposals.

•Cloned multiple plants in the lab for future studies.

•Assembled literature and performed field activities according to SOPs.

Community Service:

2012 – United States Public Health Service: Volunteer for Hurricane Sandy Edison, NJ

•Assist USPHS in setting up shelter, dieticians and headquarters for Hurricane Sandy victims

2005 –2008 – Bergen Community College Paramus, NJ

•Head Tutor in Math and Science that was responsible for a staff of 7

•Head of the fitness center staff of 3

Skills

Technical: Proficient in Microsoft Office Products.

Lab: Blotting, PCR, Dilutions, Gel electrophoresis, HPCL, Cloning, Gene Editing, Cell culture

Language(s): Fluent in Spanish

REFERENCES AVAILABLE UPON REQUEST

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