I am a Experienced clinical trial assistant in the pharmaceutical, biotechnology, and medical device industries. I have an exceptional ability to remain calm under pressure and effectively collaborate with diverse teams at all levels of a global organization. Skilled organizer experienced in developing and leading plans and procedures, particularly within chemistry and biology labs. Extensive experience shadowing doctors in surgical and ICU settings. I have a proven track record fostering community and managing facilities during challenging times, such as COVID-19. I am proficient in clinical trial management, specializing in oncology and vaccine research, with expertise in maintaining CTMS and providing support in study systems, site initiation, ensuring training compliance, query resolution, and overseeing sample shipments. Core competencies include:FDA Regulations | Good Clinical Practice / GCP | Vaccine Research | Electronic Trial Master File / eTMF | Microsoft Word | Microsoft Excel | Microsoft Office | Microsoft PowerPoint | Clinical Trial Management | Clinical Trial Monitoring | EMR / Electronic Medical Records | Data Management | Data Monitoring | Institutional Review Board / IRB | Site Management | eCRF | CRO / Clinical Research Organization | Clinical Development | Clinical Trial Management Systems / CTMS | Standard Operation Procedures / SOP | Detail Oriented | can be reached at Tallingham2018@gmail.com