Himani L.
Junior Clinical Research Coordinator
Open to offersNew to PlatformAbout
Himani L. is a results-driven professional with a Bachelor of Pharmacy (Honors), poised to excel as a Clinical Research Coordinator. With significant experience in the pharmaceutical industry, her previous role as a Business Associate in Pharma honed her skills in GMP-compliant documentation and data entry and management, mirroring the standards required in clinical trial data management. Himani has hands-on training in pharmaceutical manufacturing and quality assurance, where she participated in GMP-compliant operations, lending direct expertise to clinical trial protocol and regulatory compliance. Her academic pursuits strengthened her understanding of clinical pharmacokinetics and drug regulatory affairs, while her research, including a presentation on meningitis treatment pathways, showcases her scientific communication prowess. Himani's proficiency in MS Excel supports her capability in maintaining meticulous records and supporting data-driven research operations.
Experience
Business Associate (Pharma)
null · 2025 — 2026Interpreted and conveyed technical pharmaceutical product data to healthcare professionals, acquiring skills relevant to clinical trial site coordination. Maintained detailed documentation of client interactions, sales records, and compliance data in MS Excel, adhering to clinical trial data entry standards. Conducted structured market surveys and competitor analyses, showcasing an analytical approach essential for clinical research. Addressed complex product queries from medical professionals, demonstrating clear communication of scientific information across diverse audiences.Intern – Pharmaceutical Manufacturing & QC
null · 2024 — PresentParticipated in manufacturing, packaging, and quality control operations while adhering to GMP-certified facility standards. Carried out in-process checks and monitored SOP adherence, which are directly applicable to clinical trial protocol compliance and safety monitoring. Recorded quality control observations and batch records, reinforcing the necessary rigorous record-keeping in clinical research. Developed a foundational understanding of pharmaceutical regulatory norms, preparing for ICH-GCP and clinical trial regulatory compliance.
Skills & Expertise
Education
- Bachelor of Pharmacy (Honors)SRIT Jabalpur · 2021 — 2025
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