Headline

Operations specialist 1 at IQVIA

About

With a PGDM in clinical research and a BPharm, I am a safety associate trainee at IQVIA, a global leader in providing innovative solutions for human health. In this role, I ensure the quality and compliance of pharmacovigilance (PV) activities and data, collaborating with internal and external stakeholders to monitor, report, and analyze adverse events and drug safety issues. I have over a year of experience in PV and data standardization, having also worked as a data standardization trainee at PointCross Life Sciences for three months. There, I supported the conversion and validation of clinical data sets using Six Sigma and Lean Six Sigma methodologies, improving the accuracy and efficiency of data processing. My core competencies include PV, data standardization, medical terminology, good clinical practice, and registered pharmacist. My mission is to contribute to the advancement of clinical research and patient safety by leveraging my skills and knowledge in the field. My values and goals are aligned with IQVIA's vision of improving human health outcomes and reducing healthcare burdens.

Location

Bengaluru

Work experience

Operations specialist 1 at IQVIA, Mar 2026 - Present · 4 mos

Drug Safety Associate at IQVIA, Apr 2024 - Mar 2026 · 2 yrs

Safety associate trainee at IQVIA, Apr 2023 - Mar 2024 · 1 yr

Data standardization trainee at PointCross Life Sciences, Nov 2022 - Jan 2023 · 3 mos, Bengaluru, Karnataka, India

Education

Master of Business Administration - MBA, Business analytics, Manipal Academy of Higher Education

Diploma of Education, Clinical research, Icbio institute of clinical research