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Lynda De VriesLD

Lynda De Vries

Medical information specialist/PV associate

€ 390/dag
Amsterdam, NL
8-15 jaar

Gemiddelde responstijd: 1 uur

Over Lynda

Experienced in providing medical information and contributing to pharmacovigilance in the pharmacy and pharmaceutical industry as pharmacist.

I am determined, adaptable, persistent and a great asset to the team.

Current project is accompanying the externalisation of OTC drugs.

I speak and write well Dutch, French, and English. I started career in the medical and medical device sector in which I obtained an experience of 7 years in the community pharmacy, 3 years in the clinical pharmacy, 1 year in the hospitalization at home sector and the E-health sector. Since 2020 I works in the Pharmacovigilance/medical/quality information sector.
  • Engels

    Tweetalig / moedertaal

  • Nederlands

    Tweetalig / moedertaal

  • Frans

    Tweetalig / moedertaal

  • Italiaans

    Basiskennis

Kan op locatie werken
Amsterdam (tot 50km)

Werkervaring

  • JOB SANOFI-OPELLA
    MEDICAL INFORMATION SPECIALIST TIER 2 BE/LUX/UK/NI
    oktober 2023 - Vandaag (2 jaren en 8 maanden)
    • Providing medical information using client approved resources (IRMS, Salesforce) in Dutch, English and French
    • Reporting and detecting adverse events and/or product complaints
    • Managing the client’s email inbox and incoming phone calls
    • Handling escalated inquiries on tier 1 and tier 2 level
    • Providing regular support/feedback/training to MICC external supplier
    • Performing quality control of MICC external supplier
    • Developing and maintaining scientific response documents
    • Creating/updating SOPs, Job aids for local Medical Information procedure
    • Participating at meetings with other departments such as Medical Affairs, Quality, Pharmacovigilance, and Regulatory
    • Identifying and forwarding AEs/PTCs to PV/QA department
    • Handling customer service complaints
    • Handling RA product updates
    • Performing test calls
    • Performing reconciliations with communications, PV and QA
    • Participating to monthly Business Review meeting
    • Participating to 6 monthly cross functional meetings with all departments
    • Creating training slides for MICC and sales representatives


  • Cognizant
    PHARMACOVIGILANCE ASSOCIATE
    oktober 2020 - oktober 2023 (3 jaren)
    • Case entree, translating of AE reports from DU/ FR to EN,
    • Safety narrative writing
    • Making FU query letters,
    • Quality check of case entree
    • Translation
    • Literature screening
    • Leading calibration calls
  • PPD
    MEDICAL INFORMATION SPECIALIST TIER
    maart 2020 - oktober 2020 (7 maanden)
    Cambridge, UK
    • Providing medical information using client approved resources (IRMS, Salesforce), reporting
    • Detecting adverse events and/or product complaints
    • Managing the client’s email inbox and incoming phone calls

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Opleidingen

  • MSC
    UNIVERSITY UTRECHT
    2012
    MSC
  • PHARMACOVIGILANCE REGULATORY PROCESSES
    2017
    PHARMACOVIGILANCE REGULATORY PROCESSES

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