Jasna Simičić

Medical Affairs Manager at PREMIUM Pharma Serbia
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Contact Information
us****@****om
(386) 825-5501
Location
Serbia, RS
Languages
  • English Professional working proficiency
  • Serbian Native or bilingual proficiency
  • Croatian Native or bilingual proficiency
  • German Elementary proficiency

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Credentials

  • Critical Thinking for Better Judgment and Decision-Making
    LinkedIn
    Sep, 2020
    - Oct, 2024
  • Developing Your Emotional Intelligence
    LinkedIn
    Sep, 2020
    - Oct, 2024
  • Embracing Unexpected Change
    LinkedIn
    Sep, 2020
    - Oct, 2024
  • Managing Stress for Positive Change
    LinkedIn
    Sep, 2020
    - Oct, 2024
  • Marketing on LinkedIn
    LinkedIn
    Sep, 2020
    - Oct, 2024
  • Strategic Thinking
    LinkedIn
    Sep, 2020
    - Oct, 2024
  • The Six Morning Habits of High Performers
    LinkedIn
    Sep, 2020
    - Oct, 2024

Experience

    • Serbia
    • Pharmaceutical Manufacturing
    • 1 - 100 Employee
    • Medical Affairs Manager
      • Sep 2020 - Present

      • R&D - Product development • Regulatory affairs - Product registration • Creating scientific and medical communication messages • Content and scientific writing (website, blogs, social media) • Manage brand-related medical information • Provide oversight for promotional activities • Create, review, and approve medical marketing materials. • Develop and present medical training to internal and external stakeholders. • Establishing credibility with KOLs • R&D - Product development • Regulatory affairs - Product registration • Creating scientific and medical communication messages • Content and scientific writing (website, blogs, social media) • Manage brand-related medical information • Provide oversight for promotional activities • Create, review, and approve medical marketing materials. • Develop and present medical training to internal and external stakeholders. • Establishing credibility with KOLs

    • Pharmaceutical Manufacturing
    • 1 - 100 Employee
    • Scientific Officer, Medical Science Liaison
      • Feb 2018 - Aug 2020

      • Scientific and dietary supplement expert • Regulatory affairs – represent the company in discussions with regulatory agencies about clinical matters relating to existing and future products, preparing and submitting all regulatory documents. • Content and medical writing (blogs, brochures, presentations, abstracts and scientific papers) • Responding to health care professional’s inquiries about products • Support corporate teams on scientific-related topics • Attending and speaking at medical conferences • Organizing scientific meetings • Establishing and maintaining peer-peer relationships with leading Research Institutes, Universities, MDs and Principal Investigators • R&D project management (involved in the design of preclinical and clinical studies, scientific experiments, development of the new products) • Writing and submitting patent applications • Project budgeting • Closely cooperating with marketing department ensuring understanding of the complex scientific findings, piloting innovative ways of delivering training to field-based physicians, scientist and medical personnel • Organize and analyze data, interprets and writes clinical and non- clinical reports to derive key outcomes and messages. Translate complex scientific issues for diverse audiences • Correspondence with international partners and distributors • Market analysis • Staying up to date with current relevant scientific publications Show less

    • India
    • Appliances, Electrical, and Electronics Manufacturing
    • Licensed Pharmacist, Pharmacy Manager
      • Sep 2010 - Feb 2018

      Head of the pharmacy team. Responsible for overseeing everyday operations of a pharmacy. Preparing medicines, recruiting and training staff, maintaining stocks, liaising with suppliers, implementing sanitary-control regulations, updating pharmacological knowledge and solving patient inquiries. Comply with entire laws governing pharmacy practice and drugs distribution. Head of the pharmacy team. Responsible for overseeing everyday operations of a pharmacy. Preparing medicines, recruiting and training staff, maintaining stocks, liaising with suppliers, implementing sanitary-control regulations, updating pharmacological knowledge and solving patient inquiries. Comply with entire laws governing pharmacy practice and drugs distribution.

    • Switzerland
    • Biotechnology Research
    • 100 - 200 Employee
    • Regulatory Affairs Assistant
      • Aug 2008 - Jul 2009

      Preparing, reviewing and submitting regulatory submissions to the regulatory authorities within company timelines and in accordance with regulatory guidelines and applicable national and international laws. Coordinating and completing reports required by regulatory authorities, maintaining complex files and electronic document management systems, and working with project teams to accomplish company goals. Preparing, reviewing and submitting regulatory submissions to the regulatory authorities within company timelines and in accordance with regulatory guidelines and applicable national and international laws. Coordinating and completing reports required by regulatory authorities, maintaining complex files and electronic document management systems, and working with project teams to accomplish company goals.

Education

  • Medical Faculty, Department of Pharmacy, University of Novi Sad,Serbia
    MSc, Pharmacy
    2003 - 2009
  • Gimnasium "Dušan Vasiljev", Kikinda
    1999 - 2003

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