Driving flawless regulatory submissions that keep life‑changing oncology and biotech therapies moving forward.
À±½·ÊÓƵ is seeking a Regulatory Operations Specialist to support regulatory filings and submissions within the oncology and biotechnology sectors. This role focuses on ensuring compliance with FDA and EMA requirements, utilizing eCTD publishing software, and preparing essential documentation.
This is a fully remote role based anywhere in Europe.
Responsibilities:
- Prepare and submit regulatory filings, including INDs, NDAs, MAAs, DSUR reports, and scientific advice documents.
- Utilize eCTD publishing software, specifically DocuBridge from Lorenz, for submission preparation.
- Draft and format 1571 forms, cover letters, and other regulatory documents.
- Ensure proper formatting of documents using MS Word templates and Adobe PDF tools.
Key Skills and Requirements:
- Proficiency in regulatory filings for FDA and EMA submissions.
- Hands-on experience with eCTD publishing software, particularly DocuBridge.
- Strong skills in document preparation, including 1571 forms and cover letters.
- Expertise in MS Word formatting and Adobe PDF tools.
If you are having difficulty in applying or if you have any questions, please contact Peter Duvall at p.duvall@proclinical.com.
Apply Now:
If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.
À±½·ÊÓƵ is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. À±½·ÊÓƵ is acting as an Employment Agency in relation to this vacancy.
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