Back to search

Senior Regulatory Affairs Associate (Generalist)

Parexel · Richmond, VA · Regulatory Affairs

Employment type

Full-time

Work setting

On-site

Location

Richmond, VA

Schedule

Day shift

Posted

Apply for this job

You'll be redirected to the employer's application page.

Job overview

The Senior Regulatory Affairs Associate (Generalist) is an onsite role based in Richmond, VA. Compensation is not specified for this position. This role supports a strategic pharmaceutical partnership. This position provides end-to-end regulatory support for partnered assets. The associate manages documentation, submission execution, and compliance with global regulatory requirements across clinical and post-approval activities.

What you'll do

  • Maintain regulatory archive logs.
  • Author 1572 waiver requests.
  • Draft administrative components of submissions.
  • Prepare materials for Global Regulatory Team meetings.
  • Support post-marketing regulatory reports.

What we're looking for

Skills & competencies
full-time
day shift
richmond va
regulatory affairs
pharmaceutical
onsite
compliance
documentation
submission
generalist
Work arrangement
  • Weekend coverage required

Why this role

Eastern/Central time zone preference.

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
11-9199.01
Apply for this job

You'll be redirected to the employer's application page.

Browse more jobs

Listing ID: f1602c76-89b3-4abe-b6d8-a92dcfb84a5d

    Senior Regulatory Affairs Associate (Generalis… | CollabWORK