Kirandeep Jassi

Kirandeep Jassi

Trainee Scientific Officer

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location of Kirandeep JassiGreater Toronto Area, Canada

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  • Timeline

  • About me

    Actively seeking career opportunities in Pharmacovigilance/ Drug Safety/ Pharmacovigilance Associate/ Analyst/ Medical Writing/ Clinical Research

  • Education

    • Lawerance Public Sen Sec Public, Mohali

      2002 - 2007
    • CRA School of Montreal, Canada

      -
      Clinical Research Coordinator
    • Panjab University,Chandigarh

      2010 - 2012
      Master of Science - MS Microbial Biotechnology
    • Fleming College

      2022 - 2022
      Postgraduate Degree Project Management
  • Experience

    • Orbit Biotech

      Aug 2014 - Aug 2016
      Trainee Scientific Officer

      • Taught Industrial Training courses for Microbiology, Molecular Biology and Fermentation.• Trained International Research Project Interns from Belgium, Probiotic Research Project Interns from various streams including Bachelors' and Masters' students.• Worked on editing BioSmart Publication products (Ace The Race, Ace The Race Plus, Sprint and Quants Masters) and other educational online service.

    • PAREXEL

      Feb 2017 - Feb 2022

      • Managed Individual Case Safety Reports (ICSRs) across various case types, including triaging for expedited reporting and ensuring timely submissions to regulatory authorities.• Registered and initiated ICSRs into the safety database, conducting duplicate searches and managing duplicate cases appropriately.• Coded ICSRs, determined expectedness of adverse events, wrote case summaries, assessed causalities, and provided company comments as needed.• Conducted data validation by cross-checking against source documentation.• Interacted with clients regarding pharmacovigilance activities and communicated with patients and healthcare professionals about adverse drug reactions (ADRs).• Developed narrative templates for Individual Clinical Study Reports (ICSRs), assessing clinical and safety database outputs for relevant information while ensuring complete and high-quality data entry into database like ARGUS, SCEPTRE, PRIMO.• Performed quality checks of ICSRs and Serious Adverse Event (SAE) narratives, ensuring compliance with client SOPs and regulatory requirements. • Report Adverse Events/Severe Adverse Events (AE/SAEs) following approved SOP’s.• Coded over 3,000 cases and maintained up-to-date knowledge of pharmacovigilance guidelines from Health Canada, US FDA, EMEA, and ICH. عرض أقل

      • Pharmacovigilance Analyst

        Feb 2017 - Feb 2022
      • Pharmacovigilance Scientist

        Feb 2017 - Oct 2018
    • Dollarama L.P.

      May 2022 - Sept 2022
      Cashier Customer Service
    • Safety Plus, Inc.

      Oct 2022 - now
      Administrative Assistant

      • Preparing, typing, and editing correspondence and invoices.• Receiving and distributing incoming mail efficiently.• Ordering office supplies and maintaining inventory levels.• Scheduling and confirming appointments and meetings.• Participating in the hiring and training process for new truck drivers.• Preparing paperwork for company audits.• Coordinating the flow of information internally and with other departments, monitoring and reviewing Hours of Service (HOS), and detecting violations in Electronic Logging Devices (ELD) and paper logs, taking appropriate corrective actions.• Handle incoming and outgoing mail.• Applying for Fast Cards for USA travel. عرض أقل

  • Licenses & Certifications