I am a dedicated and detail-oriented Research Associate with a Master's degree in Applied Microbiology and a diploma in Clinical Research. My professional journey has equipped me with a solid foundation in microbiological research, clinical sample processing, and robust data management. With hands-on experience in customer support, I excel in communication, collaboration, and problem-solving.In my current role, I work on projects primarily focused on cancer and surgical oncology. I coordinate sample collection and processing schedules, ensuring the highest quality control standards. I liaise with clinical staff and patients, manage data meticulously, and contribute to the development of laboratory protocols and procedures. Additionally, I counsel patients for informed consent, fill case report forms (CRFs), and manage extensive data sets, ensuring accuracy and compliance with regulatory standards.Driven by a passion for improving patient safety and public health, I am now seeking to transition into a long-term career in pharmacovigilance. I am eager to leverage my scientific expertise, clinical research experience, and customer support skills to monitor, assess, and prevent adverse drug reactions, ultimately contributing to the safe and effective use of medications.I am enthusiastic about the opportunity to join a dynamic pharmacovigilance team where I can continue to grow professionally and make a meaningful impact on patient care and drug safety.