Hudha Nasrin
Aspiring clinical research professional/Pharm D/Advanced diploma in clinical research holder/expertise in clinical trial terminologies and documentation
- Role
- Clinical Research Intern at Agile Cas
- Location
- Bengaluru, IN
- LinkedIn followers
- 500 followers
About Hudha Nasrin
I am a passionate and results-driven PharmD graduate with 1.5 years of experience as a…
Experience
Clinical Research Intern
Feb 2025 — Present · Bengaluru, IN
Throughout this program, I have developed a keen eye for detail, strong analytical skills, and a commitment to upholding the highest standards of patient safety and data quality. I am enthusiastic about applying these skills in a professional setting and contributing to the advancement of healthcare through clinical research.Clinical Research (CR): Understanding of clinical trial phases, Good Clinical Practice (GCP) guidelines, and ethical considerations in human subject research.Clinical Data Management (CDM): Proficiency in Case Report Form (CRF) design, data validation, and ensuring data integrity throughout the clinical trial process.Pharmacovigilance (PV): Skills in adverse event reporting, signal detection, and risk-benefit analysis to ensure drug safety and efficacy.Regulatory Affairs (RA): Knowledge of global regulatory requirements, submission processes, and compliance standards for drug approval and market authorization.Medical Writing: Ability to craft clear, concise, and regulatory-compliant documents, including clinical study reports, informed consent forms, and investigator brochures.
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