beBee background
Pharmaceutical / Bio-tech
Ria De Sousa

Ria De Sousa

Clinical Trials
London, Greater London


About Ria De Sousa:

I am a highly motivated, adaptable, and detail-oriented individual with a robust background in clinical support roles and healthcare administration. I am looking for opportunities within clinical trials/ clinical research to advance my career. My inherent curiosity fuels my deep passion and unwavering commitment to advancing therapeutic approaches and enhancing patient outcomes for individuals grappling with various diseases. 


I have extensive experience in the NHS including roles as a healthcare assistant and vaccinator, where I excelled in patient care, vaccine administration, and adherence to safety protocols. Additionally, I served as a medical receptionist/administrator, managing patient check-ins and streamlining processes for improved patient satisfaction. In my role as a vaccine administrator, I significantly increased vaccine uptake among underserved populations. Moreover, my involvement as a student ambassador and returning officer demonstrates my commitment to community engagement, leadership, and mentorship, contributing to increased event attendance and successful committee appointments.


I hold a First-Class Hons BSc in Pharmacology and Innovative Therapeutics from a Russell Group university. My coursework encompassed essential topics like Drug Design, Translational Pharmacology, Clinical Trials, Regulatory Affairs, Cancer Biology, and Molecular Basis of Personalized Medicine. This education equipped me with a profound understanding of clinical research phases 1-5 and expertise in regulatory frameworks such as MHRA, EMA, and FDA. I also engaged in impactful research involving 3D bioprinting and the development of educational materials for primary school children. My commitment to ethical standards in clinical research is underscored by my completion of Good Clinical Practice (GCP) training. Furthermore, I prioritize patient perspectives and informed consent when interacting with clinical trial participants, enhancing their overall trial experiences.

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