Hello, and welcome to my professional profile!
I am a seasoned scientist with experience in the pharmaceutical/clinical research sector. Upon completion of my undergraduate degree, I spent a few years working as Quality Assurance Analyst in Pharmaceutical Medicine before moving to UK to obtain a master’s degree from Nottingham Trent University. Currently, I’ve achieved both BSc (4.2/5.0 CGPA) and MSc (Distinction/High Commendation) in Pharmacology. My extensive background in pharmacology, combined with my passion to improve health outcomes through Research & Development, has provided me with the tools necessary to progressively grow in this exciting industry.
As a Medical Scientist for Pharmora and contracted to a large global pharmaceutical company, I have worked within several therapeutic areas (Oncology, Vaccine and Immune therapies) and provided clinical support in multiple Phase II-III clinical trials ensuring the clinical data reporting was accurate and in compliance with regulations. Examples of some of my responsibilities includes Development & Review of key-study related documents for governance bodies such as DRC/PRC, IEC/REC and regulatory submissions (BLA/NDA), clinical data review, providing scientific input into design, implementation and execution of clinical trials etc.
Through Pharmora, I have gained valuable experience and a deep understanding of clinical development processes, medical terminologies, use of clinical databases, data collection and analysis, medical coding, adherence to regulatory guidelines and so on. I possess a proven-track record of delivering high-quality outputs and a demonstrable dedication of excellence to every project I work on, which contributed significantly in being recognized for top performance and receiving a fast-track promotion within 12 months in my role.
In my spare time I enjoy cooking, travelling, meditating and talking to friends/family.