Pharmaceutical Regulatory Affairs
October 18, 2007 6:26 AM
My firm has been engaged to expand the capacity of the Regulatory Affairs department for an innovative biotechnology firm on Canada's beautiful west coast.
We are looking for experienced, skilled RA professionals to manage the regulatory approvals process for Canada and the United States as the company moves several drug candidates through the final stages of clinical development.
There are opportunities at the Associate Director level as well as less senior positions for submissions specialists and CMC regulatory associates. Candidates should have significant experience with regulatory submissions to the FDA and TPD (e.g., INDs, NDAs, annual reports, IND amendments, NDA supplements, routine correspondence). Experience with electronic submissions will be especially valuable.
Detailed job descriptions are available upon request.
payscale: Competitive and commensurate with experience
job type: full-time
We are looking for experienced, skilled RA professionals to manage the regulatory approvals process for Canada and the United States as the company moves several drug candidates through the final stages of clinical development.
There are opportunities at the Associate Director level as well as less senior positions for submissions specialists and CMC regulatory associates. Candidates should have significant experience with regulatory submissions to the FDA and TPD (e.g., INDs, NDAs, annual reports, IND amendments, NDA supplements, routine correspondence). Experience with electronic submissions will be especially valuable.
Detailed job descriptions are available upon request.
payscale: Competitive and commensurate with experience
job type: full-time
This job has been filled.