sameera shabnam
Clinical Process Associate - Document Specialist (eTMF) · IQVIA
About
PharmD graduate with experience in clinical research and eTMF documentation. I have 8 months of experience as a Clinical Process Associate at IQVIA, with exposure to Veeva Vault, document management, quality control, and ICH-GCP compliance. I’m looking to build a long-term career in clinical research, clinical data management, pharmacovigilance, or related healthcare research roles.
Looking for
I’m looking for opportunities in clinical research, clinical data management, eTMF/document management, pharmacovigilance, medical writing, or regulatory affairs. I’m particularly interested in roles where I can use my PharmD background and clinical research experience, learn from experienced teams, and grow into a long-term career in the life sciences industry.
Skills
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