Regulatory Affairs Associate — Remote/Hybrid, Global Submissions

4D Molecular Therapeutics; Emeryville (CA); Hybrid; USD 50,000 - 54,000; Full time

Job summary

4D Molecular Therapeutics is seeking a Regulatory Affairs Associate to support the Regulatory Project Team in advancing product pipeline toward regulatory approval and commercialization. The role collaborates with internal and external stakeholders to ensure timely review and approval of submissions.

The position offers remote or hybrid work options with a strong preference for candidates in the SF Bay Area/West Coast.

Qualifications

• Bachelor’s degree in a relevant field required.
• Advanced certificate or degree a plus.

Responsibilities

• Draft and format regulatory submissions.
• Coordinate cross-functional deliverables (CMC, nonclinical, clinical).
• Schedule submissions and maintain regulatory dashboards and timelines.
• Prepare documents for Health Authority interactions.

Skills

Communication skills

Team player

Prioritization

Attention to detail

Written communication

Regulatory knowledge

Education

Bachelor’s degree in a relevant field

Advanced certificate or degree a plus

Tools

Microsoft Word

Outlook

SharePoint

Adobe Acrobat

Job description

4D Molecular Therapeutics is seeking a Regulatory Affairs Associate to support the Regulatory Project Team in advancing product pipeline toward regulatory approval and commercialization. The role collaborates with internal and external stakeholders to ensure timely review and approval of submissions.

The position offers remote or hybrid work options with a strong preference for candidates in the SF Bay Area/West Coast.