Farwaniya, Kuwait
Biotechnology engineer with over 4.5 years of experience, including 3 years in pharmacovigilance and 1.6 years as a Clinical Research Associate. With a deep passion for healthcare, I specialize in ensuring quality and compliance across projects, focusing on strategic metrics and solutions. My diverse experience has equipped me with the ability to navigate complex challenges and contribute effectively to the success of every initiative I’m part of.
Receive, triage, review and process Lifecycle Safety data from various sources on time, with quality standards. Perform data entry for tracking and Lifecycle Safety databases, coding relevant medical terminology, writing descript narratives, generating queries pertinent to the case, performing quality control, assisting with reconciliation, driving case closure, coordinating translations and ensuring reports are sent to the customer within assigned deadlines. Mentored less experienced or newer staff members. Handles multiple clinical trial project.