MMS Holdings Inc is seeking a Medical Writer to evaluate literature, design studies, and prepare regulatory documents for clinical development. You will author or co-author protocols, reports, consent forms, and safety summaries, while meeting tight timelines and maintaining document quality.
The ideal candidate has 3+ years in pharmaceutical regulatory writing and strong leadership skills, with advanced MS Word, Excel, and PowerPoint proficiency.
#J-18808-LjbffrSenior Medical Writer – Regulatory Submissions & Study Lead in new york at Unknown Company
This position is listed as full time and onsite.