MMS Holdings Inc is seeking a skilled Medical Writer to join our regulatory writing team. The role focuses on evaluating literature, developing clinical development documents, and ensuring scientific rigor under regulatory timelines.
The ideal candidate has 3+ years in pharmaceutical regulatory writing, strong MS Word/Excel/PowerPoint skills, and experience leading document production for submissions to authorities.
#J-18808-LjbffrSenior Medical Writer & Project Lead in Remote at Unknown Company
This position is listed as full time and onsite.