Clinical Trial Assistant
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Managed trial documentation and research databases, ensuring 100% compliance with GCP and university protocols.
Supported data collection and participant monitoring, reducing errors in case report forms (CRFs).
Assisted in training new staff members, improving onboarding efficiency and compliance with ethical research standards.
Provided support during clinic visits, sample collection, and post-vaccination monitoring, ensuring smooth participant engagement
A highly organized and detail-oriented professional with diverse experience across clinical research, healthcare, education, and administrative support roles. Proven success in managing clinical trial documentation, coordinating with multidisciplinary teams, and ensuring compliance with regulatory standards. Demonstrated ability to adapt quickly, support team operations, and maintain high-quality service delivery in both clinical and non-clinical settings.
Experienced in coordinating patient care, supporting service delivery, and ensuring smooth operational processes in both research and healthcare environments.
Hold a Master's degree in Pharmaceutical Science with Management from Kingston University, UK, enhancing scientific knowledge with leadership and operational skills. Also qualified with a Doctor of Pharmacy (Pharm D) from India, providing a solid foundation in pharmacology, patient care, and medical ethics. Academic background includes practical research experience, with a published project in the Indian Journal of Pharmacy Practice.
