Job Summary:
We are seeking an experienced Medical Writer to join our global team. As a Medical Writer, you will play a key role in preparing high-quality clinical study reports and protocols for Phase I-III interventional studies.
* Take the lead in preparing assigned documents, confirming scope of task, templates and specifications, negotiating timelines, organizing document reviews and communicating with customers.
* Manage day-to-day workload by identifying project needs, tracking timelines and implementing customer requests while keeping managers informed about progress on tasks and any potential issues.
* Liaise with customers independently via meetings or presentations to discuss templates results lessons learned etc
You will have extensive experience as a lead writer in preparing CSRs and protocols with consistently positive feedback from customers and colleagues. You must be proficient in Japanese is not required but would be beneficial. Good understanding of common statistical methods used in clinical trials interpretation of their results data integration summation medical terminology across various therapeutic areas necessary for this role also preferred excellent written oral communication skills attention to detail accuracy judgment independence collaboration ability to establish maintain working relationships effectively manage multiple tasks projects proactively identify risks solutions raise them appropriately senior guidance input computer literacy are all essential qualities sought after candidates that meet these requirements can thrive find challenging stimulating careers within our company they involve connecting people science advance healthcare outcomes worldwide through efforts being conducted around globe every single one contributes shared goal improving lives patients everywhere no matter roles everyone at IQVIA crucial element success giving back thanks interest growing career us -