Clinical Research Professional – Ethics and Regulatory Affairs Astute and detail-oriented professional with 6-years of experience conducting research and clinical trials, utilising different methodologies as well as a strong commitment to improving processes and project management. I am enthusiastic about leveraging my research expertise in oncology, clinical experience, knowledge translation, strategic planning, and relationship-building skills to contribute to cancer research and achieve research project goals within budget and deadlines. Relevant Skills Excellent verbal and written communicator. Excellent knowledge of medical terminology, PHIA and hTCP2: CORE certified Collaborating with a multi-disciplinary team. Proven attention to accuracy and detail in disseminating study and regulatory information to team members. Proficient in Microsoft Office and Internet. Excellent knowledge of ICH-GCP and ethics in clinical research. Proficient in data management using appropriate software such as REDCAP. Adaptable to learning new skills and software. Detail-oriented Clinical Research Associate well-versed in coordinating operations, managing sites and drafting detailed clinical reports. Knowledgeable about action planning, database locking and standard operating procedures. Supports participant recruitment and management to meet research objectives.
▪ Nature enthusiast with a passion for baking (I love carrot cake!) and the culinary arts.