Amruta A. Dadmal – The Rising Star of Clinical Research You Need to Know About!

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AMRUTA A. DADMAL
Address: Plot no.45, Dhanwantari Nagar, Umrer Road, Nagpur 440024

SUMMARY
Detail-oriented Clinical Research professional with 1 year of hands-on experience supporting clinical trials in hospital settings. Skilled in patient interaction, data documentation, GCP compliance, and working with interdisciplinary teams. Passionate about contributing to evidence-based medical research to improve patient outcomes.

EDUCATION

  • MSc in Clinical Research
    School of Allied Health Sciences, Datta Meghe Institute of Medical Sciences (Deemed University)
    2024 | 72%
  • PG Diploma in Clinical Research, Pharmacovigilance, and Medical Coding
    Spruce Institute
    2021 | Grade: A
  • BSc in Biotechnology and Microbiology
    Shri Shivaji Science College, RTM Nagpur University
    2020 | 67%
  • Higher Secondary Certificate (Science)
    Vishwas Junior College, Maharashtra State Board
    2016 | 67%

CERTIFICATIONS

  • Good Clinical Practice Certification
  • Students of congress on application of emerging technologies (SCAET)2020 participation Certificate

SKILLS

  • Clinical Skills: Informed Consent, Patient Interaction, Adverse Event Reporting, Clinical Trial Monitoring
  • Technical Skills: Electronic Data Management, MS Office, Medical Writing
  • Regulatory Knowledge: Good Clinical Practices (GCP), ICH Guidelines, Pharmacovigilance
  • Soft Skills: Communication, Ethical Awareness, Team Collaboration

EDUCATIONAL WORKING EXPERIENCE

  • Clinical Research Intern*
    NKP Salve Institute of Medical Sciences and Lata Mangeshkar Hospital, Nagpur
    Mar 2024 – Feb 2025
    Assisted in execution of clinical trials across departments including ENT, Orthopedics, Surgery, and Cardiology.

EXPERIENCE

  • Conducted informed consent procedures for over 50 patients, ensuring ethical and legal compliance.
  • Collaborated with principal investigators and patients to ensure protocol adherence.
  • Maintained electronic data capture and clinical trial documentation.
  • Observed and recorded adverse events under supervision.
  • Contributed to projects involving osteoarthritis, diabetic foot ulcers, pressure ulcers, and cardiovascular diseases.

PUBLICATIONS

  • Estimation of prevalence of risk factor of hypertension among the population of Wardha district between the age group of 35-60 years: a study protocol
  • Nature’s Gold (Moringa Oleifera): Miracle Properties
  • Critical Appraisal of Drug Promotional Literature in Accordance With WHO Guidelines
  • Symphony of Science: Harmonizing Randomization Procedures Across Clinical Trial Phases

DECLARATION
I hereby declare that the above information given by me is true to the best of my knowledge and belief.
Date: 08/May/2025
NAME: Amruta Arvind Dadmal MSc Clinical Research
Place: Nagpur

Keywords: Clinical Research, Patient Interaction, GCP Compliance, Data Documentation, Informed Consent, Adverse Event Reporting, Electronic Data Management, Good Clinical Practices, Pharmacovigilance, MS Office, Medical Writing, Communication, Team Collaboration.

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