Lilly seeks an experienced medical writer to lead planning, authoring, and review of complex clinical and regulatory documents across development programs, collaborating with clinical development, regulatory affairs, biostatistics, medical affairs, and legal to ensure scientific accuracy and regulatory compliance.
The ideal candidate holds a bachelor’s degree in a scientific field (Master’s or PhD preferred) and at least eight years of medical writing experience in pharma/biotech/CRO, with
#J-18808-LjbffrAssociate Director, Medical Writing & Regulatory Strategy in boston at Unknown Company
This position is listed as full time and onsite.