Senior Regulatory Affairs Associate - Generalist
Employment type
Full-time
Work setting
On-site
Location
Sacramento, CA
Schedule
Day shift
Posted
You'll be redirected to the employer's application page.
Job overview
The Senior Regulatory Affairs Associate - Generalist is an onsite role based in Sacramento, CA. Compensation is not specified. This role supports a strategic pharmaceutical partnership. This role exists to provide end-to-end regulatory affairs support for partnered assets. The associate works with internal and external stakeholders to ensure regulatory excellence across clinical, submission, and post-approval activities.
What you'll do
- Maintain regulatory archive logs
- support clinical regulatory documentation
- draft submission components
- collaborate with Global Regulatory Teams
- prepare post-marketing reports.
What we're looking for
- Skills & competencies
- full-timeday shiftsacramento caregulatory affairspharmaceuticalcompliancedocumentationonsiteclinicalsubmission
- Work arrangement
- Weekend coverage required
Why this role
Requires 3+ years of regulatory affairs experience.
About the employer
Parexel is hiring for this role. Industry: Administrative Management and General Management Consulting Services. Sector: 54.
Additional details
- Industry sector
- 54
- Industry
- Administrative Management and General Management Consulting Services
- Occupation code
- 13-1041.07
You'll be redirected to the employer's application page.
Listing ID: 4eb20b75-fe4e-48b5-bc94-1d027b2b1849