I am looking for a skilled MEDICAL WRITER with experience in regulatory submissions, Phase 1 through 4 clinical study reports, regulatory submissions, investigator brochures, NDA documents
and more. Rare disease writing is a plus but you MUST have at least 3 years experience in oncology writing. You MUST have regulatory writing experience.
You must speak and write fluent English.
You must be available to go through a lengthy interview process (taking phone calls for interviews with various clients until you are hired)
You must be available to work regular US business hours
Once hired by a client you will be working full-time, 40+ hours per week on a permanent basis.
Add the word "REGULATORY" to the top of your response message, otherwise I will delete you.