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SL

Sindhura Lankireddy

Pharmacovigilance Associate · M.Pharm Graduate

Hyderabad, Telangana, India

@sindhura1

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About

M.Pharm graduate with an Advanced PG Diploma in Clinical Research, Pharmacovigilance and Clinical Data Management, and 1 year of experience in a GMP-regulated pharmaceutical quality control lab. Trained in ICSR data entry and quality review, MedDRA coding, query follow-up, narrative writing, literature screening, and exposure to Argus Safety.

Experience

  • QC Analyst
    Smilax Laboratories Limited · Hyderabad
    Feb 2014 – Mar 2015

    Tested quality of tablets, capsules and pellets as per approved SOPs. Reviewed test data against approved SOPs and specifications for completeness, accuracy and compliance. Recorded observations, calculations and results accurately under Good Documentation Practices, prepared and submitted batch testing records on time, supported audits, and worked in a GMP-regulated environment.

Education

  • Master of Pharmacy (M.Pharm)
    SIMS College of Pharmacy
    Awarded by Acharya Nagarjuna University
    Pharmaceutical Analysis · 2011 – 2013
  • Bachelor of Pharmacy (B.Pharm)
    St. Ann's College of Pharmacy
    Awarded by JNTU Kakinada
    2007 – 2011
  • Intermediate
    Vikas Mahila Residential Junior College
    2005 – 2007
  • SSC
    Arunodaya High School
    2004 – 2005
  • Advanced PG Diploma in Clinical Research, Pharmacovigilance & Clinical Data Management
    Cliniminds

Skills

1 to 2 years 1 to 2 years A year or two of steady use.
Audit Support Quality control
<3 months <3 months Just getting started - under three months. This is also what shows when a level has not been set.
Data entry Data Review Meddra Coding Quality Review Query Management Signal Detection Regulatory Compliance Good Documentation Practices

Languages

Fluent Fluent Comfortable using it for work.
Telugu Speak English Speak
Basic Basic A few words and simple phrases.
Hindi Speak Kannada Speak

Projects

  • Clinical Research Project: CTRI Study and Clinical Trial Site Visits
    CTRI

    Reviewed registered trials on CTRI and visited trial sites to observe informed consent, documentation and protocol-related workflows.

  • Pharmacovigilance Project: Literature Surveillance of Semaglutide
    PubMed

    Searched publications for patient, reporter, medical history and adverse event details, performed preliminary ICSR validity assessment, and flagged publications needing further evaluation.

Courses & certifications

  • Advanced PG Diploma in Pharmacovigilance · Cliniminds · 2026

🎯 Hobbies & interests

  • Listening Music
  • Gym
  • Drawing
  • Exploring Places

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