IQVIA in the United Kingdom (Cambridge) is seeking a Senior Medical Writer to lead the development of clinical and regulatory documents for global submissions, including IBs, CSRs, and MAAs/NDAs. You will serve as the lead writer for key summaries and coordinate across multiple programs with Clinical, Regulatory Affairs, Biostatistics, and Safety.
The role requires a strong background in medical writing, 5+ years of experience, and comprehensive knowledge of ICH, FDA, and EMA guidelines.
#J-18808-LjbffrSenior Medical Writer – Global Regulatory Lead (FSP) in Cambridge employer: IQVIA
IQVIA in Livingston, Scotland is an excellent employer that fosters a collaborative team environment and prioritises employee growth through outstanding career development opportunities. Working as a Lab Operations Assistant here not only allows you to contribute to meaningful projects but also ensures you are part of a supportive workplace that values safety and professionalism.
