Looking for a medical writer from late April to June/July 2018 to rewrite module 2.5 and 2.7 of an NDA as well as a new efficacy report. We are a consultancy that helps companies with their regulatory submissions. The writer will be working as part of the team which consists of a Regulatory Lead,Clinical Advisor and client.
Remote work OK. A little travel involved (kick off meeting, 1-2 team meetings).
If interested please create a profile on MEIRxRS - BioPharma Gigs website at http://biopharmagigs.meirxrs.com/ and submit.