Joy M.

Joy M.

Clinical Research Associate I

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  • Timeline

  • About me

    Senior Trial Manager, Evidence Solutions at AbbVie

  • Education

    • University of the Philippines

      1996 - 2002
      Bachelor of Science Industrial Pharmacy
  • Experience

    • Astellas Pharma

      Jan 2005 - Dec 2005
      Clinical Research Associate I

      Conducted investigator and site selection, site initiation, monitoring, data cleaning and study close-outin 5 sites for one study on bone metastases among cancer patientsLICENSE & CERTIFICATIONSForeign Pharmacy Graduate Equivalency Certificate, Foreign Pharmacy Graduate EquivalencyCommittee, United States of America, September 2008Pharmacy License, Professional Regulation Commission, Manila, Philippines,; Training while employed at PAREXEL and PPD is available upon request.Global Monitoring and Study Management Workshop, includes group discussions on actualmonitoring issuesBayer Schering Pharma Asia-Pacific Clinical Operations, Sept 16-20, 2008Global Monitor's Conference, includes discussions on study monitoring cases and issuesBayer Schering Pharma Global Clinical Operations Show less

    • Bayer

      Jun 2007 - Nov 2008
      Clinical Research Associate I

      Conducted investigator and site selection, site initiation, and monitoring for a study on an antibiotic foracute exacerbation of chronic bronchitisConducted monitoring, site close-out, and data cleaning for a study on hormone replacement therapyJoy Maglambayan, B.Sc Page 2 of 3Revised: 01 Feb 2013Managed the conduct of 5 post-marketing surveillance studies on antibiotics, oncology, anddiagnostics imaging, which includes planning, implementation, and data cleaning of the studies, aswell as training of medical sales representatives Show less

    • PPD

      Nov 2008 - Dec 2011

      Identified potential investigators in collaboration with the client company to ensure the acceptability ofqualified investigative sitesPerformed and coordinated assigned aspects of the clinical monitoring process in accordance withGCPs and global SOPs to assess the efficacy and safety of investigational products and/or medicaldevicesConducted site pre-study visits to ensure a site has adequate resources to conduct a studyConducted site initiation visits to ensure the site personnel are well-trained and well-informed prior topatient enrollmentPerformed periodic site monitoring visits to ensure a site is conducting a trial according to theprinciples of ICH-GCP, the study protocol, and all applicable rules and regulationsDeveloped collaborative relationships with investigative sites and client Show less

      • Senior Clinical Research Associate

        Mar 2011 - Dec 2011
      • Clinical Research Associate Level II

        Nov 2008 - Mar 2011
    • GlaxoSmithKline, insourced from Parexel

      Dec 2011 - Aug 2013
      Regional Study Manager

      Responsible for the development and implementation of regional clinical operations strategyEnsures consistency of and adherence to global clinical standards worldwideEnsures that clinical research is cost effective by analyzing internal and external costs, resourceutilization and performance dataPlan and identify resources for regional clinical studies based on project timelinesNegotiate and establish contracts with external resourcesIdentify emerging trends/regulations in clinical research while proactively integrating these elementsinto policies and proceduresDevelopment of training programs for internal and external resourcesAssist and participate in other Clinical Affairs projects or clinical studies as required Show less

    • PRA Health Sciences

      Aug 2013 - Jan 2016
      Clinical Team Manager II

      Managed clinical operations teams for Phase 3 clinical trials under different therapeutic areas

    • Allergan

      Feb 2016 - May 2020
      Senior Study Manager
    • AbbVie

      May 2020 - now
      Senior Trial Manager, Evidence Solutions
  • Licenses & Certifications