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Candidate #348151

2-Week Notice

Brief Introduction

To work honestly, sincerely, and dedicated in any field related to my profession with a positive outlook in a life committed to the pursuit of excellence imbued with a deep sense of responsibility, integrity, and professionalism and also; to be able to learn new experiences and skills in the area that I work and so be a help to the institution that I work for; To be able to help and render my service to the people, especially to those who are in need in the blessing of our Almighty Father through the help of the institution.

Skillset

  • 7 years of relevant experience
  • Patient Charts
  • Serious Adverse Events
  • Databases
  • CAPA
  • English
  • Tagalog
  • Positive Attitude
  • Self-motivated
  • Sense of Responsibility
  • Standard Operating Procedure
  • Teamwork
  • Working Independently
  • ICP

Work Experience

  • Healthcare Virtual Assistant

    Aug 2022 - Jul 2024


    • Updates the patient chart records and insurance information. Responds to different inquiries about the clinic's healthcare services
    • Calendar management of doctors and patients. Insurance verification and prior authorization
    • Reason for Leaving: looking for a dayshift role

  • Pharmacovigilance Drug Safety Administrator

    Nov 2019 - Jun 2022


    • Coordinates the timely review of protocol inquiries, serious and non-serious adverse events, diagnostics and Data Safety Monitoring Board data; tracks all necessary data and generates reports for the client, project team and/or external vendors
    • Interfaces with various internal and external parties to implement projects, prepare Confidentiality Disclosure Agreements, Letters of Intent and Member Agreements based on contractual considerations; reviewing all contractual documents for accuracy and coordinating internal and external approvals
    • Compiles adjudication dossiers and creates/submits follow-up to investigative sites. Coordinates/facilitates project meetings, drafts meeting minutes, posts blinded and un-blinded minutes/materials to client portals and distributes to internal and external project teams
    • Manages project specific training and the set-up, maintenance and archival of program files; ensuring PVG remains audit ready
    • Identifies and redacts subject identifiers per local requirements, retrains sites and escalates re-occurrences to PPD Data Privacy
    • Performs data entry into internal/external databases, tracking systems and PPD's budget management system; performs system reconciliations to identify issues which may negatively impact project timelines
    • Answers incoming hotline calls, coordinates department functions and performs other duties as assigned. Supports any specific activities performed by the local office, which cannot be performed from elsewhere. Reason for Leaving: looking for a remote work set-up

  • Pharmacist in Charge (Quality Assurance Compliance)

    Apr 2017 - Nov 2019


    • Deviation Investigation Report / Atypical Investigation Program. Updates Deviation Investigation Report (DIR) Database. Conducts one on one monthly meeting and every other month group meeting. Monitors closure of CAPA and prepares monthly update and annual report
    • Artwork and Packaging Development. Proof read text details, checks accuracy and consistency of dimensional attributes and functionality of PM artwork
    • Coordinates with Material Control Team Leader on the item code of each PM. Coordinates with Regulatory Affairs Team Leader on the review of PM
    • Coordinates with printer and clients on artwork with comments/corrections, final approval and LSD approval
    • Monitors and document status of each PM on every step of the entire development process. Management of Packaging Component Specification (PCS). Initiation and revision of PCS. Identifies the companies and materials that require PCS. Prepares a PCS reference to client approved Packaging Material Inspection Report/Artwork as basis
    • Submit the accomplished PCS to QA team leader to check the completeness of information stated and to approve the PCS
    • Handled Packaging Material Complaints. Updates Packaging Material Complaint Spreadsheet. Control Issuance of the Packaging Material Complaint. Monitors closure of CAPA provided by the supplier of the Packaging Material and prepares quarterly and annual report. Reason for Leaving: proximity issues, had to relocate to home province

Education

  • Degree: Bachelor of Science

    Major: Duration: Jun 2012 - Apr 2016