Regulatory Submissions jobs
4 open roles for regulatory submissions, updated continuously as employers post them.
Senior Medical Writer
A senior medical writing role at argenx, authoring clinical and regulatory documents for autoimmune disease drug programs. Suits a medical writer with 3+ years of sponsor-level pharma or biotech regulatory writing experience, based in the US.
Patient Safety Associate I (Drug Safety Associate I)
A fully remote, US-based entry-level pharmacovigilance role processing safety case reports and supporting regulatory submissions.
Regulatory Consultant (Veeva RIM)
Syneos Health is hiring a remote Regulatory Consultant in Ontario to coordinate life sciences submissions and maintain regulatory plans in Veeva Vault RIM. The role suits a regulatory-affairs professional with at least three or five years of submissions experience, depending on degree level.
Senior Submissions Officer
A senior pharmacovigilance submissions role at PrimeVigilance in Raleigh, NC, managing safety report submissions for pharmaceutical clients.