Senior Medical Writer Jobs NEW JERSEY-CENTRAL
Exciting in-house medical writing opportunity located near Summit, NJ, seeks a team-oriented, experienced regulatory writer to lead the writing effort and work with senior management to set up document standards. Salary is excellent up to $115k plus a very attractive bonus. The group is very well-established with great career progression up for grabs!
We are searching for experienced writers specializing in Clinical Study Protocols, Clinical Study Protocol Amendments, Clinical Study Reports, Investigator brochures, Clinical Summaries and other documents, as needed.
Main job responsibilities include:
-Working NDA submission documents in eCTD format
-Write CSRs, protocols, IBs, and eventually higher level submission ready documents such as SCS, SCE, ISS ISE, clinical overviews, briefing books, etc.
-Help coordinate the efforts of the consultant writers and vendors
Requirements/Skills:
-More than 6 years of medical writing experience
-Minimum of B.S. degree
-Experience in leading NDA/BLA filings, EMEA filing experience a plus
-Great team player with some management experience
-Effective relationship and communication skills
This large pharmaceutical company pays extremely competitive compensation and a generous benefits package including stock incentives. Don't miss this opportunity to grow in a nurturing, dynamic, collaborative and energizing company environment!
Send Resumes to Dandan Zhu at Real Pharma, contact me today at 212-707-8499