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Tabina Ali Tramboo

M.Pharm candidate · Clinical Research & Pharmacovigilance

Srinagar, Jammu and Kashmir, India

@tabina_ali

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🎓 Master of Pharmacy at University of Kashmir · Graduated 2025

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About

Master’s in Pharmacy student at the University of Kashmir with hands-on experience in clinical research and industrial pharmaceutical training. Focused on clinical data, patient safety, drug safety monitoring, and research documentation, with interest in research management, pharmacovigilance, and regulatory affairs.

Experience

  • Clinical Research Intern
    SKIMS Hospital
    Apr 2024 – Nov 2025

    Assisted in coordination and technical execution of a clinical research project focused on pregnancy and cardiovascular disease; supported patient recruitment, informed consent, CRFs, data management, literature review, progress documentation, and interim reports.

  • Clinical Research Intern
    SKIMS Hospital
    Apr 2024 – Nov 2025

    Assisted in coordination and technical execution of a clinical research project focused on pregnancy and cardiovascular disease; supported patient recruitment, informed consent, CRFs, data management, literature review, progress documentation, and interim reports.

  • Clinical Research Intern
    SKIMS Hospital
    Apr 2024 – Nov 2025

    Assisted in coordination and technical execution of a clinical research project focused on pregnancy and cardiovascular disease; supported patient recruitment, informed consent, CRFs, data management, literature review, progress documentation, and interim reports.

  • Research Intern
    Sun Pharma
    Aug 2021 – Sep 2021

    Completed industrial training at a pharmaceutical manufacturing facility, observing and assisting in solid dosage formulation, packaging, process validation, documentation, equipment handling, batch manufacturing records, and quality control/testing workflows.

  • Research Intern
    Sun Pharma
    Aug 2021 – Sep 2021

    Completed industrial training at a pharmaceutical manufacturing facility, observing and assisting in solid dosage formulation, packaging, process validation, documentation, equipment handling, batch manufacturing records, and quality control/testing workflows.

  • Research Intern
    Sun Pharma
    Aug 2021 – Sep 2021

    Completed industrial training at a pharmaceutical manufacturing facility, observing and assisting in solid dosage formulation, packaging, process validation, documentation, equipment handling, batch manufacturing records, and quality control/testing workflows.

Education

Skills

1 to 2 years 1 to 2 years A year or two of steady use.
Research Patient Safety Medical Writing Literature Reviews Data Interpretation Good Clinical Practice Research ethics compliance
<3 months <3 months Just getting started - under three months. This is also what shows when a level has not been set.
Chemistry Pharmacology Pharmaceutics Pharmacokinetics Drug Formulation Pharmacovigilance Regulatory Affairs Drug safety monitoring Pharmaceutical Analysis Adverse Event Reporting Standard Operating Procedures Pharmaceutical Quality Assurance

Tools / apps / platforms

<3 months <3 months Just getting started - under three months. This is also what shows when a level has not been set.
Microsoft Word Microsoft Excel Microsoft Office Microsoft PowerPoint

Projects

  • Study of Anticoagulation Pattern (Novel Oral Anticoagulants/Vitamin K antagonists) of Patients Attending a Tertiary Care Centre

    Conducted an observational study evaluating usage patterns, efficacy, and safety of NOACs and VKAs in patients requiring long-term anticoagulation therapy; collected and analyzed patient data on dosage trends, INR monitoring, and clinical outcomes under supervision.

  • Study of Anticoagulation Pattern (Novel Oral Anticoagulants/Vitamin K antagonists) of Patients Attending a Tertiary Care Centre

    Conducted an observational study evaluating usage patterns, efficacy, and safety of NOACs and VKAs in patients requiring long-term anticoagulation therapy; collected and analyzed patient data on dosage trends, INR monitoring, and clinical outcomes under supervision.

  • Study of Anticoagulation Pattern (Novel Oral Anticoagulants/Vitamin K antagonists) of Patients Attending a Tertiary Care Centre

    Conducted an observational study evaluating usage patterns, efficacy, and safety of NOACs and VKAs in patients requiring long-term anticoagulation therapy; collected and analyzed patient data on dosage trends, INR monitoring, and clinical outcomes under supervision.

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