Pharmacovigilance Specialist, Submissions
ProPharma
About this role
The Pharmacovigilance Specialist, Submissions at ProPharma supports pharmacovigilance regulatory reporting and submission compliance for biotech, medical device, and pharmaceutical clients using a multi-tenant Argus environment. The role helps ensure adherence to reporting processes, periodic safety reporting requirements, and submission testing to maintain compliance with health authorities and safety partners.
Skills
Qualifications
About ProPharma
propharmagroup.comProPharma helps navigate the complexities of drug development and ensure patient health and safety throughout the product lifecycle.
Recent company news
ProPharma Expands Operations with New Office in Hyderabad
Dec 11, 2025
ProPharma's award-winning strategic acquisition and expansion
Sep 24, 2024
New global headquarters for ProPharma coming to downtown Raleigh
Apr 12, 2023
ProPharma relocates Overland Park headquarters to North Carolina
Apr 25, 2023
ProPharma Group and The Planet Group Announce Executive Leadership Changes and Branding of Combined Company
Sep 9, 2023
About ProPharma
Headquarters
San Francisco, CA
Company Size
201-500 employees
Founded
2018
Industry
Technology
Glassdoor Rating
4.2 / 5
Leadership Team
Sarah Johnson
Chief Executive Officer
Michael Chen
Chief Technology Officer
Emily Williams
VP of Engineering
David Rodriguez
VP of Product
Jessica Thompson
Chief Financial Officer
Andrew Park
VP of Sales
Unlock Company Insights
View leadership team, funding history,
and employee contacts for ProPharma.
Salary
$117k – $156k
per year
More jobs at ProPharma
Similar Jobs
Director, Pharmacovigilance Intake and Regulatory Submissions
Regeneron Pharmaceuticals
Pharmacovigilance Specialist (Submissions specialist) Taiwan
Biomapas
Safety Science Coordinator I
Fortrea
Pharmacovigilance Manager, Aggregate & Trend Reports
American Regent
Graduate Pharmacovigilance Associate
ICON plc
Pharmacovigilance Associate
ICON plc