Amanda Goode

Background

About Amanda Goode

Clinical/medical editor with a background in research working in the pharmaceutical industry since 2019. I am very detail oriented and deadline driven. I have experience performing QC of protocols/amendments, clinical study reports and associated narratives, investigator's brochures, informed consent/assent forms, periodic safety reports, clinical submission documents, and briefing books. Before transitioning to industry, I worked in academia, where I managed investigator-initiated studies, oversaw IRB submissions, researched funding opportunities, and edited and co-authored manuscripts and grant applications. Apart from editing and writing, my skills include mentoring and training new colleagues and developing guides and checklists to ensure consistency and quality of work within a group. please note: all opinions and views expressed are my own and not necessarily those of my employer.