Clinical trial assistant
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I am a dedicated and detail-oriented PharmD graduate with an International Master’s in Global Health Management and over three years of hands-on experience in clinical research, particularly in oncology and gastroenterology studies. My professional journey has included roles as a Clinical Research Associate and Coordinator, where I gained substantial experience in managing clinical trials from initiation to close-out, ensuring adherence to ICH-GCP guidelines, regulatory compliance, and effective stakeholder communication. I bring strong skills in data management, protocol compliance, and administrative support, coupled with a proactive approach to problem-solving and collaboration.
With a proven ability to work efficiently within multidisciplinary teams and a passion for delivering high-quality research outcomes, I am eager to contribute to advancing clinical trials within the UK’s healthcare and research environment.
I have over three years of professional experience in clinical research, having worked as a Clinical Research Associate and Coordinator in India. During this time, I was involved in all phases of clinical trials, particularly in oncology and gastroenterology. My responsibilities included trial setup, patient recruitment, data management, regulatory compliance, and communication with sponsors and CROs.
I have supported both investigator-led and industry-sponsored studies, ensuring adherence to ICH-GCP guidelines and contributing to high-quality trial outcomes through strong administrative and operational support.
I hold a Doctor of Pharmacy (PharmD) degree and an International Master’s in Global Health Management. This academic foundation has equipped me with strong clinical knowledge, research methodology expertise, and a global perspective on healthcare systems and public health challenges, which I apply effectively in clinical research settings.