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Regulatory Affairs Specialist Small Molecule

Remote • Posted 2 hours ago • Updated 2 hours ago

Contract W2

Contract Independent

Contract Corp To Corp

2 Years

No Travel Required

Remote

Depends on Experience

Fitment

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Job Details

Skills

Clinical Trials
Google Cloud
Google Cloud Platform
NDA
Regulatory Affairs
TMF
Veeva

Summary

Job Title: Clinical Regulatory Affairs Specialist – Small Molecule
Location: Remote

We are seeking a Clinical Regulatory Affairs Specialist with 9+ years of experience supporting small molecule clinical development programs.

Key Requirements:

Strong experience in Clinical Regulatory Affairs
Hands-on experience with Veeva Vault TMF or similar.
Experience with IND, CTA, and NDA submissions
Knowledge of ICH-Google Cloud Platform, FDA, EMA, and global regulatory requirements
Experience supporting clinical trials and collaborating with Clinical Operations teams
Strong regulatory documentation and inspection readiness experience.

Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.

Dice Id: jeanmart
Position Id: 9121582
Posted 2 hours ago

Contact the job poster

Vimal Jeeva

Sr. Recruitment Analyst @ Jean Martin, Inc

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