
Jeannerey Arien Macabebe
Community Pharmacy Intern

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About me
Application Manager at NNIT
Education

University of the Philippines- Manila
2008 - 2014Bachelor of Science (BS) Industrial PharmacyActivities and Societies: Alpha Phi Omega Sorority (UP Manila Chapter), University of the Philippines- College of Pharmacy Student Service League, Agapay, Kalinga at Kwentong Alay ng mga Pharmaceutico (AKKAP)
Experience

Mercury Drugstore
Apr 2011 - May 2011Community Pharmacy Intern
Univesrity of the Philippines- Philippine General Hospital
Apr 2013 - May 2013Hospital Pharmacy Intern
La Croesus Pharma, Inc.
May 2013 - Jun 2013Industrial Pharmacy Intern
University of the Philippines- Philippine General Hospital
Oct 2013 - Nov 2013Clinical Pharmacy Intern
Generika drugstore
Feb 2014 - Apr 2014Community Pharmacy intern
Food and Drug Administration Philippines
Aug 2014 - Apr 2016Verified the registration status, labeling compliance and authenticity of sample submittedEvaluated donated imported drug products with subsequent issuance of Certificate of Product Registration for DonationPerformed drug-related researchesResource Speaker for QPIRA Training Seminar Workshop and Licensing Seminar Product Verification Officer: verified the registration status, labeling compliance and authenticity of sample submittedPerformed drug-related researchesResource Speaker for QPIRA Training Seminar Workshop and Licensing Seminar Product Verification Officer: verified the registration status, labeling compliance and authenticity of sample submittedPerformed drug-related researches
Food Drug Regulation Officer II
Jan 2016 - Apr 2016Pharmacist II
Jan 2015 - Dec 2015Pharmacist I
Aug 2014 - Dec 2014

PPD
Apr 2016 - Jul 2021• Acts as liaison between the management and the team and serves as the contact person for team and workflow issues.• Assists management in client meetings and audits (internal and client), such as preparation of presentation slides and minutes of meeting among others.• Attends client meetings.• Conducts team meetings with the local team.• Assists with writing, reviewing and revising of Standard Operating Procedures (SOPs) and guidance documents in response to client directives or regulatory requirements.• Oversees day to day team activities (workflow, team allocation and client deliverables).• Assists management with day-to-day management operational needs. • Ensures compliance to client and regulatory requirements and escalates issues to the management.• Serves as mentor to the team for all workflows.• Assigns and conducts training to team members.• Assists in preparation and review of regulatory reports.• Coordinates with other departments regarding local regulatory submissions.• Performs quality review of adverse event reports and local submission documents.• Generates reports from database as per guidance and as required by the client.• Performs case receipt, case logging, triage, case processing, quality review and submission of adverse events from post market and clinical trial reports. • Performs reconciliation of databases and trackers. Show less • Acts as liaison between the management and the team and serves as the contact person for team and workflow issues.• Assists management in client meetings and audits (internal and client), such as preparation of presentation slides and minutes of meeting among others.• Attends client meetings.• Conducts team meetings with the local team.• Assists with writing, reviewing and revising of Standard Operating Procedures (SOPs) and guidance documents in response to client directives or regulatory requirements.• Oversees day to day team activities (workflow, team allocation and client deliverables).• Assists management with day-to-day management operational needs. • Ensures compliance to client and regulatory requirements and escalates issues to the management.• Serves as mentor to the team for all workflows.• Assigns and conducts training to team members.• Assists in preparation and review of regulatory reports.• Coordinates with other departments regarding local regulatory submissions.• Performs quality review of adverse event reports and local submission documents.• Generates reports from database as per guidance and as required by the client.• Performs case receipt, case logging, triage, case processing, quality review and submission of adverse events from post market and clinical trial reports. • Performs reconciliation of databases and trackers. Show less
Senior Safety Specialist (Team Lead)
Apr 2021 - Jul 2021Safety Specialist (Team Lead)
Sept 2019 - Mar 2021Safety Specialist
Apr 2018 - Aug 2019Associate Safety Specialist
Apr 2016 - Mar 2018

IQVIA
Jul 2021 - May 2024Assoc ManagerManage Safety Staff responsible in delivering services in Safety Operations under the guidance of senior management. May contribute to Global initiatives. Work in close collaboration with Senior Management and other relevant stakeholders supporting the achievement of local and global deliverables and metrics.

NNIT
May 2024 - nowApplication Manager
Licenses & Certifications

Pharmacist Licensure Examination
Professional Regulation CommissionJun 2014
ITIL Foundation Certificate in IT Service Management
PeopleCertJul 2025
Languages
- enEnglish
- fiFilipino
- spSpanish
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