Regulatory Affairs Consultant - CMC (Biological / vaccines)
Parexel
About this role
The Regulatory Associate Consultant is responsible for authoring and managing global CMC regulatory submissions, ensuring compliance with international regulatory requirements, and supporting the development and review of CMC packages. They work closely with stakeholders to facilitate regulatory processes in the biotech or pharmaceutical industry.
Skills
Qualifications
About Parexel
parexel.comFor over 35 years Parexel has been a trusted global CRO and biopharmaceutical services company. Learn more about how we can help.
Recent company news
Strauss Borrelli PLLCParexel Data Breach Investigation
Dec 17, 2025
GlobeNewswireParexel Named “Best Contract Research Organization” at 21st Annual Scrip Awards
Dec 12, 2025
ClassAction.orgParexel Data Breach Exposes SSNs, Financial Info; Lawyers Investigate
Dec 18, 2025
Business North CarolinaUpdate: How 7 companies delivered on NC job promises
1 month ago
Yahoo FinanceParexel Establishes New Global Headquarters in Raleigh’s North Hills Innovation District
Sep 9, 2025
About Parexel
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 Parexel.
Salary
$120k – $160k
per year
More jobs at Parexel
Similar Jobs
Associate Manager CMC Regulatory Affairs
Regeneron Pharmaceuticals
Regulatory Affairs Specialist III
Arcotech
Global Regulatory Affairs (CMC) Manager
Integrated Resources INC
Global Regulatory Affairs (CMC) Manager
Integrated Resources INC
Manager Regulatory Affairs-CMC
Integrated Resources INC
Associate Regulatory Affairs
Dr Reddy's Laboratories Limited